Frequently Asked Questions - FAQ



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アルファベット降順 Would co-transfection with the plasmid be expected to increase/decrease the transfection efficiency significantly? FAQ ID -3136 表示 With which read length should the EpiTect Hi-C NGS libraries be sequenced FAQ ID - 143073 表示 With which platform can I perform my sequencing? FAQ ID - 143072 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 Uracil-N-Glycosylase (UNG) completely remove contaminating amplicons when using QuantiTect +UNG Kits? FAQ ID -2139 表示 Will the sequences of the QuantiTect Primer Assays be provided? FAQ ID -804 表示 Will the sequence of the QuantiFast Probe Assays be provided? FAQ ID -2369 表示 Will the Reverse transcription control on the RT2 profiler PCR array work on any cDNA library? FAQ ID - 3534 表示 Will the REPLI-g UltraFast Mini Kit reaction always yield 10 µg DNA? FAQ ID -1328 表示 Will the random hexamers in the REPLI-g reaction interfere with downstream analysis? FAQ ID -713 表示 Will the Qproteome Plasma Membrane Protein Kit work with starting materials other than adherent mammalian cells? FAQ ID -1202 表示 Will the QIAxcel System run using a green Data Review Software Key? FAQ ID -1853 表示 Will the QIAquick PCR Purification Kit remove sufficient SYBR Green from real-time PCR reactions to allow sequencing? FAQ ID -637 表示 Will the primer sequence for the PyroMark CpG Assay be provided? FAQ ID -2823 表示 Will the PhosphoSerine antibody recognize Serine residues if the neighboring residues are Leucine or Isoleucine? FAQ ID -644 表示 Will the optimized DNA sequence for QIAgenes be provided? FAQ ID -2045 表示 Will the ligand in the Qproteome Plasma Membrane Protein protocol be specific for plasma membrane exclusively? FAQ ID -1198 表示 Will the FastLane Cell cDNA Kit work with suspension cells? FAQ ID -801 表示 Will the 2x QIAGEN Multiplex PCR Master Mix freeze at -20°C? FAQ ID - 525 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 Will TA cloning work with REPLI-g WGA product? FAQ ID -672 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 Rotor-Gene Kits also work on the Rotor-Gene 6000 and 3000 cyclers? FAQ ID -2121 表示 Will REPLI-g work at high temperatures? FAQ ID -656 表示 Will QuantiTect Primer Assays work with Rotor-Gene SYBR Green Kits using an annealing step at 60ºC? FAQ ID -2124 表示 Will QuantiTect Primer Assays work at an annealing temperature of 60ºC with QuantiFast SYBR Green PCR and RT-PCR Kits? FAQ ID -1553 表示 Will QIAseq FastSelect work in other species? FAQ ID -147911 表示 Will qBiomarker Copy Number Assays work with heterogeneous samples like mixtures of tumor and normal tissue? FAQ ID — 3419 表示 Will proteins eluted in the Qproteome Plasma Membrane Protein protocol be modified, e.g. with the ligand? FAQ ID -1195 表示 Will pipetting error affect the miRNA qPCR Assay results? FAQ ID -2728 表示 Will pipetting error affect the EpiTect Methyl qPCR Array results? FAQ ID -2741 表示 Will pancreas tissue swim on top of RNAprotect Tissue Reagent? FAQ ID -536 表示 Will mitochondrial DNA also be isolated using the DNA Tissue protocols on the QIAsymphony SP? FAQ ID -1921 表示 Will mitochondrial DNA also be isolated using the DNA tissue protocols and QIAsymphony DSP DNA Mini Kit on the QIAsymphony SP? FAQ ID -2991 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 Will dUTP in a PCR reaction affect pyrosequencing? FAQ ID -2843 表示 Will DNA from chromosomes collected in TE with a drop of mineral oil work with REPLI-g amplification? FAQ ID -664 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 Will acetone precipitation recommended in the Qproteome Protocols denature Protein? FAQ ID -807 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 should I work with diluted or undiluted screens? FAQ ID -2419 表示 Why should I use the RNeasy Microarray Tissue Mini Kit when purifying RNA for microarray analysis? FAQ ID -2188 表示 Why should I use the EpiTect Plus FFPE Bisulfite Kit instead of isolating FFPE DNA first and then doing the bisulfite conversion? FAQ ID -2412 表示 Why should I use RT² SYBR Green Mastermix with RT² qPCR Primer Assays? FAQ ID -2706 表示 Why should DNA or cDNA targets be less than 250 bp long for real-time PCR? FAQ ID-751 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 Why might Affymetrix GeneChip Mapping assays interfere with the REPLI-g FFPE kit? FAQ ID -1755 表示 Why is there RNA in the DNA eluate when using the AllPrep DNA Mini Spin Column? FAQ ID -1044 表示 Why is there no vacuum-only protocol for the RNeasy Plus 96 Kit? FAQ ID -1993 表示 Why is there no QuantiTect Primer Assay for my gene of interest? FAQ ID -1140 表示次ページ Back to top Contact QIAGEN Global contacts Technical Service Customer Care