FAQ
印刷
Bookmark
シェア
more..
You are not authorized to download the resource
Sort options
アルファベット順
関連順
関連順
How many transfections can I perform with 20 nmol of HPP grade siRNA?
FAQ ID -367
表示
How do I submit a siRNA order by telephone or online?
FAQ ID -399
表示
What is the white insoluble precipitate in my resuspended plasmid DNA pellet?
FAQ ID -352
表示
What kits does QIAGEN offer to extract RNA from whole blood?
FAQ ID -304
表示
Why do I get genomic DNA contamination in my plasmid prep?
FAQ ID -353
表示
Which primers can I use for sequencing pQE-expression vector constructs?
FAQ ID -343
表示
What is the standard assay volume recommended for LiquiChip assays?
FAQ ID -330
表示
What is the average molecular weight of a siRNA, and how do I convert uM to ug values?
FAQ ID -388
表示
What are the dissociation constants for the Anti-His Antibodies?
FAQ ID -385
表示
What is the lowest elution volume that can be used with QIAprecipitator Midi and Maxi Modules?
FAQ ID -307
表示
What is the origin of replication and the plasmid copy number of the pQE vectors?
FAQ ID -338
表示
What is the acceptable maximum g force for centrifugation of Xa Removal Resin?
FAQ ID -320
表示
What is the composition of Buffer FG3?
FAQ ID -356
表示
What is the composition of PBS?
FAQ ID -361
表示
How can I keep my centrifuge tubes endotoxin-free?
FAQ ID -301
表示
Can I use ethanol instead of isopropanol for DNA precipitation when using HiSpeed Plasmid Kits?
FAQ ID -354
表示
303 - Can I use my own lysis buffer with the DNeasy Blood & Tissue or QIAamp DNA Mini Kit?
表示
Can I store agarose gel slices containing DNA for gel extraction at a later point?
FAQ ID -313
表示
Can I use a partial MinElute 96 UF plate?
FAQ ID -355
表示
Can I use the RNeasy Mini Kit or RNeasy 96 Kit with fewer than 100 cells?
FAQ ID -372
表示
Can I use water for elution from the QIAprecipitator of the HiSpeed Plasmid Kits?
FAQ ID -306
表示
Are QIAprep and QIAquick Spin columns interchangeable?
FAQ ID -311
表示
Are the QIAprecipitator Midi and Maxi Modules of the HiSpeed Plasmid Kits interchangeable?
FAQ ID -308
表示
Apart from the antibody itself, does the Penta-His Biotin Conjugate solution contain any protein?
FAQ ID -359
表示
Are QIAGEN monoclonal Anti His Antibodies glycosylated?
FAQ ID -334
表示
Can I eliminate RNase A from buffer P1 for my plasmid preparation to obtain RNase-free DNA for in-vitro transcription?
FAQ ID -366
表示
Can I perform in-vitro transcription with the pDrive Cloning Vector from the QIAGEN PCR Cloning Kit?
FAQ ID -332
表示
Can Buffers N3 and P3 be used interchangeably?
FAQ ID -310
表示
Do the QuantiTect SYBR Green Kits contain a stabilization reagent that inhibits the sensitivity of real-time PCR?
FAQ ID -328
表示
How are siRNAs introduced into C. elegans?
FAQ ID -396
表示
Do I need to anneal, deprotect or desalt my QIAGEN siRNA?
FAQ ID -398
表示
Do pQE vectors contain the CAT gene?
FAQ ID -362
表示
How can I improve DNA yields from very tough tissues using the DNeasy Blood & Tissue Kit or the QIAamp DNA Mini Kit?
FAQ ID -374
表示
How can I improve the expression of proteins containing hydrophobic regions?
FAQ ID -339
表示
How can I check if any residual proteins remain on the Ni-NTA Agarose matrix after elution?
FAQ ID -324
表示
How can I express toxic protein in E. coli?
FAQ ID -373
表示
Do freeze-thaw cycles affect the stability of the U-overhang on the pDrive Cloning Vector?
FAQ ID -323
表示
Can RNAprotect Tissue Reagent be used to store previously isolated RNA?
FAQ ID -337
表示
Can MinElute 96 UF PCR be used to purify PCR samples which contain mineral oil?
FAQ ID -360
表示
Can siRNA silence bacterial genes?
FAQ ID -395
表示
Does SYBR Green dye present in QuantiTect kits interfere with ethidium bromide staining?
FAQ ID -312
表示
Does the 5x OneStep RT-PCR Buffer contain BSA?
FAQ ID -326
表示
Do any of the buffers in the HotStarTaq DNA Polymerase Kit contain Triton?
FAQ ID -327
表示
Do any of the kit components or the product packaging of the QIAamp 96 DNA Blood Kit contain latex?
FAQ ID -318
表示
What are exo-resistant random hexamers used in the REPLI-g reaction?
FAQ ID -710
表示
The Sigma Centrifuge makes a loud noise at low speeds which disappears at higher speeds, when using the 2x96-well plate rotor. What is the problem?
FAQ ID -776
表示
Is RNAprotect Bacteria Reagent compatible with the RNeasy Mini Kit?
FAQ ID -797
表示
What is the average DNA concentration obtained using the DirectPrep 96 Miniprep Kit?
FAQ ID -721
表示
What are the expected average DNA yields from plant extractions on the BioSprint 96?
FAQ ID -771
表示
What is the basic technology behind the Strep-tag Protein Purification System?
FAQ ID -740
表示
What is the advantage of running an analytical gel with fractions of my plasmid preparation?
FAQ ID -769
表示
What can be used as an alternative to the A260 measurement for quantification of small amounts of RNA and DNA?
FAQ ID -728
表示
I bound an 11 kb DNA fragment to a QIAquick column; is it completely lost?
FAQ ID -756
表示
If template abundance differs significantly between housekeeping and target gene, are both amplified equally efficient with the QuantiTect Multiplex Kits?
FAQ ID -718
表示
How to quantitate DNA purified using the BioSprint 96?
FAQ ID -773
表示
How to store DNA from forensic samples eluted into water on the EZ1 biorobot in TE buffer instead?
FAQ ID -734
表示
I accidentally stored Buffer RDD of the RNase-Free DNase Set at°C. Will it still function?
-20
表示
Is it possible to use LiquiChip beads for FACS applications?
FAQ ID -733
表示
Is it possible to use the QuantiTect Reverse Transcription Kit with bacterial RNA?
FAQ ID -785
表示
I ran my RNA out on an agarose gel and can see lots of bands similar to a ladder. Why?
FAQ ID -745
表示
Is GFP excited and detected by the green laser of the LiquiChip System?
FAQ ID -737
表示
Is it possible to buy the EZ Competent Cells of the QIAGEN PCR Cloning Plus Kit separately?
FAQ ID -763
表示
Which Qproteome or Protein Fractionation Kits from QIAGEN are compatible with tissue samples?
FAQ ID -755
表示
Why are some of my RNAprotect-stabilized samples frozen atºC while others are not?
ID -758
表示
Where can I find info on compatible reporter dyes for use in real-time multiplex PCR using the QuantiTect Multiplex PCR Kits?
FAQ ID -719
表示
Why are the QuantiTect and QuantiFast Multiplex PCR Kits limited to triplex real-time PCR on some cyclers?
FAQ ID -715
表示
Why might my gene of interest drop out during WGA if it is not near a telomere or centromere?
FAQ ID -703
表示
Will the random hexamers in the REPLI-g reaction interfere with downstream analysis?
FAQ ID -713
表示
Why should DNA or cDNA targets be less than 250 bp long for real-time PCR?
FAQ ID-751
表示
Why is my plasmid DNA yield low?
FAQ ID -768
表示
What is the difference between Ni-NTA Agarose and Ni-NTA Superflow?
FAQ ID -764
表示
What is the difference between QIAGEN Protease and QIAGEN Proteinase K provided in various QIAamp Kits?
FAQ ID -761
表示
Why is there no detection of free reporter fluorescence in the LiquiChip System?
FAQ ID -732
表示
What is the composition of buffer AE?
FAQ ID -730
表示
What is the cell number range one can use with the FastLane Cell cDNA Kit for real-time RT-PCR?
FAQ ID -782
表示
What is the composition of Buffer N3?
FAQ ID -767
表示
What negative (unphosphorylated) and positive (phosphorylated) control proteins do you recommend for use with the PhosphoProtein Purification Kit?
FAQ ID -779
表示
Where can I find a copy of the report files generated by running accessory protocols "Dilutor Delivery (monthly)" and "High-Speed Pipetting Sytem (monthly)" on my BioRobot 9604?
FAQ ID -766
表示
What type of Sequencing Services does QIAGEN offer?
FAQ ID -781
表示
What is the enzyme used in the REPLI-g reaction?
FAQ ID -704
表示
What is the recipe for SOC medium?
FAQ ID -798
表示
What is the general sensitivity level of the LiquiChip System?
FAQ ID -731
表示
How should fluorescent labeled probes be stored?
FAQ ID -784
表示
Can QIAGEN's Taq- and HotstarTaq DNA Polymerases be used for cycle sequencing?
FAQ ID -741
表示
Can RNAprotect Tissue Reagent be used to stabilize tissue which has already been flash-frozen?
FAQ ID -757
表示
Can I use the PhosphoProtein Purification Kit to purify phosphorylated peptides of around 1 kD size?
FAQ ID -778
表示
Can lyophilized plant material be used for DNA extraction on the BioSprint 96?
FAQ ID -772
表示
Can I use the QuantiTect Multiplex PCR Kits on the Roche LightCycler systems with TaqMan® probes or QuantiTect Assays?
FAQ ID -717
表示
Can the REPLI-g WGA enzyme work with labeled dNTPs?
FAQ ID -706
表示
Does the QIAamp DSP Virus Kit require the QIAvac 24 Plus, or can I use it with my own laboratory vacuum system?
FAQ ID -789
表示
Can the MAPK1 siRNA of the RNAi Human/Mouse Starter Kit be purchased separately?
FAQ ID -744
表示
Can the QIAprep Spin Miniprep Kit be used for isolating plasmid DNA from mammalian cells?
FAQ ID -795
表示
Can the QIAvac 96 vacuum manifold be used with DirectPrep 96 plates?
FAQ ID -722
表示
Are the buffers in the Ni-NTA Fast Start Kit the same as the ones for use with Ni-NTA purchased separately?
FAQ ID -791
表示
Are the protocols from the BioSprint software compatible with the KingFisher software and vice versa?
FAQ ID -770
表示
Are Buffer PB of the QIAquick PCR Purification Kit and Buffer QG of the QIAquick Gel Extraction Kit interchangeable?
FAQ ID -786
表示
Any data on the fidelity of the REPLI-g MDA technique?
