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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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