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I cannot see the LCD display fonts on the Sigma Centrifuge. How do I adjust the contrast?
FAQ ID -822
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I left Buffer P1 at room temperature after addition of RNase A, what shall I do?
FAQ ID -859
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How long does a typical in vitro translation reaction take with your large-scale EasyXpress protein synthesis kits?
FAQ ID -880
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How much protein can be produced with the EasyXpress Protein Synthesis Mega Kit?
FAQ ID -843
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Do you have a protocol for the isolation of very low-copy plasmids from Streptomyces spp.?
FAQ ID -893
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Do you have a protocol for the isolation of plasmid DNA from Citrobacter freundii?
FAQ ID -885
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Do you have a protocol for the isolation of plasmid DNA from Corynebacterium glutamicum?
FAQ ID -886
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Do you have a protocol for the isolation of plasmid DNA from Agrobacterium?
FAQ ID -898
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Do you have a protocol for the isolation of plasmid DNA from Borrelia spp.?
FAQ ID -884
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Do you have a protocol for the isolation of plasmid DNA from Bacillus subtilis?
FAQ ID -896
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Do you have a protocol for the isolation of plasmid DNA from yeast?
FAQ ID -853
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Do you have a protocol for the isolation of plasmid DNA from Lactobacillus spp.?
FAQ ID -887
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Do you have a protocol for the isolation of single-stranded DNA from M13 phage using QIAGEN Plasmid Kits?
FAQ ID -894
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Do you have a protocol for the isolation of plasmid DNA from Staphylococcus spp.?
FAQ ID -890
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Do you have a protocol for the isolation of plasmid DNA from Oligotropha carboxidovorans?
FAQ ID -888
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Do you have a protocol for the isolation of plasmid DNA from Proteus spp.?
FAQ ID -889
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What are the most commonly used protease inhibitors?
FAQ ID -53
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How should I quantify RNA isolated with RNeasy Kits?
FAQ ID -32
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Is plasmid DNA purified with QIAGEN Plasmid Purification Kits suitable for in vitro transcription?
FAQ ID -1
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How should I propagate pQE expression plasmids?
FAQ ID -58
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What are the compatibilities of different reagents with Ni-NTA matrices?
FAQ ID -49
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How is "Touchdown PCR" used to increase PCR specificity?
FAQ ID -75
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What should the starting template DNA quality and quantity be for PCR?
FAQ ID -74
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Why do I get smeared PCR products?
FAQ ID -87
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Why does my isolated RNA have a low OD 260/280 ratio?
FAQ ID -97
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When is chloramphenicol amplification of plasmids performed?
FAQ ID -3
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How can I remove imidazole from a protein sample?
FAQ ID -91
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How can I increase the amount of soluble recombinant protein in E. coli expression?
FAQ ID -64
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How can I avoid little or no RNA yields when using an RNeasy Kit?
FAQ ID -28
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What are the restriction sites of the pDrive Vector in the QIAGEN PCR Cloning Kit?
FAQ ID -160
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What are the molecular weights of proteins in the 6xHis Protein Ladder?
FAQ ID -169
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What are your recommendations for cotransfecting several plasmids?
FAQ ID -124
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What is the composition of Buffer EB?
FAQ ID -199
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Is mRNA isolation necessary for sensitive RT-PCR?
FAQ ID -111
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What are the recommended culture and buffer volumes for a very low-copy plasmid?
FAQ ID -168
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Should I use Ni-NTA Agarose in column or batch format for purification of 6xHis-tagged proteins?
FAQ ID -147
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What is the difference between disruption and homogenization in the RNeasy System?
FAQ ID -139
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Which Anti-His Antibody is the most sensitive for my protein of interest?
FAQ ID -172
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When should carrier be used with the QIAamp DNA Mini or the DNeasy Blood & Tissue Kit?
FAQ ID -100
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Why do I have to add beta-mercaptoethanol (beta-ME) to lysis Buffer RLT of the RNeasy Kits?
FAQ ID -101
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What is the recommended culture medium for the QIAprep System?
FAQ ID -154
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What is the RNase A concentration and composition of Buffer P1?
FAQ ID -198
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What is the genotype of the EZ Competent Cells?
FAQ ID -157
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What kind of PCR products can be cloned with the QIAGEN PCR Cloning Kit?
FAQ ID -165
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What is the principle behind Effectene Transfection Reagent?
FAQ ID -184
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What is the size of genomic DNA that is obtained with QIAGEN Genomic-tips?
FAQ ID -142
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How can I eliminate contaminating protein in my Ni-NTA 6xHis-tag protein purification?