FAQ ID -707
表示
Are Centromeres and Telomeres amplified using REPLI-g WGA?
FAQ ID -702
表示
Can I use my own primers for REPLI-g WGA to amplify a specific chromosomal region?
FAQ ID -712
表示
Can I use REPLI-g for SNP Genotyping?
FAQ ID -700
表示
Can I do 4-plex real-time PCR, on the ABI PRISM 7000, 7700, or 7900 using the QuantiTect Multiplex PCR Kit?
FAQ ID -716
表示
Can I purchase Phi29 DNA polymerase only?
FAQ ID -708
表示
How can I get specific information and a quote for my individual Sequencing Service needs?
FAQ ID -792
表示
How can one perform multiplex real-time PCR analysis using the LightCycler 2.0?
FAQ ID -780
表示
How can I be sure that I am harvesting my induced bacterial culture at the best time point for protein expression?
FAQ ID -788
表示
How can I get a certificate for quality assurance (ISO 13485 and ISO 9001) from QIAGEN?
FAQ ID -762
表示
How do the FastLane Cell cDNA Kit and QuantiTect Reverse Transcription Kit eliminate genomic DNA contamination?
FAQ ID -783
表示
How many cells can be used with the FastLane Cell cDNA Kit?
FAQ ID -796
表示
Do you have an antibody for Western Blot Analysis of MAPK1 gene knockdown using your MAPK1 control siRNA?
FAQ ID -746
表示
Do I have to switch off the laser of the LiquiChip Workstation overnight?
FAQ ID -736
表示
Can frozen blood be used for whole genome amplification with REPLI-g?
FAQ ID -794
表示
How many reporter dyes can be used in the same analysis using the LiquiChip Workstation?
FAQ ID -738
表示
How much DNA is obtained in the average PCR reaction?
FAQ ID -750
表示
Do I need to determine limiting primer concentrations with the QuantiTect Multiplex PCR Kits?
FAQ ID -714
表示
Do I need to have EDTA in the buffer in which I am going to store my isolated genomic DNA?
FAQ ID -754
表示
Do you synthesize thiophosphate modified random hexamers?
FAQ ID -711
表示
Has anyone verified whole genome amplification accuracy with Sequencing?
FAQ ID -701
表示
How best to handle the light sensitive LiquiChip reagents?
FAQ ID -735
表示
Do you have a protocol for the fixation of cells transfected with fluorescently labeled siRNA?
FAQ ID -793
表示
Do you have information about the cleanup of single-stranded DNA (ssDNA) with QIAquick columns?
FAQ ID -759
表示
Do you have information on the use of recombinant DNA and RNA as absolute standards for realtime RT-PCR?
FAQ ID -729
表示
Do you have a protocol for the isolation of genomic DNA from paraffin-embedded samples on the BioRobot M48?
FAQ ID -1019
表示
Is the TurboCapture Microplate Holder Type B compatible with the Biomek FX robotic workstation?
FAQ ID -1040
表示
How can I prevent running out of M48 Kit reagents before the full number of samples are processed?
FAQ ID -1042
表示
What are the additional plasmid bands I see on my gel?
FAQ ID -1059
表示
Is it possible to scale up QuantiTect Reverse Transcription reactions to allow use of larger amounts of RNA?
FAQ ID -1063
表示
Is it possible to use the PhosphoProtein Purification Kit in batch format?
FAQ ID -1069
表示
What are the recommended storage conditions for the QuantiTect Reverse Transcription Kit and its components?
FAQ ID -1077
表示
What is the difference between Buffers RLT and RLT Plus?
FAQ ID -1043
表示
What is the difference between TurboCapture Microplate Holders Type A and Type B?
FAQ ID -1038
表示
Is there a limit to the size of proteins that can be purified using the Qproteome Glycoprotein Kits?
FAQ ID -1071
表示
What blocking reagents do you recommend for chemiluminescent detection using Penta-, Tetra-, and RGS-His antibodies?
FAQ ID -1093
表示
Is Factor SB of the HotStar HiFidelity Polymerase Kit the same as Factor MP of the QIAGEN Multiplex PCR Kit?
FAQ ID -1049
表示
How can I transfect siRNA into insect cells such as Drosophila melanogaster S2?
FAQ ID -1046
表示
How can I tell TurboCapture Microplate Holder Type A from Type B?
FAQ ID -1039
表示
How much template can I use in the reaction and what is the maximum volume of template that can be used in the QuantiTect Kits?
FAQ ID -1086
表示
I am seeing a precipitate after adding LyseBlue reagent to Buffer P1. What should I do about that?
FAQ ID -1045
表示
How much dye-labeled siRNA should I use to monitor transfection efficiency when using HiPerfect Transfection Reagent?
FAQ ID -1058
表示
What is the error rate of HotStar HiFidelity DNA Polymerase?
FAQ ID -1048
表示
How do I perform an Acetone Precipitation for concentrating and desalting protein samples?
FAQ ID -1035
表示
Which kit should I use for RNA isolation from Cartilage?
FAQ ID -1026
表示
Which QIAGEN kit do you recommend for purifying plasmid DNA suitable for transfection of sensitive cells?
FAQ ID -1092
表示
Where can I find the serial number on QIAGEN's BioRobots?
FAQ ID -1064
表示
Which kit can be used for simultaneous purification of DNA and RNA from biopsies?
FAQ ID -1089
表示
Why does my PCR product show up later when comparing the QuantiTect SYBR Green PCR Kits with Roche kits using the same annealing temperature?
FAQ ID -1083
表示
Why is there RNA in the DNA eluate when using the AllPrep DNA Mini Spin Column?
FAQ ID -1044
表示
Will the "classic" RNeasy Mini Kit be discontinued after the launch of the Allprep DNA/RNA Mini Kit?
FAQ ID -1054
表示
Why does TA/UA cloning work with your proofreading HotStar HiFidelity DNA Polymerase?
FAQ ID -1053
表示
Why do melting temperatures differ between PCR fragments amplified with QIAGEN's QuantiTect SYBR Green PCR Kits and Roche Kits?
FAQ ID -1084
表示
Where can I find a protocol for cleanup of already purified plasmid DNA?
FAQ ID -1031
表示
What is the protein loading capacity per column of the Qproteome Albumin/IgG Depletion Kit?
FAQ ID -1090
表示
What is the largest PCR amplicon that can be amplified with the HotStar HiFidelity Polymerase Kit?
FAQ ID -1047
表示
What is the range of melting temperatures for the QuantiTect Primer Assay amplicons in the dissociation curve?
FAQ ID -1079
表示
What is the recipe for 1x PBS solution?
FAQ ID -1030
表示
What should I use as a standard for absolute quantification in real-time PCR?
FAQ ID -1085
表示
What vacuum pressure should be applied using the QIAvac 24 Plus for the QIAamp DSP Virus Kit and Blood Mini Kit Protocols?
FAQ ID -1033
表示
What is your recommendation for cleaning the TissueLyser Bead Dispenser (96-well format)?
FAQ ID -1055
表示
What is the resin in the Qproteome Murine Albumin and Qproteome Albumin/IgG Depletion Kits?
FAQ ID -1034
表示
What is the volume of the eluate when using either spin or vacuum procedures with the QIAprep 96 Turbo Miniprep Kit?
FAQ ID -1067
表示
How can I prevent clogging of QIAfilter cartridges?
FAQ ID -1060
表示
Do I have to discard Buffer RLT with beta-Mercaptoethanol (ß-ME) added to it after 1 month of storage?
FAQ ID -1037
表示
Do I have to use a ramp time of 2°C/sec on the LightCycler when using Quantitect Primer Assays?
FAQ ID -1065
表示
Does an activation time of 15 minutes influence the performance of the HotStarTaq Plus DNA Polymerase?
FAQ ID -1050
表示
Do I have to use CoralLoad Gel loading dye when using your HotStarTaq Plus DNA Polymerase?
FAQ ID -1052
表示
Do you have a protocol for the isolation of RNA from bacterial cultures using RNAprotect Bacteria Reagent and QIAzol Lysis Reagent?
FAQ ID -1020
表示
Do you have a protocol for the isolation of DNA from forensic samples using the BioRobot M48?
FAQ ID -1017
表示
Can the USB Port of the BioSprint 96 instrument be used to transfer programs from a PC to the instrument?
FAQ ID -1032
表示
Do you have a protocol for the isolation of DNA from mouse tails using MagAttract technology on BioRobot M96?
FAQ ID -1007
表示
Are your FlexiTube siRNAs preferentially designed to any particular region of the target gene?
FAQ ID -1091
表示
Are the CoralLoad dyes in the HotStarTaq Plus PCR Buffer visible when loading small amounts of PCR product onto a gel?
FAQ ID -1051
表示
Are the new EZ1 RNA Kits (cat. no. 958034; 959034; 956034) compatible with the previous EZ1 RNA Card (cat. no. 9015590) or EZ1 RNA Universal Tissue Card (cat. no 9016384)?
FAQ ID -1025
表示
Can PCR fragments generated with the EasyXpress Linear Template Kit be cloned into the pIX4.0 vector of the EasyXpress Protein Synthesis Insect Kit?
FAQ ID -1078
表示
Can the QProteome O-Glycan Glycoprotein Kits be used for blood cells?
FAQ ID -1036
表示
Can the Reverse Transcriptases of the QuantiTect Reverse Transcription Kit and the QuantiTect Probe RT-PCR Kit be used interchangeably?
FAQ ID -1066
表示
Can the AllPrep RNA/Protein Kit be used with tissue?
FAQ ID -1095
表示
Can the Blocking Reagent supplied with the Penta-His HRP Conjugate be used with other antibodies?
FAQ ID -1073
表示
Do you recommend 1-step or 2-step real-time RT-PCR for gene expression analysis?
FAQ ID -1056
表示
How can I check for purity of RNA isolated using RNeasy Kits?
FAQ ID -1023
表示
How can air bubbles in PhosphoProtein Purification Columns be avoided?
FAQ ID -1070
表示
How can I increase low-copy plasmid DNA yields using QIAfilter Plasmid Kits?
FAQ ID -1062
表示
How can I increase DNA concentration using QIAprecipitators of the HiSpeed Plasmid Kits?
FAQ ID -1061
表示
How can I check the integrity of RNA purified using RNeasy Kits?
FAQ ID -1024
表示
How can I ensure complete genomic DNA removal when using the RNase-Free DNase Set?
FAQ ID -1087
表示
Do you have information on the reproducibility of DNA yields from blood using the M48 BioRobot?
FAQ ID - 1004
表示
Do you have a protocol for transient transfection of HeLa-S3 cells in 60 mm dishes using PolyFect?
FAQ ID -1012
表示
Do you have a protocol for transient transfection of HEK 293 cells in 75 cm3 flasks?
