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Which kits can be used in combination with the PyroMark CpG Assays and PyroMark Custom Assays?
FAQ ID -2822
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What region of LINE gets targeted by the assay for PyroMark Q96 MD or PyroMark Q24?
-1
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What should be the single peak height for the PyroMark Control Oligo on the different PyroMark instruments?
FAQ ID -2852
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Does the same U1 promoter in the SureSilencing shRNA Plasmids express shRNA in human, mouse, and rat cell lines?
FAQ ID -2887
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What is the amplicon length of the PyroMark CpG LINE assay?
-1
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How are the PyroMark CpG Assays reconstituted?
FAQ ID -2817
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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
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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
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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
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Can I directly transfect SureSilencing shRNA Plasmids into my cells?
FAQ ID -2899
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Can I order the nucleotides from PyroMark Gold Reagents separately?
FAQ ID -2827
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Do any of the SureSilencing shRNA Plasmids contain inducible promoters?
FAQ ID -2888
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Does QIAGEN offer a design of Custom PyroMark CpG Assays?
FAQ ID -2818
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Can unused wells in a pyrosequencing plate be used in the next run?
FAQ ID -2872
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Can PyroMark Gold reagents be vortexed?
FAQ ID -2844
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Can the PyroMark Q96 CpG LINE assay be used with an ID system?
-1
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What are the features of PyroMark CpG Assays e.g. in terms of design, validation?
FAQ ID -2821
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How do I reduce background peaks in the pyrosequencing pyrogram?
FAQ ID -2877
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What are the features of the new PyroMark Q96 ID software 2.5?
FAQ ID -2867
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What are the changes of PyroMark Assay Design Software Version 2.0 compared to 1.0?
FAQ ID -2849
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Is there a user manual available for the PyroMark Assay design software?
FAQ ID -2851
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Should I use the SureSilencing shRNA Plasmids with the neomycin-resistance marker, the puromycin-resistance marker, or the GFP reporter gene?
FAQ ID -2882
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What else do I need to complete an experiment using the SureSilencing shRNA Plasmids?
FAQ ID -2889
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What cell line does QIAGEN use for quality control testing of the SureSilencing shRNA Plasmids?
FAQ ID -2885
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What is included in a PyroMark Custom Assay?
FAQ ID -2815
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What cell lines can I use with the SureSilencing shRNA Plasmids?
FAQ ID -2891
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How many nucleotides of a homopolymer can be resolved in pyrosequencing?
FAQ ID -2871
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What concentration should be used for the sequencing primer in pyrosequencing?
FAQ ID -2826
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How many CpG sites are analyzed by the PyroMark CpG LINE assay?
-1
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How do I set up a PyroMark CpG Assay?
FAQ ID -2814
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How long should I wait after transfection before enriching my transfected cells, validating knock down, and looking for phenotypic changes?
FAQ ID -2893
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How many times can the cartridges for Pyromark Q24 or PyroMark Q96 ID instruments are reused?
FAQ ID -2863
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Is the CpG software included in the PyroMark instruments to study methylation status?
FAQ ID -2842
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Is the expression level of miRNA precursors lower compared to that of mature miRNAs?
FAQ ID -2807
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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
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How many times can vacuum troughs be re-used with the PyroMark Vacuum Preparation Stations?
FAQ ID -2848
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What is the meaning of the abbreviations NDT and CDT and what are the differences?
FAQ ID -2841
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What is the PyroMark Q96 Data Converter?
FAQ ID -2868
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What is the composition of RBC Lysis Solution?
FAQ ID -2808
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What is the concentration of PyroMark Control Oligo?
FAQ ID -2846
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What is the pyrosequencing data exchange tool for?
FAQ ID -2864
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What is the reason for signals ceasing in the middle of a pyrosequencing run?
FAQ ID -2875
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What is the reason for split peaks appearing in between dispensations on my pyrosequencing pyrogram?
FAQ ID -2881
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What is the reason for a high substrate peak in the pyrosequencing pyrogram?
FAQ ID -2879
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What is the composition of Buffer FRN?
FAQ ID -2802
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What is the composition of Buffer PKD?
FAQ ID -2801
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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
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Which analyses can be performed with the PyroMark Q96 MD software?
FAQ ID -2866
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Will dUTP in a PCR reaction affect pyrosequencing?
FAQ ID -2843
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Will the primer sequence for the PyroMark CpG Assay be provided?
FAQ ID -2823
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What is the use of the PyroMark Q24 Validation Oligo?
FAQ ID -2855
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Which purity grade is recommended for pyrosequencing primers?
FAQ ID -2832
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Which PyroMark Gold Q96 Reagent should be used for which instrument and application?
FAQ ID -2836
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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
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What primers may I use to sequence the shRNA cassette within the SureSilencing shRNA Plasmids?
FAQ ID -2886
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Where can I order the Streptavidin Sepharose beads for pyrosequencing?
FAQ ID -2850
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Where to find explanations to the warning given by the PyroMark software after run data analysis?
FAQ ID -2874
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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
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Does the PyroMark CpG LINE assay target mouse transposons as well?