FAQ ID -102
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How can I purify very small amounts of 6xHis-tagged protein using Ni-NTA technology?
FAQ ID -134
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How can I improve recoveries when using the QIAquick Kits?
FAQ ID -180
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How can I extract DNA from a polyacrylamide (PAGE) gel?
FAQ ID -120
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How can I improve ligation efficiency of DNA from a QIAEX II Gel Extraction Kit?
FAQ ID -141
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How can I isolate RNA from 1 gram of plant tissue?
FAQ ID -128
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How can I improve the performance of the HiSpeed QIAprecipitator module?
FAQ ID -144
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How can I improve transfection efficiency using Effectene Transfection Reagent?
FAQ ID -181
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What can I use to isolate RNA smaller than 200 nucleotides?
FAQ ID -115
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What epitopes do the Anti-His Conjugates and Anti-His Antibodies recognize?
FAQ ID -170
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What are the maximum culture volumes to use with the QIAGEN Plasmid Midi or Maxi Kit?
FAQ ID -167
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How should RNeasy Kits be stored and how long are they stable?
FAQ ID -103
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Is it possible to cleave the 6xHis-tag from an expressed protein?
FAQ ID -140
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How should I store plant material for DNA isolation using the DNeasy Plant Kit?
FAQ ID -114
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How should QIAGEN Plasmid Purification Kits be stored and for how long?
FAQ ID -192
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What are the features and benefits of the QIAexpress 6xHis Tag System?
FAQ ID -193
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What is the small band below my fragment of interest on an agarose gel after DNA cleanup using QIAquick?
FAQ ID -148
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Do you have transfection data for QIAGEN Transfection Reagents?
FAQ ID -158
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Do I need to use an RNase inhibitor in my RT reaction?
FAQ ID -119
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Do you have data showing effects of sample size on DNA yield and purity using the DNeasy 96 Blood & Tissue kit?
FAQ ID -129
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How can I avoid variable transfection efficiencies with SuperFect Reagent?
FAQ ID -179
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Does QIAGEN offer vectors for direct cloning of PCR products?
FAQ ID -146
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Can a QIAquick Gel Extraction Kit be used to obtain RNA from a formaldehyde gel?
FAQ ID -133
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Are QIAamp DNA isolation kits suitable for apoptosis studies?
FAQ ID -149
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Can DyeEx be used to clean up labeled DNA other than sequencing templates?
FAQ ID -137
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Are RNeasy spin columns sold separately?
FAQ ID -159
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Can I use QIAprep Miniprep kits for low-copy plasmids and cosmids?
FAQ ID -127
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Can I use the QIAquick PCR Purification Kit for restriction enzyme cleanup?
FAQ ID -130
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Can I use a QIAfilter Cartridge for purifying large plasmids?
FAQ ID -121
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Can I use Omniscript or Sensiscript RT's at a higher temperature?
FAQ ID -116
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How does imidazole affect my quantitation of protein?
FAQ ID -132
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How can I optimize the transfection of oligos and large plasmids using PolyFect Transfection Reagent?
FAQ ID -176
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How do you ensure that RNeasy buffers are RNase-free?
FAQ ID -113
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How can I purify DNA from soil, food and sewage samples for PCR?
FAQ ID -118
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How can I obtain DNA-free RNA using an RNeasy Midi or Maxi Kit?
FAQ ID -143
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How do I prepare an insert for pQE vectors?
FAQ ID -185
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How should I store Anti·His and Tag·100 Antibodies?
FAQ ID -194
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Do you have a protocol for purification of total DNA from insects?
FAQ ID -1254
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Is your Nuclease-Free Water fluorescence-free?
FAQ ID -1291
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Do you have a protocol for purification of total DNA from crude lysates?
FAQ ID -1255
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How should the GelPilot DNA Loading Dye be handled?
FAQ ID -1287
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What quality level does your Nuclease-Free Water have?
FAQ ID -1292
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What is the pH value of QIAGEN's Nuclease-Free Water?
FAQ ID -1290
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Does GelPilot DNA Loading Dye contain ethidium bromide?
FAQ ID -1286
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Are MaXtract tubes siliconized?
FAQ ID -1298
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Can phenol/chloroform be placed in the MaXtract tube for extraction at a later time?
FAQ ID -1299
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Should I input the dilution factor of my samples into the LiquiChip Analyser Software dilution factors of samples?
FAQ ID -1211
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What cell lines have been tested with the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1205
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What are the new features of the EasyXpress Insect Kit II compared to the original Protein Synthesis Insect kit?
FAQ ID -1220
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What are your recommendations for PCR template preparation for use with the EasyXpress Insect Kit II?