FAQ ID -1014
表示
Do you have a protocol for transient transfection of cells in 96-well plates using PolyFect Transfection Reagent?
FAQ ID -1013
表示
Do you have a protocol for the isolation of total nucleic acids from cells on the M48 BioRobot?
FAQ ID -1009
表示
Do you have a protocol for the isolation of total nucleic acids from tissue on the M48 BioRobot?
FAQ ID -1008
表示
Do you have a protocol for vacuum processing of blood samples with the QIAamp DNA Blood Midi or Maxi Kits?
FAQ ID -1011
表示
Do you have information on realtime RT-PCR performance of RNA isolated from monocytes on the M48 BioRobot?
FAQ ID -1010
表示
Do you have information on PCR template preparation from preserved blood samples on the M48 BioRobot?
FAQ ID - 1003
表示
Do you have information on DNA yields from blood with variable numbers of white blood cells using the M48 BioRobot?
FAQ ID -1006
表示
What Disinfectant Solution do you recommend for the BioRobot MDx?
FAQ ID -809
表示
What data documentation does QIAGEN's Sequencing Service provide for customers?
FAQ ID -832
表示
What are the sequences of the FlexiTube siRNAs?
FAQ ID -851
表示
What annealing temperature should be used with the QuantiTect Primer Assays?
FAQ ID -849
表示
What is the proper way to turn on or turn off the EZ1 instrument?
FAQ ID -870
表示
My BioRobot 9604 came with several Accessory Applications. Is it recommended I run these protocols?
FAQ ID -872
表示
What is the Energy Mix in the EasyXpress Kits?
FAQ ID -846
表示
What is the concentration of the primers in a reaction using the QuantiTect Primer Assays?
FAQ ID -850
表示
I would like to sequence my siRNA constructs. Does QIAGEN offer Sequencing Services for cloned siRNA?
FAQ ID -829
表示
Is it possible to perform immunoprecipitation (IP) directly on protein fractions from the Qproteome Cell Compartment Kit?
FAQ ID -855
表示
Is it possible to use frozen cell pellets with the FastLane Cell cDNA Kit?
FAQ ID -835
表示
Is it possible to elute plasmid DNA from the QIAprep Spin Miniprep columns with buffer containing Potassium Phosphate?
FAQ ID -854
表示
Is it possible to adjust the Lysis Buffer volume used with the Qproteome Bacterial Protein Preparation Kit?
FAQ ID -841
表示
Is it possible to use QIAGEN's pQE-TriSystem Vectors with the EasyXpress Protein Synthesis Insect Kit?
FAQ ID -876
表示
Is there a stopping point in the protocol for Suspended Cells using the FastLane Cell cDNA Kit?
FAQ ID -837
表示
Is the random biotin labeling of proteins expressed with your EasyXpress Biotin Labeling Kit as sensitive as labeling with radioactivity?
FAQ ID -875
表示
Is the E. coli Host Strain M15[pREP4] resistant to Zeocin?
FAQ ID -842
表示
Will acetone precipitation recommended in the Qproteome Protocols denature Protein?
FAQ ID -807
表示
Will biotin detection assays be efficient when doing in vitro translation from E. coli lysates with the EasyXpress Site-Specific Biotin Kit?
FAQ ID -878
表示
Why would clumps occur following the addition of Buffer P2 when using LyseBlue Reagent in a plasmid preparation?
FAQ ID -862
表示
Why is it recommended to add 1 mM IPTG for optimal protein yields using the EasyXpress Protein Synthesis Kits?
FAQ ID -860
表示
With LyseBlue reagent for lysis control, can I now process more bacterial culture and overload the columns?
FAQ ID -864
表示
Will site-specific biotin labeling with the EasyXpress Site-Specific Biotin kit alter the structure and function of my protein?
FAQ ID -877
表示
Will the sequences of the QuantiTect Primer Assays be provided?
FAQ ID -804
表示
Which resin is used in the QIAexpress Ni-NTA Fast Start Columns?
FAQ ID -836
表示
What to do if cell clumps are present after Buffer P2 addition when using LyseBlue Reagent?
FAQ ID -861
表示
Will the FastLane Cell cDNA Kit work with suspension cells?
FAQ ID -801
表示
What publicly funded Genome Sequencing Projects has QIAGEN's Sequencing Service been involved in?
FAQ ID -815
表示
What is the typical yield of site-specific labeled protein generated using the EasyXpress Site-Specific Biotin Kit?
FAQ ID -873
表示
What programs does your Sequencing Service use to ensure accurate base calling, Sequence Quality, and Alignment?
FAQ ID -831
表示
Where can I find a copy of the report file generated by running 'Maintenance Protocol I' on my BioRobot MDx?
FAQ ID -806
表示
Which QIAGEN plasmid preparation kits will contain LyseBlue Reagent?
FAQ ID -865
表示
Which fraction will contain soluble mitochondrial proteins using the Qproteome Cell Compartment Kit?
FAQ ID -839
表示
Which fraction will contain endosomal, microsomal and lysosomal proteins using the Qproteome Cell Compartment Kit?
FAQ ID -808
表示
Do I need to use RNase inhibitors with the RNeasy Kits?
FAQ ID -813
表示
Where can I find QIAGEN products for a specific gene or gene product?
FAQ ID -803
表示
Do the Buffers CE1 - CE4 of the Qproteome Cell Compartment Kit contain DTT or any reducing agent?
FAQ ID -824
表示
Can the FastLane Cell cDNA Kit also be used for qualitative end-point PCR?
FAQ ID -834
表示
Can the QuantiTect Primer Assays be used for detection of genomic DNA?
FAQ ID -811
表示
Can the FastLane Cell cDNA Kit be used with tissue?
FAQ ID -821
表示
Do you have a protocol for the isolation of bacteriophage P1 derived constructs with any of your plasmid kits?
FAQ ID -883
表示
Do you have an in vitro translation kit allowing the incorporation of seleno-methionine for X-Ray crystallography based protein analysis?
FAQ ID -879
表示
895 - Do you have a protocol for the isolation of endotoxin-free plasmid DNA using the QIAGEN Plasmid Midi Kit?
表示
Do you have a protocol for isolation of plasmid DNA using the Sigma Centrifuge 4?
-15
表示
Do you have a protocol for the isolation of BAC DNA using the QIAGEN Plasmid Midi Kit?
FAQ ID -881
表示
Can I reuse the Ni-NTA Agarose and Ni-NTA Superflow resins?
FAQ ID -802
表示
Can Buffer R1 of the R.E.A.L. Prep 96 Plasmid Kit be replaced with Buffer P1?
FAQ ID -823
表示
Are there specific recommendations for performing RT-PCR on RNA isolated from paraffin-embedded samples?
FAQ ID -828
表示
Can I stabilize adipose tissue using RNAprotect prior to RNA isolation?
FAQ ID -856
表示
Can I use the PhosphoProtein Purification Kit for the isolation of phosphorylated proteins from yeast?
FAQ ID -838
表示
Can I use QIAGEN's pQE vectors as templates in the EasyXpress Biotin Labeling Kits?
FAQ ID -874
表示
Can I use LyseBlue with R.E.A.L. Prep 96, QIAwell Ultra, or QIAprep 96 Turbo Miniprep Kits for the BioRobot systems?
FAQ ID -863
表示
Can I use my gene-specific primers with the FastLane Cell cDNA Kit and the QuantiTect Reverse Transcription Kit?
FAQ ID -812
表示
Have you tested the effect of inhibitors on PCR performance?
FAQ ID -818
表示
Do you sell the ATP-Dependent Exonuclease of the QIAGEN Large-Construct Kit separately?
FAQ ID -825
表示
How can I separate PCR fragments that are small and very close in size on an agarose gel?
FAQ ID -800
表示
Do you have information on in vivo RNA interference experiments?
FAQ ID -817
表示
I cannot see the LCD display fonts on the Sigma Centrifuge. How do I adjust the contrast?
FAQ ID -822
表示
I left Buffer P1 at room temperature after addition of RNase A, what shall I do?
FAQ ID -859
表示
How long does a typical in vitro translation reaction take with your large-scale EasyXpress protein synthesis kits?
FAQ ID -880
表示
How much protein can be produced with the EasyXpress Protein Synthesis Mega Kit?
FAQ ID -843
表示
Do you have a protocol for the isolation of very low-copy plasmids from Streptomyces spp.?
FAQ ID -893
表示
Do you have a protocol for the isolation of plasmid DNA from Citrobacter freundii?
FAQ ID -885
表示
Do you have a protocol for the isolation of plasmid DNA from Corynebacterium glutamicum?
FAQ ID -886
表示
Do you have a protocol for the isolation of plasmid DNA from Agrobacterium?
FAQ ID -898
表示
Do you have a protocol for the isolation of plasmid DNA from Borrelia spp.?
FAQ ID -884
表示
Do you have a protocol for the isolation of plasmid DNA from Bacillus subtilis?
FAQ ID -896
表示
Do you have a protocol for the isolation of plasmid DNA from yeast?
FAQ ID -853
表示
Do you have a protocol for the isolation of plasmid DNA from Lactobacillus spp.?
FAQ ID -887
表示
Do you have a protocol for the isolation of single-stranded DNA from M13 phage using QIAGEN Plasmid Kits?
FAQ ID -894
表示
Do you have a protocol for the isolation of plasmid DNA from Staphylococcus spp.?
FAQ ID -890
表示
Do you have a protocol for the isolation of plasmid DNA from Oligotropha carboxidovorans?
FAQ ID -888
表示
Do you have a protocol for the isolation of plasmid DNA from Proteus spp.?
FAQ ID -889
表示
What are the most commonly used protease inhibitors?
FAQ ID -53
表示
How should I quantify RNA isolated with RNeasy Kits?
FAQ ID -32
表示
Is plasmid DNA purified with QIAGEN Plasmid Purification Kits suitable for in vitro transcription?
FAQ ID -1
表示
How should I propagate pQE expression plasmids?
FAQ ID -58
表示
What are the compatibilities of different reagents with Ni-NTA matrices?
FAQ ID -49
表示
How is "Touchdown PCR" used to increase PCR specificity?
FAQ ID -75
表示
What should the starting template DNA quality and quantity be for PCR?
FAQ ID -74
表示
Why do I get smeared PCR products?
FAQ ID -87
表示
Why does my isolated RNA have a low OD 260/280 ratio?
FAQ ID -97
表示
When is chloramphenicol amplification of plasmids performed?
FAQ ID -3
表示
How can I remove imidazole from a protein sample?
FAQ ID -91
表示
How can I increase the amount of soluble recombinant protein in E. coli expression?
FAQ ID -64
表示
How can I avoid little or no RNA yields when using an RNeasy Kit?
FAQ ID -28
表示
What are the restriction sites of the pDrive Vector in the QIAGEN PCR Cloning Kit?