-1
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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
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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
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Is it possible to collect intact mitochondria before or after the density gradient centrifugation step of the Qproteome Mitochondria Isolation protocol?
FAQ ID -1187
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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
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What EZ1 DNA Investigator protocol is recommended for very precious samples?
FAQ ID -1154
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What cell lines have been tested with the Fastlane Cell cDNA Kit?
FAQ ID -1175
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What does transcript variant mean when searching for specific QuantiTect Primer Assays?
FAQ ID -1137
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What does 'QIAGEN Certified Solution' for Protein Crystallization mean?
FAQ ID -1121
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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
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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
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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
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In which formats are crystallization condition Screening Suites available?
FAQ ID -1127
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If a QuantiTect Primer Assay has more than one version number, does this mean that earlier assay versions may not work?
FAQ ID -1136
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How sensitive is the LiquiChip Reader?
FAQ ID -1157
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What is a QuantiTect Primer Assay?
FAQ ID -1141
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How much time is needed for a LiquiChip assay point measurement?
FAQ ID -1162
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What is the delivery time for QuantiTect Primer Assays?
FAQ ID -1142
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What kind of strategy for initial screening of protein crystallization conditions do you recommend?
FAQ ID -1120
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Why are there various different QuantiTect Primer Assays for my gene (previous versions, transcript variants)?
FAQ ID -1133
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When should the EZ1 DNA Investigator Normalization protocol be used?
FAQ ID -1155
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Where can I find the composition tables for solutions used in individual Crystallization Screening Suites?
FAQ ID -1124
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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
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Can the EZ1 DNA Investigator Tip Dance protocol cope with any solid matrix remaining in the sample tube?
FAQ ID -1153
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What type of magnet do you recommend for handling the magnetic beads in the Qproteome Plasma Membrane Protein protocol?
FAQ ID -1193
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What starting material can be used with the Qproteome Mitochondria Isolation Kit?
FAQ ID -1184
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Are EasyXtal 15-Well Tools stackable?
FAQ ID -1116
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Which QuantiTect Primer Assay should I choose for my gene of interest?
FAQ ID -1135
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Why can I not find the QuantiTect Primer Assay in GeneGlobe that I had previously ordered from QIAGEN?
FAQ ID -1138
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Which chemical products do you use to prepare screening solutions for protein crystallization?
FAQ ID -1122
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Will proteins eluted in the Qproteome Plasma Membrane Protein protocol be modified, e.g. with the ligand?
FAQ ID -1195
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Why does the QuantiTect Primer Assay for my gene of interest have only one version number?
FAQ ID -1134
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Will the ligand in the Qproteome Plasma Membrane Protein protocol be specific for plasma membrane exclusively?
FAQ ID -1198
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Will integral, peripheral as well as lipid-anchored plasma membrane proteins be isolated with the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1199
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Why is there no QuantiTect Primer Assay for my gene of interest?
FAQ ID -1140
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What is the dynamic range of detection of the LiquiChip Reader?
FAQ ID -1158
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What is the EasyXtal 15-Well Tool made of?
FAQ ID -1106
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Can the nuclei and cell debris fraction generated in the QProteome Mitochondria isolation procedure be used for further fractionation?
FAQ ID -1185
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Can the EZ1 DNA Forensic Card be used with the EZ1 DNA Investigator Kit?
FAQ ID -1151
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Can the EasyXtal 15-Well Tools be reused?
FAQ ID -1117
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Can the Qproteome Plasma Membrane Protein Kit be used with suspension cells?
FAQ ID -1194
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Can your Tag antibody recognize rat MAPK1 also?
-100
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Can the remaining fractions obtained in the Qproteome Plasma Membrane Protein procedure be used in downstream assays?
FAQ ID -1197
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Can xMAP kits from other Luminex partners be used on the LiquiChip System purchased from QIAGEN?
FAQ ID -1156
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Can the Spin Columns of the Qproteome Albumin/IgG Depletion Kit be reused?
FAQ ID -1173
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Are protein modifications such as glycosylation problematic when using the Qproteome Plasma Membrane Protein Kit?
FAQ ID -1196
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Are scoring sheets available for each crystallization condition Screening Suite?
FAQ ID -1125
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Can mitochondria separated with the Qproteome Mitochondria Isolation Kit be used for downstream DNA isolation?
FAQ ID -1188
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Can acetone be used for precipitation of protein from Buffer RLT lysates generated with RNeasy Kits?
FAQ ID -1164
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Can I increase the annealing temperature recommended for QuantiTect Primer Assays used with the QuantiTect SYBR Green PCR Kits?
FAQ ID -1146
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Does the EasyXtal Tool conform to an SBS format?
FAQ ID -1115
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How are NeXtal deep-well blocks sealed? Can they be resealed?
FAQ ID -1128
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Do you have WGA protocols for starting materials not mentioned in the REPLI-g Handbooks?
FAQ ID -1160
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Do you have a protocol for the isolation of genomic DNA from whole blood for use in MRC-Holland MLPA® assays?
FAQ ID -1169
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Do you have a protocol for the purification of 6xHis-tagged proteins using BioSprint?
