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		QIAGEN CLC Genomics Workbench 20 – scalable desktop software for NGS data analysis Show details
		Using the microbiome to unlock the secrets of forensic evidence: classification of the body source of human traces Show details
		When is chloramphenicol amplification of plasmids performed? FAQ ID -3 Show details
		How can I increase the amount of soluble recombinant protein in E. coli expression? FAQ ID -64 Show details
		What is the difference between disruption and homogenization in the RNeasy System? FAQ ID -139 Show details
		How can I check for purity of RNA isolated using RNeasy Kits? FAQ ID -1023 Show details
		What does transcript variant mean when searching for specific QuantiTect Primer Assays? FAQ ID -1137 Show details
		Is a weak or late (high) CT value of the IC an indicator for PCR inhibition? FAQ ID -1398 Show details
		The concentrations of the quantitation standards (QS) of several artus® kits are stated as IU/µl (international units per µl). Is it possible to convert this concentration unit into copies per µl? FAQ ID -1501 Show details
		Why is the IC not detectable although the analytical PCR is negative? FAQ ID -1506 Show details
		How often should the Crosstalk Colour Compensation (ccc) be carried out? Where does the ccc file have to be saved? FAQ ID -1512 Show details
		What is qPCR? FAQ ID -2668 Show details
		What positive controls are typically included in qPCR and/or qRT-PCR experiments? FAQ ID -2673 Show details
		What is the delta Rn value? FAQ ID -2681 Show details
		Why do I see multiple high-intensity peaks in my qPCR dissociation curve at temperatures less than 70 ºC? FAQ ID -2690 Show details
		How do you design your EpiTect ChIP qPCR Assay primers? Do they work with SB GR? FAQ ID -2749 Show details
		How can I keep my centrifuge tubes endotoxin-free? FAQ ID -301 Show details
		What is needed for performing delta delta Ct relative quantitation on the Rotor-Gene Q? FAQ ID -3178 Show details
		Can the miScript II RT Kit be used to quantify plant miRNAs? FAQ ID - 3431 Show details
		What methods are used during normalization of RNAseq data in the secondary GeneGlobe Data Analysis Center? FAQ ID - 3698 Show details
		What is a QIAshredder? Is it sufficient for complete disruption and homogenization of my tissue sample? FAQ ID -631 Show details
		Why does the QIAamp DNA Mini Tissue Protocol require both ATL and AL buffer, while the Blood Protocol only uses AL? FAQ ID -633 Show details
		I ran my RNA out on an agarose gel and can see lots of bands similar to a ladder. Why? FAQ ID -745 Show details
		How can I get a certificate for quality assurance (ISO 13485 and ISO 9001) from QIAGEN? FAQ ID -762 Show details
		How can I separate PCR fragments that are small and very close in size on an agarose gel? FAQ ID -800 Show details
		How can I increase expression of my 6xHis-tagged protein in E. coli? FAQ ID -63 Show details
		Do I need to buy special kits for the QIAcube Connect MDx? 148725 Show details
		Can the QIAcube rotor and/or buckets be removed for cleaning? 148731 Show details
		How can I decontaminate the QIAcube Connect MDx system? 148739 Show details
		How can I load new protocols onto the QIAcube Connect MDx? 148740 Show details
		Can the QIAcube Connect MDx heater/shaker be used independently from protocol runs? 148741 Show details
		Can the QIAcube Connect MDx centrifuge be used independently from protocol runs? 148742 Show details
		What are recommended stopping points in the procedure of the QIAamp DNA FFPE Advanced Kits? 153892 Show details
		Can I use a custom master mix instead of a QIAGEN master mix? FAQ ID - 9211 Show details
		Is it necessary to reanalyze a plate with VPF (Volume Precision Factor) that was already processed using a QIAcuity instrument that was purchased in 2020? 3771 Show details
		Can I use a custom master mix instead of a QIAGEN master mix? 3777 Show details
		Is it necessary to reanalyze a plate with VPF (Volume Precision Factor) that was already processed using a QIAcuity instrument that was purchased in 2020? FAQ ID - 9205 Show details
		What are recommended stopping points in the procedure of the EZ1&2 DNA FFPE Kits? 3753 Show details
		What is the additive in PAXgene Blood DNA Tubes (IVD)? FAQ ID - 3372 Show details
		Can I buy the RNeasy Mini columns, RNeasy MinElute columns, RNeasy Midi columns or the RNeasy Maxi columns separately? FAQ ID - 3388 Show details
		What is in the additive in the PAXgene Saliva Collector? 3810 Show details
		I left Buffer P1 at room temperature after addition of RNase A, what shall I do? FAQ ID -859 Show details
		How long can blood samples be stored before sample preparation using the EZ1 DSP DNA Blood system? FAQ ID -1565 Show details
		Can the QIAcube heater/shaker be used independently from protocol runs? FAQ ID -1422 Show details
		When should the Normalization protocol be used? FAQ ID -1155 Show details
		How can I decontaminate the QIAcube system? FAQ ID -1419 Show details
		Can the QIAcube rotor and/or buckets be removed for cleaning? FAQ ID -1410 Show details
		Can the QIAcube centrifuge be used independently from protocol runs? FAQ ID -1423 Show details
		Do I need to buy special kits for the QIAcube? FAQ ID -1402 Show details
		What are the advantages of EnzScript M-MLV Reverse Transcriptase RNase H- (P7600) versus wild type M-MLV Reverse Transcriptase (P7040)? FAQ ID - 3960 Show details
		What PCR enzymes can be used following first-strand synthesis? FAQ ID - 3963 Show details
		On which instrumentation will the RT² Profiler PCR Array work? FAQ ID -2719 Show details
		Can I use REPLI-g for SNP Genotyping? FAQ ID -700 Show details
		How is "Touchdown PCR" used to increase PCR specificity? FAQ ID -75 Show details
		What should the starting template DNA quality and quantity be for PCR? FAQ ID -74 Show details
		Why do I get smeared PCR products? FAQ ID -87 Show details

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