FAQ ID -160
表示
What are the molecular weights of proteins in the 6xHis Protein Ladder?
FAQ ID -169
表示
What are your recommendations for cotransfecting several plasmids?
FAQ ID -124
表示
What is the composition of Buffer EB?
FAQ ID -199
表示
Is mRNA isolation necessary for sensitive RT-PCR?
FAQ ID -111
表示
What are the recommended culture and buffer volumes for a very low-copy plasmid?
FAQ ID -168
表示
Should I use Ni-NTA Agarose in column or batch format for purification of 6xHis-tagged proteins?
FAQ ID -147
表示
What is the difference between disruption and homogenization in the RNeasy System?
FAQ ID -139
表示
Which Anti-His Antibody is the most sensitive for my protein of interest?
FAQ ID -172
表示
When should carrier be used with the QIAamp DNA Mini or the DNeasy Blood & Tissue Kit?
FAQ ID -100
表示
Why do I have to add beta-mercaptoethanol (beta-ME) to lysis Buffer RLT of the RNeasy Kits?
FAQ ID -101
表示
What is the recommended culture medium for the QIAprep System?
FAQ ID -154
表示
What is the RNase A concentration and composition of Buffer P1?
FAQ ID -198
表示
What is the genotype of the EZ Competent Cells?
FAQ ID -157
表示
What kind of PCR products can be cloned with the QIAGEN PCR Cloning Kit?
FAQ ID -165
表示
What is the principle behind Effectene Transfection Reagent?
FAQ ID -184
表示
What is the size of genomic DNA that is obtained with QIAGEN Genomic-tips?
FAQ ID -142
表示
How can I eliminate contaminating protein in my Ni-NTA 6xHis-tag protein purification?
FAQ ID -102
表示
How can I purify very small amounts of 6xHis-tagged protein using Ni-NTA technology?
FAQ ID -134
表示
How can I improve recoveries when using the QIAquick Kits?
FAQ ID -180
表示
How can I extract DNA from a polyacrylamide (PAGE) gel?
FAQ ID -120
表示
How can I improve ligation efficiency of DNA from a QIAEX II Gel Extraction Kit?
FAQ ID -141
表示
How can I isolate RNA from 1 gram of plant tissue?
FAQ ID -128
表示
How can I improve the performance of the HiSpeed QIAprecipitator module?
FAQ ID -144
表示
How can I improve transfection efficiency using Effectene Transfection Reagent?
FAQ ID -181
表示
What can I use to isolate RNA smaller than 200 nucleotides?
FAQ ID -115
表示
What epitopes do the Anti-His Conjugates and Anti-His Antibodies recognize?
FAQ ID -170
表示
What are the maximum culture volumes to use with the QIAGEN Plasmid Midi or Maxi Kit?
FAQ ID -167
表示
How should RNeasy Kits be stored and how long are they stable?
FAQ ID -103
表示
Is it possible to cleave the 6xHis-tag from an expressed protein?
FAQ ID -140
表示
How should I store plant material for DNA isolation using the DNeasy Plant Kit?
FAQ ID -114
表示
How should QIAGEN Plasmid Purification Kits be stored and for how long?
FAQ ID -192
表示
What are the features and benefits of the QIAexpress 6xHis Tag System?
FAQ ID -193
表示
What is the small band below my fragment of interest on an agarose gel after DNA cleanup using QIAquick?
FAQ ID -148
表示
Do you have transfection data for QIAGEN Transfection Reagents?
FAQ ID -158
表示
Do I need to use an RNase inhibitor in my RT reaction?
FAQ ID -119
表示
Do you have data showing effects of sample size on DNA yield and purity using the DNeasy 96 Blood & Tissue kit?
FAQ ID -129
表示
How can I avoid variable transfection efficiencies with SuperFect Reagent?
FAQ ID -179
表示
Does QIAGEN offer vectors for direct cloning of PCR products?
FAQ ID -146
表示
Can a QIAquick Gel Extraction Kit be used to obtain RNA from a formaldehyde gel?
FAQ ID -133
表示
Are QIAamp DNA isolation kits suitable for apoptosis studies?
FAQ ID -149
表示
Can DyeEx be used to clean up labeled DNA other than sequencing templates?
FAQ ID -137
表示
Are RNeasy spin columns sold separately?
FAQ ID -159
表示
Can I use QIAprep Miniprep kits for low-copy plasmids and cosmids?
FAQ ID -127
表示
Can I use the QIAquick PCR Purification Kit for restriction enzyme cleanup?
FAQ ID -130
表示
Can I use a QIAfilter Cartridge for purifying large plasmids?
FAQ ID -121
表示
Can I use Omniscript or Sensiscript RT's at a higher temperature?
FAQ ID -116
表示
How does imidazole affect my quantitation of protein?
FAQ ID -132
表示
How can I optimize the transfection of oligos and large plasmids using PolyFect Transfection Reagent?
FAQ ID -176
表示
How do you ensure that RNeasy buffers are RNase-free?
FAQ ID -113
表示
How can I purify DNA from soil, food and sewage samples for PCR?
FAQ ID -118
表示
How can I obtain DNA-free RNA using an RNeasy Midi or Maxi Kit?
FAQ ID -143
表示
How do I prepare an insert for pQE vectors?
FAQ ID -185
表示
How should I store Anti·His and Tag·100 Antibodies?
FAQ ID -194
表示
Do you have a protocol for purification of total DNA from insects?
FAQ ID -1254
表示
Is your Nuclease-Free Water fluorescence-free?
FAQ ID -1291
表示
Do you have a protocol for purification of total DNA from crude lysates?
FAQ ID -1255
表示
How should the GelPilot DNA Loading Dye be handled?
FAQ ID -1287
表示
What quality level does your Nuclease-Free Water have?
FAQ ID -1292
表示
What is the pH value of QIAGEN's Nuclease-Free Water?
FAQ ID -1290
表示
Does GelPilot DNA Loading Dye contain ethidium bromide?
FAQ ID -1286
表示
Are MaXtract tubes siliconized?
FAQ ID -1298
表示
Can phenol/chloroform be placed in the MaXtract tube for extraction at a later time?
FAQ ID -1299
表示
Should I input the dilution factor of my samples into the LiquiChip Analyser Software dilution factors of samples?
FAQ ID -1211
表示
What cell lines have been tested with the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1205
表示
What are the new features of the EasyXpress Insect Kit II compared to the original Protein Synthesis Insect kit?
FAQ ID -1220
表示
What are your recommendations for PCR template preparation for use with the EasyXpress Insect Kit II?
FAQ ID -1221
表示
Is it possible to increase nucleic acid concentrations when following protocols on the BioRobot EZ1?
FAQ ID -1232
表示
Is a saliva collection device provided in the RNeasy Protect Saliva Mini Kit?
FAQ ID -1213
表示
How should I prepare buffy coat samples for use on the BioRobot EZ1?
FAQ ID -1249
表示
Is it possible to use QIAGEN's pQE-Trisystem Vector with the EasyXpress Insect Kit II?
FAQ ID -1225
表示
Is training of lab personnel included with the purchase of a BioRobot EZ1?
FAQ ID -1239
表示
Where can I find information about the worktable setup on the BioRobot EZ1?
FAQ ID -1243
表示
Is RNAprotect Cell Reagent provided in the RNeasy Protect Cell Kit available separately?
FAQ ID -1217
表示
What vector do you recommend as template for in-vitro protein expression with the EasyXpress Insect Kit II?
FAQ ID -1224
表示
What type of promoter should my template have for in-vitro protein expression with the EasyXpress Insect Kit II?
FAQ ID -1223
表示
What is the difference between various FlexiTube siRNAs listed for the same target gene, and which one should I choose?
FAQ ID -1206
表示
Will the Qproteome Plasma Membrane Protein Kit work with starting materials other than adherent mammalian cells?
FAQ ID -1202
表示
What disposables are required for nucleic acid isolations on the BioRobot EZ1?
FAQ ID -1246
表示
What is the protein yield when using the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1201
表示
What is the maximum number of cells that can be used with the AllPrep RNA/Protein Kit ?
FAQ ID -1208
表示
Do the foils sealing the EZ1 Reagent Cartridges have to be manually removed prior to loading the robot?
FAQ ID -1240
表示
What is the smallest and the largest protein that you tested for expression with the EasyXpress Insect Kit II?
FAQ ID -1218
表示
What is the size of the BioRobot EZ1?
FAQ ID -1245
表示
Does anything have to be added to express post-translational modifications (PTMs) with the EasyXpress Insect Kit II?
FAQ ID -1226
表示
Do you have a protocol for isolating cytoplasmic RNA from animal cells using the RNeasy Mini Kit?
FAQ ID -1207
表示
Do you have a protocol for purification of miRNA from animal cells using the RNeasy Plus Mini Kit and RNeasy MinElute Cleanup Kit?
FAQ ID -1258
表示
Do you have a protocol for purification of cytoplasmic RNA from animal cells?
FAQ ID -1257
表示
Can cells stabilized with RNAprotect Cell Reagent be used for cell sorting by flow cytometry (FACS)?
FAQ ID -1216
表示
Can glycosylated proteins be expressed using the EasyXpress Insect Kit II?
FAQ ID -1227
表示
Can the Strep-Tactin Magnetic Beads of the Qproteome Plasma Membrane Protein Kit be reused?
FAQ ID -1204
表示
Can RNAprotect Saliva Reagent be purchased separately?
FAQ ID -1214
表示
Can you recommend a Reagent or Kit for stabilizing RNA in cultured cells?
FAQ ID -1215
表示
Can the RLT lysate of the BioSprint DNA Plant protocol be stored frozen?
FAQ ID -1248
表示
Can the Qproteome Plasma Membrane Protein Kit be used with tissue samples?
FAQ ID -1200
表示
How can we get our BioRobot EZ1 upgraded when new protocols are launched?
FAQ ID -1241
表示
How can I decontaminate the BioRobot EZ1?
FAQ ID -1231
表示
How much active protein can be expressed in-vitro using the EasyXpress Insect Kit II, and how much time does it take?
FAQ ID -1222
表示
How do you ensure that concentrated RNA is purified from saliva using the RNeasy Protect Saliva Mini Kit?
FAQ ID -1212
表示
Do you have a protocol for purification of total DNA from yeast?
FAQ ID -1253
表示
How many freeze-thaw cycles can the various reaction mixes in the EasyXpress Insect Kit II tolerate?
FAQ ID -1219
表示
Do you have a protocol for the isolation of DNA from buccal cells using the BioRobot EZ1?
FAQ ID -1260
表示
Do you have a protocol for transfection of suspension cell lines (Jurkat and K562) with siRNA?
FAQ ID -1250
表示
How are plasma membrane containing vesicles eluted off the ligand in the Qproteome Plasma Membrane Protein procedure?
