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Why is a blood collection set required to collect blood into the PAXgene Blood ccfDNA Tube?
FAQ ID - 3628
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Can I use a different brand blood collection set with the PAXgene Blood ccfDNA Tube?
FAQ ID - 3630
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Can reagent from the PAXgene Blood ccfDNA Tube flow back into the patient’s arm?
FAQ ID - 3629
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What is the blood draw volume of the PAXgene Blood ccfDNA Tube
FAQ ID - 3631
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Where can I find the gene list for a specific RT² Profiler PCR Array?
FAQ ID - 3684
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Is it possible to store nucleic acids extracted using the SpeedXtract Virus Kit?
FAQ ID - 3680
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Can REPLI-g WGA be used to amplify cDNA if the cDNA is dsDNA (double-stranded DNA)?
FAQ ID - 3686
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What is the difference between RT² Profiler PCR Array and RT² Profiler PCR Array PLUS version?
FAQ ID - 3685
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I would like to stop during the library preparation procedure. When can I do that?
FAQ ID - 3687
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Should total RNA or small enriched RNA be used as the starting material for the QIAseq miRNA Library Kit?
FAQ ID - 3659
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Total RNA from what sample types are compatible with the QIAseq miRNA Library Kit?
FAQ ID - 3660
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Can miRNA sequencing libraries be prepared from total RNA isolated from heparinized plasma samples?
FAQ ID - 3661
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Are any components of the QIAseq miRNA Library Kit interchangeable with components from other QIAGEN kits?
FAQ ID - 3662
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What are recommended stopping points during the QIAseq miRNA Library Kit procedure?
FAQ ID - 3663
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When multiplexing samples, what sample indexes should be combined?
FAQ ID - 3664
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What is the maximum number of available sample indexes?
FAQ ID - 3665
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Can I still perform sequencing if my miRNA sequencing library concentrations are too low to obtain a 4 nM library?
FAQ ID - 3666
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What method is used to eliminate adapter dimers from the QIAseq miRNA library?
FAQ ID - 3667
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Does a QIAseq miRNA library include hY4 Y RNA?
FAQ ID - 3670
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What is the recommended read length for libraries prepared using the QIAseq miRNA Library Kit?
FAQ ID - 3668
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How do Unique Molecular Indexes (UMIs) improve quantification?
FAQ ID - 3669
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What is the sequence of the QIAseq miRNA NGS 3’ Adapter?
FAQ ID - 3671
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What is the sequence of the QIAseq miRNA NGS 5’ Adapter?
FAQ ID - 3672
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What is the acceptable number of reads per sample per miRNA sequencing run?
FAQ ID - 3673
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Can you perform qPCR analysis of miRNAs from libraries prepared with the QIAseq miRNA Library Kit?
FAQ ID - 3674
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Which regions are covered by the GR DNAseq V2 Panels (#181900)?
FAQ ID - 3688
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What can be used to validate results obtained with the QIAseq miRNA Sequencing System?
FAQ ID - 3675
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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
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Do the covered regions in the BED file include the primers?
FAQ ID - 3689
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How do I insert and replace an absorber strip into the PyroMark Q48 Autoprep chamber?
FAQ ID - 3691
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How much space does the PyroMark Q48 Autoprep instrument need?
FAQ ID - 3693
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Are peak heights of Q48 comparable to other PyroMark instruments?
FAQ ID - 3692
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Can unused wells in a pyrosequencing discs be used in the next run?
FAQ ID - 3694
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Where can I find the certificate of calibration for the Rotor-Disc OTV Kit (catalog number 981400)?
FAQ ID - 3695
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What is the minimum guaranteed shelf-life of the PAXgene Blood ccfDNA Tubes (100) (catalog no. 768115)?
FAQ ID - 3696
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What do the GTIN, UDI and REF abbreviations mean on the label of any QIAGEN box?
FAQ ID - 3697
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What methods are used during normalization of RNAseq data in the secondary GeneGlobe Data Analysis Center?
FAQ ID - 3698
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Do eluates generated with the PAXgene Blood miRNA Kit contain residual genomic DNA?
FAQ ID - 3637
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Can purification columns from other suppliers be processed on the QIAcube Connect?
FAQ ID - 141487
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Do I need to buy special kits for the QIAcube Connect?
FAQ ID - 141485
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Can I program my own protocols for the QIAcube Connect?
FAQ ID - 141486
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How can I get software updates for the QIAcube Connect?
FAQ ID - 141494
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Can the QIAcube Connect rotor and/or buckets be removed for cleaning?
FAQ ID - 141491
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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
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Do I need to discard partially used QIAcube Connect tip racks?
FAQ ID - 141499
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How can I decontaminate the QIAcube Connect system?
FAQ ID - 141500
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How can I load new protocols onto the QIAcube Connect?
FAQ ID - 141501
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Can the QIAcube Connect heater/shaker be used independently from protocol runs?