FAQ ID -1221
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Is it possible to increase nucleic acid concentrations when following protocols on the BioRobot EZ1?
FAQ ID -1232
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Is a saliva collection device provided in the RNeasy Protect Saliva Mini Kit?
FAQ ID -1213
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How should I prepare buffy coat samples for use on the BioRobot EZ1?
FAQ ID -1249
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Is it possible to use QIAGEN's pQE-Trisystem Vector with the EasyXpress Insect Kit II?
FAQ ID -1225
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Is training of lab personnel included with the purchase of a BioRobot EZ1?
FAQ ID -1239
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Where can I find information about the worktable setup on the BioRobot EZ1?
FAQ ID -1243
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Is RNAprotect Cell Reagent provided in the RNeasy Protect Cell Kit available separately?
FAQ ID -1217
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What vector do you recommend as template for in-vitro protein expression with the EasyXpress Insect Kit II?
FAQ ID -1224
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What type of promoter should my template have for in-vitro protein expression with the EasyXpress Insect Kit II?
FAQ ID -1223
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What is the difference between various FlexiTube siRNAs listed for the same target gene, and which one should I choose?
FAQ ID -1206
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Will the Qproteome Plasma Membrane Protein Kit work with starting materials other than adherent mammalian cells?
FAQ ID -1202
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What disposables are required for nucleic acid isolations on the BioRobot EZ1?
FAQ ID -1246
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What is the protein yield when using the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1201
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What is the maximum number of cells that can be used with the AllPrep RNA/Protein Kit ?
FAQ ID -1208
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Do the foils sealing the EZ1 Reagent Cartridges have to be manually removed prior to loading the robot?
FAQ ID -1240
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What is the smallest and the largest protein that you tested for expression with the EasyXpress Insect Kit II?
FAQ ID -1218
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What is the size of the BioRobot EZ1?
FAQ ID -1245
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Does anything have to be added to express post-translational modifications (PTMs) with the EasyXpress Insect Kit II?
FAQ ID -1226
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Do you have a protocol for isolating cytoplasmic RNA from animal cells using the RNeasy Mini Kit?
FAQ ID -1207
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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
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Do you have a protocol for purification of cytoplasmic RNA from animal cells?
FAQ ID -1257
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Can cells stabilized with RNAprotect Cell Reagent be used for cell sorting by flow cytometry (FACS)?
FAQ ID -1216
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Can glycosylated proteins be expressed using the EasyXpress Insect Kit II?
FAQ ID -1227
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Can the Strep-Tactin Magnetic Beads of the Qproteome Plasma Membrane Protein Kit be reused?
FAQ ID -1204
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Can RNAprotect Saliva Reagent be purchased separately?
FAQ ID -1214
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Can you recommend a Reagent or Kit for stabilizing RNA in cultured cells?
FAQ ID -1215
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Can the RLT lysate of the BioSprint DNA Plant protocol be stored frozen?
FAQ ID -1248
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Can the Qproteome Plasma Membrane Protein Kit be used with tissue samples?
FAQ ID -1200
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How can we get our BioRobot EZ1 upgraded when new protocols are launched?
FAQ ID -1241
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How can I decontaminate the BioRobot EZ1?
FAQ ID -1231
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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
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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
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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
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Do you have a protocol for transfection of differentiated macrophage cell lines (THP) with siRNA?
-1
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Do you have a protocol for transfection of macrophage cell lines (J774.A1 and RAW 264.7) with siRNA?
FAQ ID -1251
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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
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Can the PAXgene Blood RNA Tubes undergo freeze/thaw cycles?
FAQ ID -2471
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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
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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
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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
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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
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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
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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
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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
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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
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What is the recommended amplicon size for CpG assays?
FAQ ID -2825
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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
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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
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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
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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
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What is the composition of Buffer PKD?
FAQ ID -2801
表示
What is the composition of Buffer APP?
FAQ ID -2804
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What is the composition of Buffer ALO?
FAQ ID -2805
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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
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What is the sensitivity limitation for pyrosequencing?
FAQ ID -2840
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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
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How do I find the SureSilencing shRNA Plasmids for my gene of interest?
FAQ ID -2883
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How do I prevent a drifting baseline in my pyrosequencing pyrogram?
FAQ ID -2878
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How are the SureSilencing shRNA Plasmids shipped?
FAQ ID -2884
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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
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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
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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
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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
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How many cells can be used with the Qproteome Mitochondria Isolation Kit, and how much mitochondrial protein can be expected?
FAQ ID -1189
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How many drops can be set up on a protein crystallization support?
FAQ ID -1110
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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
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