FAQ ID -1203
表示
Do you have a protocol for transfection of differentiated macrophage cell lines (THP) with siRNA?
-1
表示
Do you have a protocol for transfection of macrophage cell lines (J774.A1 and RAW 264.7) with siRNA?
FAQ ID -1251
表示
Can I use a centrifuge instead of vacuum when using the QIAquick 96 PCR Purification Kit?
FAQ ID -293
表示
If I want to use BioMag particles, do I have to buy a QIAGEN magnet too or can I use one that I already have?
FAQ ID -266
表示
Can the PAXgene Blood RNA Tubes undergo freeze/thaw cycles?
FAQ ID -2471
表示
Should I use Omniscript or Sensiscript for reverse transcription of low-copy mRNA?
FAQ ID -297
表示
I used to buy BioMag particles from a company by another name? Are your BioMag particles the same thing?
FAQ ID -263
表示
What are the main differences between other magnetic beads and the BioMag particles?
FAQ ID -272
表示
My BioMag is about to expire, is it still any good?
FAQ ID -268
表示
If I am using BioMag Streptavidin to capture biotinylated oligos, how can I then remove the oligos?
FAQ ID -279
表示
How magnetically responsive is BioMag?
FAQ ID -265
表示
What is the recipe for LB?
FAQ ID -212
表示
What is the maximum binding capacity of RNeasy spin columns?
FAQ ID -290
表示
What is the recipe for 2x YT?
FAQ ID -213
表示
Why does my DNA sample float out of the slot when loading it onto an agarose gel?
FAQ ID -205
表示
Why is an ice-incubation step included during reaction set-up when following the QuantiTect RT-PCR but not the QuantiTect PCR protocol.
FAQ ID -283
表示
What sequencing primers can I use with the pDrive cloning vector of the QIAGEN PCR Cloning Kit?
FAQ ID -292
表示
What is the composition of Buffer P2?
FAQ ID -203
表示
What is the difference between the QIAamp MinElute Virus Spin and the MinElute Virus Vacuum Kit?
FAQ ID -295
表示
What is the composition of the QIAGEN Multiplex PCR Buffer?
FAQ ID -289
表示
What is the difference between the Fc specific versions of your secondary antibody BioMag particles and the non-specific?
FAQ ID -275
表示
Can I use HEPES buffer instead of phosphate in my Ni-NTA column?
FAQ ID -291
表示
Can I use my own cycling conditions with the QIAGEN Multiplex PCR Kit?
FAQ ID -287
表示
Can I select FITC labeled cells with BioMag?
FAQ ID -278
表示
A white precipitate has formed in my 10x RT buffer. Is it still ok to use?
FAQ ID -216
表示
Can I use BioMag particles with any specific primary antibody?
FAQ ID -273
表示
Can I clean up my DNase treated RNA samples using RNeasy columns?
FAQ ID -286
表示
Are BioMag particles stable in other solvents?
FAQ ID -267
表示
Can BioMag be used for positive and negative selection?
FAQ ID -269
表示
How can I avoid poor immunolocalization morphology with Anti-His Antibodies?
FAQ ID -200
表示
For how long are BioMag Particles stable?
FAQ ID -262
表示
How can I prevent non-specific binding when using BioMag?
FAQ ID -277
表示
How do I prevent bubbles from forming in my Ni-NTA agarose column?
FAQ ID -285
表示
How can I purify mRNA from total RNA using an Oligotex Direct mRNA Kit?
FAQ ID -201
表示
How can one determine the optimal annealing temperature for a specific PCR assay?
FAQ ID -288
表示
Does QIAGEN sell Q-Solution separately?
FAQ ID -204
表示
What is the composition of Protein Precipitation Solution?
FAQ ID -2810
表示
What is the composition and concentration of Glycogen Solution in Gentra Puregene Kits?
FAQ ID -2812
表示
What is the composition of Buffer RDD?
FAQ ID -2800
表示
What is the composition of Cell Lysis Solution?
FAQ ID -2809
表示
What is the composition of DNA Hydration Solution in Gentra Puregene Kits?
FAQ ID -2813
表示
What is the composition of Cell Suspension Solution?
FAQ ID -2811
表示
Which heating block is recommended for the pyrosequencing annealing step?
FAQ ID -2838
表示
What is the recommended amplicon size for CpG assays?
FAQ ID -2825
表示
Which end of the PCR primer for pyrosequencing should be biotinylated?
FAQ ID -2839
表示
Which competent E. coli cells should I use to amplify the SureSilencing shRNA Plasmids?
FAQ ID -2890
表示
Which analyses can be performed with the PyroMark Q96 ID software version 1.0?
FAQ ID -2845
表示
Which kits can be used in combination with the PyroMark CpG Assays and PyroMark Custom Assays?
FAQ ID -2822
表示
What region of LINE gets targeted by the assay for PyroMark Q96 MD or PyroMark Q24?
-1
表示
What should be the single peak height for the PyroMark Control Oligo on the different PyroMark instruments?
FAQ ID -2852
表示
Does the same U1 promoter in the SureSilencing shRNA Plasmids express shRNA in human, mouse, and rat cell lines?
FAQ ID -2887
表示
What is the amplicon length of the PyroMark CpG LINE assay?
-1
表示
How are the PyroMark CpG Assays reconstituted?
FAQ ID -2817
表示
How can I use the SureSilencing shRNA Plasmids for stable transfection and knock down in a cell line that is already resistant to both neomycin and puromycin?
FAQ ID -2895
表示
Does the PyroMark LINE assay target all LINE sequences?
-1
表示
Can I use fluorescence microscopy to assess the transfection efficiency of the SureSilencing shRNA Plasmids with GFP in my model cell line of interest?
FAQ ID -2894
表示
Can I use my own siRNA design?
FAQ ID -2897
表示
Can I reclone the insert sequences from the SureSilencing shRNA Plasmids into a viral-based vector?
FAQ ID -2896
表示
Can I directly transfect SureSilencing shRNA Plasmids into my cells?
FAQ ID -2899
表示
Can I order the nucleotides from PyroMark Gold Reagents separately?
FAQ ID -2827
表示
Do any of the SureSilencing shRNA Plasmids contain inducible promoters?
FAQ ID -2888
表示
Does QIAGEN offer a design of Custom PyroMark CpG Assays?
FAQ ID -2818
表示
Can unused wells in a pyrosequencing plate be used in the next run?
FAQ ID -2872
表示
Can PyroMark Gold reagents be vortexed?
FAQ ID -2844
表示
Can the PyroMark Q96 CpG LINE assay be used with an ID system?
-1
表示
What are the features of PyroMark CpG Assays e.g. in terms of design, validation?
FAQ ID -2821
表示
How do I reduce background peaks in the pyrosequencing pyrogram?
FAQ ID -2877
表示
What are the features of the new PyroMark Q96 ID software 2.5?
FAQ ID -2867
表示
What are the changes of PyroMark Assay Design Software Version 2.0 compared to 1.0?
FAQ ID -2849
表示
Is there a user manual available for the PyroMark Assay design software?
FAQ ID -2851
表示
Should I use the SureSilencing shRNA Plasmids with the neomycin-resistance marker, the puromycin-resistance marker, or the GFP reporter gene?
FAQ ID -2882
表示
What else do I need to complete an experiment using the SureSilencing shRNA Plasmids?
FAQ ID -2889
表示
What cell line does QIAGEN use for quality control testing of the SureSilencing shRNA Plasmids?
FAQ ID -2885
表示
What is included in a PyroMark Custom Assay?
FAQ ID -2815
表示
What cell lines can I use with the SureSilencing shRNA Plasmids?
FAQ ID -2891
表示
How many nucleotides of a homopolymer can be resolved in pyrosequencing?
FAQ ID -2871
表示
What concentration should be used for the sequencing primer in pyrosequencing?
FAQ ID -2826
表示
How many CpG sites are analyzed by the PyroMark CpG LINE assay?
-1
表示
How do I set up a PyroMark CpG Assay?
FAQ ID -2814
表示
How long should I wait after transfection before enriching my transfected cells, validating knock down, and looking for phenotypic changes?
FAQ ID -2893
表示
How many times can the cartridges for Pyromark Q24 or PyroMark Q96 ID instruments are reused?
FAQ ID -2863
表示
Is the CpG software included in the PyroMark instruments to study methylation status?
FAQ ID -2842
表示
Is the expression level of miRNA precursors lower compared to that of mature miRNAs?
FAQ ID -2807
表示
In which format can PyroMark CpG Assays be ordered?
FAQ ID -2824
表示
How many times can the CDTs, NDTs, and RDTs be used?
FAQ ID -2865
表示
How many times can vacuum troughs be re-used with the PyroMark Vacuum Preparation Stations?
FAQ ID -2848
表示
What is the meaning of the abbreviations NDT and CDT and what are the differences?
FAQ ID -2841
表示
What is the PyroMark Q96 Data Converter?
FAQ ID -2868
表示
What is the composition of RBC Lysis Solution?
FAQ ID -2808
表示
What is the concentration of PyroMark Control Oligo?
FAQ ID -2846
表示
What is the pyrosequencing data exchange tool for?
FAQ ID -2864
表示
What is the reason for signals ceasing in the middle of a pyrosequencing run?
FAQ ID -2875
表示
What is the reason for split peaks appearing in between dispensations on my pyrosequencing pyrogram?
FAQ ID -2881
表示
What is the reason for a high substrate peak in the pyrosequencing pyrogram?
FAQ ID -2879
表示
What is the composition of Buffer FRN?
FAQ ID -2802
表示
What is the composition of Buffer PKD?
FAQ ID -2801
表示
What is the composition of Buffer APP?
FAQ ID -2804
表示
What is the composition of Buffer ALO?
FAQ ID -2805
表示
What is the composition of Buffer APL?
FAQ ID -2803
表示
Which analyses can be performed with the PyroMark Q96 MD software?
FAQ ID -2866
表示
Will dUTP in a PCR reaction affect pyrosequencing?
FAQ ID -2843
表示
Will the primer sequence for the PyroMark CpG Assay be provided?
FAQ ID -2823
表示
What is the use of the PyroMark Q24 Validation Oligo?
FAQ ID -2855
表示
Which purity grade is recommended for pyrosequencing primers?
FAQ ID -2832
表示
Which PyroMark Gold Q96 Reagent should be used for which instrument and application?
FAQ ID -2836
表示
What kind of shaker should be used for the pyrosequencing binding step?
FAQ ID -2837
表示
What is the sensitivity limitation for pyrosequencing?
FAQ ID -2840
表示
What is the SureSilencing shRNA Plasmids guarantee?
FAQ ID -2898
表示
What primers may I use to sequence the shRNA cassette within the SureSilencing shRNA Plasmids?