FAQ ID - 141502
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What dedicated QIAcube Connect kits are available?
FAQ ID - 141504
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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
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Do you have a protocol for the AllPrep DNA/RNA/Protein Mini Kit on the QIAcube Connect?
FAQ ID - 141506
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Do you have a protocol for the QIAprep Spin M13 Kit on the QIAcube Connect?
FAQ ID - 1414507
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Which QIAcube Connect standard protocol might be suitable to extract RNA from saliva or from a buccal cell pellet?
FAQ ID - 141508
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How often should the o-ring for the pipettor tip adapter be changed on the QIAcube Connect?
FAQ ID - 141509
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Can the CB and RB sample tubes be used interchangeably?
FAQ ID - 141510
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Why can I not find the Q-Base device in the device list during the first installation?
FAQ ID - 141516
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Which network settings are supported by the QIAcube Connect and Q-Base?
FAQ ID - 141517
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Why can’t I see my QIAcube Connect instrument in the QIAcube Connect App?
FAQ ID - 1414518
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Why is the QIAcube Connect App reacting so slowly?
FAQ ID - 141519
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Why are not all applications/kits/protocol files visible in the run setup (QIAcube Connect App)?
FAQ ID - 1414520
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Why does the connection test fail?
FAQ ID - 141522
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What is the required amount of input material per sample for the EpiTect Hi-C Kit?
FAQ ID -
143063
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What is the effect of using amounts of input material per sample that fall outside the recommended range?
FAQ ID -
143064
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How can I accurately determine the amount of input material for the EpiTect Hi-C Kit?
FAQ ID -
143065
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What sample source do you support?
FAQ ID -
143066
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How many reactions are in a kit?
FAQ ID -
143067
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How long does it take to complete the EpiTect Hi-C protocol?
FAQ ID -
143068
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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
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Can I substitute the endonuclease used in the Hi-C Digestion step with another endonuclease?
FAQ ID -
143070
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With which platform can I perform my sequencing?
FAQ ID -
143072
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Are there stopping points in the Hi-C workflow?
FAQ ID -
143071
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With which read length should the EpiTect Hi-C NGS libraries be sequenced
FAQ ID -
143073
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How do I know if my Hi-C sample is a good candidate for deep sequencing?
FAQ ID -
143074
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Does QIAGEN provide data analysis to accompany the EpiTect Hi-C Kit?
FAQ ID -
143075
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What kind of analysis does the EpiTect Hi-C Data Analysis Portal perform?
FAQ ID -
143076
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Does the EpiTect Hi-C Data Analysis Portal cost money?
FAQ ID -
143077
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Can I use my own pipeline to analyze results from my EpiTect Hi-C experiments?
FAQ ID -
143078
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How critical is the time of the temperature change from 60°C to 80°C?
FAQ ID -
143768
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Can the Repli-g Advanced DNA Single Cell Kit also be used for bacterial cells?
FAQ ID -
143079
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Why is DTT used only for semen samples?
FAQ ID -
143761
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Is it possible to use Lyse&Spin baskets?
FAQ ID -
143762
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Can the lysis volume be reduced for higher sensitivity?
FAQ ID -
143763
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What if only one heater shaker is available?
FAQ ID -
143764
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How long are sample lysates stable in the fridge/ freezer?
FAQ ID -
143765
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If 400 µl are used as lysis volume, how do I concentrate the lysate? (Otherwise the DNA would be too diluted.)
FAQ ID -
143766
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Why is the QIAamp Viral RNA Mini Kit (50) currently unavailable?
FAQ ID -147395
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Why is there no male DNA obtained from sexual assault samples?
FAQ ID -
143767
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What RNAs has QIAseq FastSelect been designed to remove?
FAQ ID -147910
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How does QIAseq FastSelect work?
FAQ ID -147907
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Is QIAseq FastSelect truly as easy as combining a reagent with RNA and ramping down the temperature?
FAQ ID -147909
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Will QIAseq FastSelect work in other species?
FAQ ID -147911
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What library prep kits has QIAseq FastSelect been tested with?
FAQ ID -147912
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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
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What RNA range has the QIAseq FastSelect been tested with?
FAQ ID -147914
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Can QIAseq FastSelect Plant or QIAseq FastSelect Yeast be combined with FastSelect 5S/16S/23S?
FAQ ID -147915
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Is it possible to test the efficiency of FastSelect rRNA removal by using a Bioanalyzer, etc.?
FAQ ID -147916
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How do I safely inactivate biohazardous flow-through material? 1 2
FAQ ID -12
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What are the expected DNA yields from different tissues using the QIAamp DNA Mini Kit? 8
FAQ ID -45
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How can I increase expression of my 6xHis-tagged protein in E. coli? 2
FAQ ID -63
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How can I decrease ribosomal RNA (rRNA) contamination using Oligotex?
FAQ ID -642
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Do you have a protocol for purification of cytoplasmic RNA from animal cells?
FAQ ID -1257
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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
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