FAQ ID -2886
表示
Where can I order the Streptavidin Sepharose beads for pyrosequencing?
FAQ ID -2850
表示
Where to find explanations to the warning given by the PyroMark software after run data analysis?
FAQ ID -2874
表示
Does the Pyromark Assay Design or application software give any cycling conditions for individual assay primers or a PCR setup pipetting scheme?
FAQ ID -2862
表示
Does the PyroMark CpG LINE assay target mouse transposons as well?
-1
表示
How are the PyroMark CpG Assays shipped and stored?
FAQ ID -2816
表示
How do I find the SureSilencing shRNA Plasmids for my gene of interest?
FAQ ID -2883
表示
How do I prevent a drifting baseline in my pyrosequencing pyrogram?
FAQ ID -2878
表示
How are the SureSilencing shRNA Plasmids shipped?
FAQ ID -2884
表示
Is the pH indicated in the formulation sheet for Screening Suite buffers the final pH?
FAQ ID -1123
表示
Is the surface tension of the crystallization supports of the EasyXtal 15-Well Tools similar to that of a siliconized cover slide?
FAQ ID -1107
表示
Do you have a protocol for high-throughput purification of plasmid DNA using the BioRobot Universal System?
FAQ ID -1191
表示
Is it possible to collect intact mitochondria before or after the density gradient centrifugation step of the Qproteome Mitochondria Isolation protocol?
FAQ ID -1187
表示
What are the applications the EasyXtal 15-Well Tool can be used for?
FAQ ID -1111
表示
Is the EasyXtal Tool compatible with liquid-handling systems and visualization robots?
FAQ ID -1118
表示
What EZ1 DNA Investigator protocol is recommended for very precious samples?
FAQ ID -1154
表示
What cell lines have been tested with the Fastlane Cell cDNA Kit?
FAQ ID -1175
表示
What does transcript variant mean when searching for specific QuantiTect Primer Assays?
FAQ ID -1137
表示
What does 'QIAGEN Certified Solution' for Protein Crystallization mean?
FAQ ID -1121
表示
How many protein crystallization conditions are available at QIAGEN?
FAQ ID -1119
表示
How much detection reagent do you generally recommend for LiquiChip Assays?
FAQ ID -1159
表示
How many LiquiChip beads are recommended for an xMAP experiment?
FAQ ID -1161
表示
How many cells can be used with the Qproteome Mitochondria Isolation Kit, and how much mitochondrial protein can be expected?
FAQ ID -1189
表示
How many drops can be set up on a protein crystallization support?
FAQ ID -1110
表示
How much solution can I add to an EasyXtal 15-Well Tool reservoir well?
FAQ ID -1114
表示
If I cannot find a QuantiTect Primer Assay for my target gene in rat, can I use the assays for the orthologous genes in mouse and human?
FAQ ID -1145
表示
In which formats are crystallization condition Screening Suites available?
FAQ ID -1127
表示
If a QuantiTect Primer Assay has more than one version number, does this mean that earlier assay versions may not work?
FAQ ID -1136
表示
How sensitive is the LiquiChip Reader?
FAQ ID -1157
表示
What is a QuantiTect Primer Assay?
FAQ ID -1141
表示
How much time is needed for a LiquiChip assay point measurement?
FAQ ID -1162
表示
What is the delivery time for QuantiTect Primer Assays?
FAQ ID -1142
表示
What kind of strategy for initial screening of protein crystallization conditions do you recommend?
FAQ ID -1120
表示
Why are there various different QuantiTect Primer Assays for my gene (previous versions, transcript variants)?
FAQ ID -1133
表示
When should the EZ1 DNA Investigator Normalization protocol be used?
FAQ ID -1155
表示
Where can I find the composition tables for solutions used in individual Crystallization Screening Suites?
FAQ ID -1124
表示
When searching for a QuantiTect Primer Assay for my gene of interest, why do I only find the assay for human but not for rat?
FAQ ID -1139
表示
Can the EZ1 DNA Investigator Tip Dance protocol cope with any solid matrix remaining in the sample tube?
FAQ ID -1153
表示
What type of magnet do you recommend for handling the magnetic beads in the Qproteome Plasma Membrane Protein protocol?
FAQ ID -1193
表示
What starting material can be used with the Qproteome Mitochondria Isolation Kit?
FAQ ID -1184
表示
Are EasyXtal 15-Well Tools stackable?
FAQ ID -1116
表示
Which QuantiTect Primer Assay should I choose for my gene of interest?
FAQ ID -1135
表示
Why can I not find the QuantiTect Primer Assay in GeneGlobe that I had previously ordered from QIAGEN?
FAQ ID -1138
表示
Which chemical products do you use to prepare screening solutions for protein crystallization?
FAQ ID -1122
表示
Will proteins eluted in the Qproteome Plasma Membrane Protein protocol be modified, e.g. with the ligand?
FAQ ID -1195
表示
Why does the QuantiTect Primer Assay for my gene of interest have only one version number?
FAQ ID -1134
表示
Will the ligand in the Qproteome Plasma Membrane Protein protocol be specific for plasma membrane exclusively?
FAQ ID -1198
表示
Will integral, peripheral as well as lipid-anchored plasma membrane proteins be isolated with the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1199
表示
Why is there no QuantiTect Primer Assay for my gene of interest?
FAQ ID -1140
表示
What is the dynamic range of detection of the LiquiChip Reader?
FAQ ID -1158
表示
What is the EasyXtal 15-Well Tool made of?
FAQ ID -1106
表示
Can the nuclei and cell debris fraction generated in the QProteome Mitochondria isolation procedure be used for further fractionation?
FAQ ID -1185
表示
Can the EZ1 DNA Forensic Card be used with the EZ1 DNA Investigator Kit?
FAQ ID -1151
表示
Can the EasyXtal 15-Well Tools be reused?
FAQ ID -1117
表示
Can the Qproteome Plasma Membrane Protein Kit be used with suspension cells?
FAQ ID -1194
表示
Can your Tag antibody recognize rat MAPK1 also?
-100
表示
Can the remaining fractions obtained in the Qproteome Plasma Membrane Protein procedure be used in downstream assays?
FAQ ID -1197
表示
Can xMAP kits from other Luminex partners be used on the LiquiChip System purchased from QIAGEN?
FAQ ID -1156
表示
Can the Spin Columns of the Qproteome Albumin/IgG Depletion Kit be reused?
FAQ ID -1173
表示
Are protein modifications such as glycosylation problematic when using the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1196
表示
Are scoring sheets available for each crystallization condition Screening Suite?
FAQ ID -1125
表示
Can mitochondria separated with the Qproteome Mitochondria Isolation Kit be used for downstream DNA isolation?
FAQ ID -1188
表示
Can acetone be used for precipitation of protein from Buffer RLT lysates generated with RNeasy Kits?
FAQ ID -1164
表示
Can I increase the annealing temperature recommended for QuantiTect Primer Assays used with the QuantiTect SYBR Green PCR Kits?
FAQ ID -1146
表示
Does the EasyXtal Tool conform to an SBS format?
FAQ ID -1115
表示
How are NeXtal deep-well blocks sealed? Can they be resealed?
FAQ ID -1128
表示
Do you have WGA protocols for starting materials not mentioned in the REPLI-g Handbooks?
FAQ ID -1160
表示
Do you have a protocol for the isolation of genomic DNA from whole blood for use in MRC-Holland MLPA® assays?
FAQ ID -1169
表示
Do you have a protocol for the purification of 6xHis-tagged proteins using BioSprint?
FAQ ID -1167
表示
How easy is it to scoop up a protein crystal with the lip around the crystallization supports of the EasyXtal 15-Well Tools?
FAQ ID -1113
表示
How is the quality of the crystallization condition Screening Suites guaranteed?
FAQ ID -1126
表示
How do I use EasyXtal Crystallization Tools?
FAQ ID -1105
表示
How did you determine that your AllStar Negative Control siRNA binds to RISC?
FAQ ID -1180
表示
How does the sealing efficiency of the crystallization supports of the EasyXtal 15-Well Tool compare to grease?
FAQ ID -1109
表示
Do you have a kit for protein isolation from mitochondria prepared with your Qproteome Mitochondria Isolation Kit?
FAQ ID -1190
表示
Do you have a kit for the isolation of RNA from formalin-fixed, paraffin-embedded samples?
FAQ ID -1174
表示
Do QuantiTect Primer Assays contain SYBR Green dye?
FAQ ID -1143
表示
Do I need an ultracentrifuge for the density gradient centrifugation step in the Qproteome Mitochondria Isolation protocol?
FAQ ID -1186
表示
Do protein crystals stick to the walls of cavities when using the DropGuard crystallization supports?
FAQ ID -1108
表示
Do you have a protocol for evaluating pipetting accuracy of the BioRobot EZ1?
FAQ ID -1131
表示
Do you have a protocol for purification of DNA from stool samples for pathogen detection using BioSprint Instruments?
FAQ ID -1165
表示
Do you have a protocol for purification of DNA from stool samples using BioSprint Instruments?
FAQ ID -1166
表示
Do you have a protocol for evaluating temperature accuracy of the BioRobot EZ1?
FAQ ID -1168
表示
How can I analyze proteins from exosomes and other extracellular vesicles (EVs) obtained with the exoEasy Maxi Kit by SDS-PAGE?
FAQ ID - 3707
表示
What is the concentration of SureENTRY Transduction Reagent?
FAQ ID - 3708
表示
Is it possible to modify the transduction protocol for Cignal Lenti Reporter Assays to save some pipetting steps?
FAQ ID - 3709
表示
Is it possible to get a Custom RT2 Profiler PCR Array, cat. # 330131, with primer assays targeting transcripts of different species, e.g. assays targeting transcripts from mouse and assays targeting transcripts from human, on one plate?
FAQ ID - 3710
表示
Can I store the QIAseq Beads of the QIAseq Targeted DNA Panel at -20°C?
FAQ ID - 3711
表示
Is it possible to purchase Buffer VXL which is part of the QIAamp cador Pathogen Mini Kit, (Cat No.: 54104, 54106) separately?
FAQ ID - 3712
表示
What sample tubes can I use on my QIAsymphony SP system?
FAQ ID - 3713
表示
How can I decontaminate my QIAsymphony SP / AS system?
FAQ ID - 3714
表示
What is the difference between the QIAamp UCP DNA Micro Kit (cat. no. 56204) and RNeasy UCP Kits (cat. no. 73934) and non-UCP QIAGEN purification kits?
FAQ ID - 3715
表示
Can I use carrier RNA with the RNeasy UCP Micro Kit (cat. no. 73934)?
FAQ ID - 3716
表示
Can other QIAGEN buffers from non-UCP kits (e.g. AW1 instead of AUW1) be used with the QIAamp UCP DNA Micro Kit (cat. no. 56204)?
FAQ ID - 3717
表示
How is the Pyromark Q48 cartridge to be cleaned?
FAQ ID - 3718
表示
Can the disc and absorber strips for the Pyromark Q48 be reused?
FAQ ID - 3720
表示
What is the dead volume of the cartridges in PyroMark Q48?
FAQ ID - 3719
表示
How much DNA is needed in the PyroMark Q48?
FAQ ID - 3721
表示
Can I transfer my assays from PyroMark Q24/Q96 to PyroMark Q48 Autoprep?
FAQ ID - 3723
表示
Can I use PyroMark Q48 for diagnostics?
FAQ ID - 3722
表示
Can I analyze my Next Generation Sequencing (NGS) samples on the QIAxcel for Quality control?
FAQ ID - 3724
表示
How long does an Investigator Quantiplex Pro run take?
FAQ ID - 3727
表示
Can I buy the 1 ml Bead Plates from the DNeasy UltraClean 96 Microbial Kit (384) separately?
FAQ ID - 3726
表示
Is an additional proteinase K digest possible with DNeasy PowerSoil Kit and DNeasy PowerLyzer Kit?
FAQ ID - 3725
表示
On which real-time cyclers is the Investigator Quantiplex Pro Kit validated?
FAQ ID - 3728
表示
Can the Investigator Quantiplex Pro Kit be run on on the Rotor-Gene Q?
FAQ ID - 3729
表示
Which real-time cycler software version can be used to run the Investigator Quantiplex Pro Kit?
FAQ ID - 3730
表示
Do I have to calibrate new dyes on my Applied Biosystems 7500 or 7500 Fast Real-Time PCR System?
FAQ ID - 3732
表示
How long can I store the dilutions of the Male Control DNA M1 standards at 8°C?
FAQ ID - 3733
表示
What do I have to consider if I am using the Applied Biosystems SDS software version 1.2.3 in order to run an Investigator Quantiplex Pro reaction?
FAQ ID - 3731
表示
Why do I observe a CT shift for the internal control in some samples in comparison to the CT value for the internal control of the dilution series of the Male Control DNA M1?
FAQ ID - 3734
表示
Which human target is used for the quantification?
FAQ ID - 3736
表示
How long are the target sequences of Investigator Quantiplex Pro?
FAQ ID - 3735
表示
At what temperature should I store the Investigator Quantiplex Pro Kit?
FAQ ID - 3737
表示
How can I streamline the quantification workflow?
FAQ ID - 3738
表示
Does QIAGEN offer an anti-GFP gapmer control?
FAQ ID - 3739
表示
How long does an Investigator Quantiplex Pro RGQ run take?
FAQ ID - 3740
表示
On which real-time cyclers is the Investigator Quantiplex PRO RGQ Kit validated?
FAQ ID - 3741
表示
Which Rotor-Gene Q System can be used to run the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3742
表示
Which real-time cycler software version can be used to run the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3743
表示
How long can I store the dilutions of the Male Control DNA M1 standards at 2–8°C?
FAQ ID - 3744
表示
How long are the target sequences of the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3746
表示
Why do I observe a CT shift for the Internal Control in some samples in comparison to the CT value for the Internal Control of the dilution series of the Male Control DNA M1?
FAQ ID - 3745
表示
Which human target is used for the quantification?
FAQ ID - 3747
表示
At what temperature should I store the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3748
表示
How can I streamline the quantification workflow?
FAQ ID - 3749
表示
Which fixation method is used in the PAXgene Tissue System?
FAQ ID - 3600
表示
What is the fixation reagent of PAXgene Tissue FIX?
FAQ ID - 3601
表示
What is the stabilization reagent of PAXgene Tissue STABILIZER?
FAQ ID - 3602
表示
What is the maximum tissue size that can be fixed in a PAXgene Tissue FIX Container (50 ml)?
FAQ ID - 3604
表示
Why are two reagents used in the PAXgene Tissue System?
FAQ ID - 3603
表示
Which conditions are recommended for the storage of tissues in PAXgene Tissue STABILIZER?
FAQ ID - 3605
表示
Is it possible to process formalin-fixed and PAXgene Tissue fixed samples together in one run?
FAQ ID - 3606
表示
Is it necessary to clean a processor normally used for formalin-fixed tissue before using it with PAXgene Tissue fixed tissue?
FAQ ID - 3607
表示
Is it possible to integrate the PAXgene Tissue STABILIZER into tissue processing?
FAQ ID - 3608
表示
Are immunohistochemistry (IHC) assays developed for formalin-fixed, paraffin-embedded (FFPE) tissues compatible with PAXgene Tissue fixed, paraffin-embedded (PFPE) tissues?
FAQ ID - 3609
表示
Is it possible to use formalin-fixed, paraffin-embedded (FFPE) kits and protocols to isolate biomolecules from PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3610
表示
How well is RNA integrity preserved in PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3611
表示
How well is DNA integrity preserved in PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3612
表示
Are special kits and protocols required to isolate biomolecules from PAXgene Tissue fixed, cryo-embedded (PFCE) tissue?
FAQ ID - 3614
表示
What are the yield and integrity of nucleic acids isolated from blocks of PAXgene Tissue fixed, cryo-embedded (PFCE) tissue?
FAQ ID - 3613
表示
Does the PAXgene Tissue RNA Kit co-purify small RNAs?
FAQ ID - 3615
表示
Which kits and protocols can be used to isolate nucleic acids from microdissected PAXgene Tissue fixed, paraffin-embedded (PFPE) and PAXgene Tissue fixed, cryo-embedded (PFCE) specimens?
FAQ ID - 3617
表示
Can proteins be extracted from PAXgene Tissue fixed specimens?
FAQ ID - 3616
表示
What is the PCR performance of DNA purified from PAXgene Tissue fixed, paraffin-embedded (PFPE) and PAXgene Tissue fixed, cryo-embedded (PFCE) tissue compared to DNA from snap frozen or formalin-fixed, paraffin-embedded (FFPE) tissue?
FAQ ID - 3618
表示
How is the quality of proteins purified from PAXgene Tissue fixed and stabilized tissue?
FAQ ID - 3619
表示
How do I prepare Buffer MP?
FAQ ID - 3620
表示
We recently changed the OS from Windows XP to Windows 7. When re-installing software Pyromark Q24 2.0.6, it fails to analyse the results. Any suggestions?
FAQ ID - 3621
表示
Can the RNeasy kits be used to extract RNA from saliva collected using the Oragene collection kit?
FAQ ID - 3623
表示
How do I analyze codon 61 mutations with the RAS extension kit (cat. no. 971590)?
FAQ ID - 3622
表示
Are the QIAshredder columns included in various QIAGEN kits the same?
FAQ ID - 3624
表示
Do I need to use a blood collection set with the PAXgene Blood ccfDNA Tube?
FAQ ID - 3626
表示
Are QR codes recognized by QIAsymphony?
FAQ ID - 3625
表示
Does the insert sequence provided in the specification sheet correspond to the target sequence or to anti-sense sequence?
FAQ ID - 3627
表示
What is the reagent in the PAXgene Blood ccfDNA Tube?
FAQ ID - 3632
表示
What is the shelf life of unused PAXgene Blood ccfDNA Tubes?
FAQ ID - 3633
表示
How should unused PAXgene Blood ccfDNA Tubes be stored?
FAQ ID - 3634
表示
Are PAXgene Blood ccfDNA Tubes sterile?
FAQ ID - 3636
表示
Are there special considerations for phlebotomy when using the PAXgene Blood ccfDNA Tube (blood collection set, discard tube, positioning of the tube, issues with short draws, etc.)?
FAQ ID - 3635
表示
What is the expected ccfDNA yield from plasma generated from 10 ml of blood?
FAQ ID - 3637
表示
How long can whole blood stabilized in PAXgene Blood ccfDNA Tubes be stored at room temperature?
FAQ ID - 3639
表示
Can I use plasma from underfilled PAXgene Blood ccfDNA Tubes?
FAQ ID - 3638
表示
Can whole blood in PAXgene Blood ccfDNA Tubes be stored at temperatures below 15°C?
FAQ ID - 3641
表示
Can whole blood in PAXgene Blood ccfDNA Tubes be stored at temperatures above 25°C?
FAQ ID - 3640
表示
Can whole blood be frozen in PAXgene Blood ccfDNA Tubes?
FAQ ID - 3642
表示
How long and at which temperature can plasma generated from whole blood in PAXgene Blood ccfDNA Tubes be stored?
FAQ ID - 3644
表示
Is double centrifugation required for plasma processing?
FAQ ID - 3643
表示
How should I thaw frozen plasma samples?
FAQ ID - 3645
表示
What should I do if cryoprecipitates form while thawing a frozen plasma sample?
FAQ ID - 3646
表示
How many extractions can I perform with a QIAsymphony PAXgene Blood ccfDNA Kit, using the 2.4 ml or the 4.8 ml protocols?
FAQ ID - 3649
表示
Which plasma volumes can I process with the QIAsymphony PAXgene Blood ccfDNA protocols?
FAQ ID - 3648
表示
How long after first use can a reagent cartridge be stored for further use?
FAQ ID - 3650
表示
For what type of sample material is the QIAsymphony PAXgene Blood ccfDNA Kit intended?
FAQ ID - 3652
表示
Which tubes are recommended for the QIAsymphony sample rack
FAQ ID - 3653
表示
Which protocol line should I use to process plasma samples?
FAQ ID - 3654
表示
How should eluates produced with the PAXgene Blood ccfDNA System be stored?
FAQ ID - 3657
表示
Does the QIAsymphony PAXgene Blood ccfDNA Kit also allow eluting ccfDNA in less than 60 µl?
FAQ ID - 3656
表示
Which downstream applications have been tested with ccfDNA purified from whole blood collected and processed with the PAXgene Blood ccfDNA System?
FAQ ID - 3658
表示
What is the shelf life of the QIAsymphony PAXgene Blood ccfDNA Kit?
FAQ ID - 3651
表示
Which elution volumes are available with the QIAsymphony PAXgene Blood ccfDNA Kit?
FAQ ID - 3655
表示
Why is a blood collection set required to collect blood into the PAXgene Blood ccfDNA Tube?
FAQ ID - 3628
表示
Can I use a different brand blood collection set with the PAXgene Blood ccfDNA Tube?
FAQ ID - 3630
表示
Can reagent from the PAXgene Blood ccfDNA Tube flow back into the patient’s arm?
FAQ ID - 3629
表示
What is the blood draw volume of the PAXgene Blood ccfDNA Tube
FAQ ID - 3631
表示
Where can I find the gene list for a specific RT² Profiler PCR Array?
FAQ ID - 3684
表示
Is it possible to store nucleic acids extracted using the SpeedXtract Virus Kit?
FAQ ID - 3680
表示
Can REPLI-g WGA be used to amplify cDNA if the cDNA is dsDNA (double-stranded DNA)?
FAQ ID - 3686
表示
What is the difference between RT² Profiler PCR Array and RT² Profiler PCR Array PLUS version?
FAQ ID - 3685
表示
I would like to stop during the library preparation procedure. When can I do that?
FAQ ID - 3687
表示
Should total RNA or small enriched RNA be used as the starting material for the QIAseq miRNA Library Kit?
FAQ ID - 3659
表示
Total RNA from what sample types are compatible with the QIAseq miRNA Library Kit?
FAQ ID - 3660
表示
Can miRNA sequencing libraries be prepared from total RNA isolated from heparinized plasma samples?
FAQ ID - 3661
表示
Are any components of the QIAseq miRNA Library Kit interchangeable with components from other QIAGEN kits?
FAQ ID - 3662
表示
What are recommended stopping points during the QIAseq miRNA Library Kit procedure?
FAQ ID - 3663
表示
When multiplexing samples, what sample indexes should be combined?
FAQ ID - 3664
表示
What is the maximum number of available sample indexes?
FAQ ID - 3665
表示
Can I still perform sequencing if my miRNA sequencing library concentrations are too low to obtain a 4 nM library?
FAQ ID - 3666
表示
What method is used to eliminate adapter dimers from the QIAseq miRNA library?
FAQ ID - 3667
表示
Does a QIAseq miRNA library include hY4 Y RNA?
FAQ ID - 3670
表示
What is the recommended read length for libraries prepared using the QIAseq miRNA Library Kit?
FAQ ID - 3668
表示
How do Unique Molecular Indexes (UMIs) improve quantification?
FAQ ID - 3669
表示
What is the sequence of the QIAseq miRNA NGS 3’ Adapter?
FAQ ID - 3671
表示
What is the sequence of the QIAseq miRNA NGS 5’ Adapter?
FAQ ID - 3672
表示
What is the acceptable number of reads per sample per miRNA sequencing run?
FAQ ID - 3673
表示
Can you perform qPCR analysis of miRNAs from libraries prepared with the QIAseq miRNA Library Kit?
FAQ ID - 3674
表示
Which regions are covered by the GR DNAseq V2 Panels (#181900)?
FAQ ID - 3688
表示
What can be used to validate results obtained with the QIAseq miRNA Sequencing System?
FAQ ID - 3675
表示
When preparing plasma with the PAXgene Blood ccfDNA tubes, cat. # 768115, do you recommend that the first centrifugation step should be done with the brakes on or off?
FAQ ID - 3690
表示
Do the covered regions in the BED file include the primers?
FAQ ID - 3689
表示
How do I insert and replace an absorber strip into the PyroMark Q48 Autoprep chamber?
FAQ ID - 3691
表示
How much space does the PyroMark Q48 Autoprep instrument need?
FAQ ID - 3693
表示
Are peak heights of Q48 comparable to other PyroMark instruments?
FAQ ID - 3692
表示
Can unused wells in a pyrosequencing discs be used in the next run?
FAQ ID - 3694
表示
Where can I find the certificate of calibration for the Rotor-Disc OTV Kit (catalog number 981400)?
FAQ ID - 3695
表示
What is the minimum guaranteed shelf-life of the PAXgene Blood ccfDNA Tubes (100) (catalog no. 768115)?
FAQ ID - 3696
表示
What do the GTIN, UDI and REF abbreviations mean on the label of any QIAGEN box?
FAQ ID - 3697
表示
What methods are used during normalization of RNAseq data in the secondary GeneGlobe Data Analysis Center?
FAQ ID - 3698
表示
Do eluates generated with the PAXgene Blood miRNA Kit contain residual genomic DNA?
FAQ ID - 3637
表示
Can purification columns from other suppliers be processed on the QIAcube Connect?
FAQ ID - 141487
表示
Do I need to buy special kits for the QIAcube Connect?
FAQ ID - 141485
表示
Can I program my own protocols for the QIAcube Connect?
FAQ ID - 141486
表示
How can I get software updates for the QIAcube Connect?
FAQ ID - 141494
表示
Can the QIAcube Connect rotor and/or buckets be removed for cleaning?
FAQ ID - 141491
表示
Is it necessary to place the lids of the elution tube and column into the slots of the rotor adapter during processing on the QIAcube Connect?
FAQ ID - 141496
表示
Do I need to discard partially used QIAcube Connect tip racks?
FAQ ID - 141499
表示
How can I decontaminate the QIAcube Connect system?
FAQ ID - 141500
表示
How can I load new protocols onto the QIAcube Connect?
FAQ ID - 141501
表示
Can the QIAcube Connect heater/shaker be used independently from protocol runs?
FAQ ID - 141502
表示
What dedicated QIAcube Connect kits are available?
FAQ ID - 141504
表示
Where can I find the ordering information for QIAcube Connect accessories such as shaker rack plugs, rack labeling strips, reagent bottle racks, 30 ml reagent bottles, rotor-adapter holder, rotor adapters, sample tubes CB, sample tubes RB and spin-column adapter rings?
FAQ ID - 141505
表示
Do you have a protocol for the AllPrep DNA/RNA/Protein Mini Kit on the QIAcube Connect?
FAQ ID - 141506
表示
Do you have a protocol for the QIAprep Spin M13 Kit on the QIAcube Connect?
FAQ ID - 1414507
表示
Which QIAcube Connect standard protocol might be suitable to extract RNA from saliva or from a buccal cell pellet?
FAQ ID - 141508
表示
How often should the o-ring for the pipettor tip adapter be changed on the QIAcube Connect?
FAQ ID - 141509
表示
Can the CB and RB sample tubes be used interchangeably?
FAQ ID - 141510
表示
Why can I not find the Q-Base device in the device list during the first installation?
FAQ ID - 141516
表示
Which network settings are supported by the QIAcube Connect and Q-Base?
FAQ ID - 141517
表示
Why can’t I see my QIAcube Connect instrument in the QIAcube Connect App?
FAQ ID - 1414518
表示
Why is the QIAcube Connect App reacting so slowly?
FAQ ID - 141519
表示
Why are not all applications/kits/protocol files visible in the run setup (QIAcube Connect App)?
FAQ ID - 1414520
表示
Why does the connection test fail?
FAQ ID - 141522
表示
What is the required amount of input material per sample for the EpiTect Hi-C Kit?
FAQ ID -
143063
表示
What is the effect of using amounts of input material per sample that fall outside the recommended range?
FAQ ID -
143064
表示
How can I accurately determine the amount of input material for the EpiTect Hi-C Kit?
FAQ ID -
143065
表示
What sample source do you support?
FAQ ID -
143066
表示
How many reactions are in a kit?
FAQ ID -
143067
表示
How long does it take to complete the EpiTect Hi-C protocol?
FAQ ID -
143068
表示
Can I use cells that have been previously crosslinked and frozen (e.g., for a ChIP or ChIP-seq experiment) as input material for the EpiTect Hi-C protocol?
FAQ ID -
143069
表示
Can I substitute the endonuclease used in the Hi-C Digestion step with another endonuclease?
FAQ ID -
143070
表示
With which platform can I perform my sequencing?
FAQ ID -
143072
表示
Are there stopping points in the Hi-C workflow?
FAQ ID -
143071
表示
With which read length should the EpiTect Hi-C NGS libraries be sequenced
FAQ ID -
143073
表示
How do I know if my Hi-C sample is a good candidate for deep sequencing?
FAQ ID -
143074
表示
Does QIAGEN provide data analysis to accompany the EpiTect Hi-C Kit?
FAQ ID -
143075
表示
What kind of analysis does the EpiTect Hi-C Data Analysis Portal perform?
FAQ ID -
143076
表示
Does the EpiTect Hi-C Data Analysis Portal cost money?
FAQ ID -
143077
表示
Can I use my own pipeline to analyze results from my EpiTect Hi-C experiments?
FAQ ID -
143078
表示
How critical is the time of the temperature change from 60°C to 80°C?
FAQ ID -
143768
表示
Can the Repli-g Advanced DNA Single Cell Kit also be used for bacterial cells?
FAQ ID -
143079
表示
Why is DTT used only for semen samples?
FAQ ID -
143761
表示
Is it possible to use Lyse&Spin baskets?
FAQ ID -
143762
表示
Can the lysis volume be reduced for higher sensitivity?
FAQ ID -
143763
表示
What if only one heater shaker is available?
FAQ ID -
143764
表示
How long are sample lysates stable in the fridge/ freezer?
FAQ ID -
143765
表示
If 400 µl are used as lysis volume, how do I concentrate the lysate? (Otherwise the DNA would be too diluted.)
FAQ ID -
143766
表示
Why is the QIAamp Viral RNA Mini Kit (50) currently unavailable?
FAQ ID -147395
表示
Why is there no male DNA obtained from sexual assault samples?
FAQ ID -
143767
表示
What RNAs has QIAseq FastSelect been designed to remove?
FAQ ID -147910
表示
How does QIAseq FastSelect work?
FAQ ID -147907
表示
Is QIAseq FastSelect truly as easy as combining a reagent with RNA and ramping down the temperature?
FAQ ID -147909
表示
Will QIAseq FastSelect work in other species?
FAQ ID -147911
表示
What library prep kits has QIAseq FastSelect been tested with?
FAQ ID -147912
表示
I am using an RNA library prep kit that is not listed in the QIAseq FastSelect handbook. Will QIAseq FastSelect work with my kit?
FAQ ID -147913
表示
What RNA range has the QIAseq FastSelect been tested with?
FAQ ID -147914
表示
Can QIAseq FastSelect Plant or QIAseq FastSelect Yeast be combined with FastSelect 5S/16S/23S?
FAQ ID -147915
表示
Is it possible to test the efficiency of FastSelect rRNA removal by using a Bioanalyzer, etc.?
FAQ ID -147916
表示
How do I safely inactivate biohazardous flow-through material? 1 2
FAQ ID -12
表示
What are the expected DNA yields from different tissues using the QIAamp DNA Mini Kit? 8
FAQ ID -45
表示
How can I increase expression of my 6xHis-tagged protein in E. coli? 2
FAQ ID -63
表示
How can I decrease ribosomal RNA (rRNA) contamination using Oligotex?
FAQ ID -642
表示
動物細胞から細胞質 RNA を精製するためのプロトコールはありますか?
FAQ ID -1257
表示
kemot solk - Can cDNA prepared by any method be used as starting material in the ligation reaction of the QuantiTect Whole Transcriptome Kit? test
FAQ ID -1589
表示
次ページ
Back to top
Contact QIAGEN
Global contacts
Technical Service
Customer Care
FAQListPage