FAQ ID -1167
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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
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How is the quality of the crystallization condition Screening Suites guaranteed?
FAQ ID -1126
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How do I use EasyXtal Crystallization Tools?
FAQ ID -1105
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How did you determine that your AllStar Negative Control siRNA binds to RISC?
FAQ ID -1180
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How does the sealing efficiency of the crystallization supports of the EasyXtal 15-Well Tool compare to grease?
FAQ ID -1109
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Do you have a kit for protein isolation from mitochondria prepared with your Qproteome Mitochondria Isolation Kit?
FAQ ID -1190
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Do you have a kit for the isolation of RNA from formalin-fixed, paraffin-embedded samples?
FAQ ID -1174
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Do QuantiTect Primer Assays contain SYBR Green dye?
FAQ ID -1143
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Do I need an ultracentrifuge for the density gradient centrifugation step in the Qproteome Mitochondria Isolation protocol?
FAQ ID -1186
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Do protein crystals stick to the walls of cavities when using the DropGuard crystallization supports?
FAQ ID -1108
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Do you have a protocol for evaluating pipetting accuracy of the BioRobot EZ1?
FAQ ID -1131
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Do you have a protocol for purification of DNA from stool samples for pathogen detection using BioSprint Instruments?
FAQ ID -1165
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Do you have a protocol for purification of DNA from stool samples using BioSprint Instruments?
FAQ ID -1166
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Do you have a protocol for evaluating temperature accuracy of the BioRobot EZ1?
FAQ ID -1168
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How can I analyze proteins from exosomes and other extracellular vesicles (EVs) obtained with the exoEasy Maxi Kit by SDS-PAGE?
FAQ ID - 3707
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What is the concentration of SureENTRY Transduction Reagent?
FAQ ID - 3708
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Is it possible to modify the transduction protocol for Cignal Lenti Reporter Assays to save some pipetting steps?
FAQ ID - 3709
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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
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Can I store the QIAseq Beads of the QIAseq Targeted DNA Panel at -20°C?
FAQ ID - 3711
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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
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What sample tubes can I use on my QIAsymphony SP system?
FAQ ID - 3713
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How can I decontaminate my QIAsymphony SP / AS system?
FAQ ID - 3714
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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
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Can I use carrier RNA with the RNeasy UCP Micro Kit (cat. no. 73934)?
FAQ ID - 3716
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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
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How is the Pyromark Q48 cartridge to be cleaned?
FAQ ID - 3718
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Can the disc and absorber strips for the Pyromark Q48 be reused?
FAQ ID - 3720
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What is the dead volume of the cartridges in PyroMark Q48?
FAQ ID - 3719
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How much DNA is needed in the PyroMark Q48?
FAQ ID - 3721
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Can I transfer my assays from PyroMark Q24/Q96 to PyroMark Q48 Autoprep?
FAQ ID - 3723
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Can I use PyroMark Q48 for diagnostics?
FAQ ID - 3722
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Can I analyze my Next Generation Sequencing (NGS) samples on the QIAxcel for Quality control?
FAQ ID - 3724
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How long does an Investigator Quantiplex Pro run take?
FAQ ID - 3727
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Can I buy the 1 ml Bead Plates from the DNeasy UltraClean 96 Microbial Kit (384) separately?
FAQ ID - 3726
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Is an additional proteinase K digest possible with DNeasy PowerSoil Kit and DNeasy PowerLyzer Kit?
FAQ ID - 3725
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On which real-time cyclers is the Investigator Quantiplex Pro Kit validated?
FAQ ID - 3728
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Can the Investigator Quantiplex Pro Kit be run on on the Rotor-Gene Q?
FAQ ID - 3729
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Which real-time cycler software version can be used to run the Investigator Quantiplex Pro Kit?
FAQ ID - 3730
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Do I have to calibrate new dyes on my Applied Biosystems 7500 or 7500 Fast Real-Time PCR System?
FAQ ID - 3732
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How long can I store the dilutions of the Male Control DNA M1 standards at 8°C?
FAQ ID - 3733
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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
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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
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Which human target is used for the quantification?
FAQ ID - 3736
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How long are the target sequences of Investigator Quantiplex Pro?
FAQ ID - 3735
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At what temperature should I store the Investigator Quantiplex Pro Kit?
FAQ ID - 3737
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How can I streamline the quantification workflow?
FAQ ID - 3738
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Does QIAGEN offer an anti-GFP gapmer control?
FAQ ID - 3739
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How long does an Investigator Quantiplex Pro RGQ run take?
FAQ ID - 3740
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On which real-time cyclers is the Investigator Quantiplex PRO RGQ Kit validated?
FAQ ID - 3741
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Which Rotor-Gene Q System can be used to run the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3742
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Which real-time cycler software version can be used to run the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3743
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How long can I store the dilutions of the Male Control DNA M1 standards at 2–8°C?
FAQ ID - 3744
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How long are the target sequences of the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3746
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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
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Which human target is used for the quantification?
FAQ ID - 3747
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At what temperature should I store the Investigator Quantiplex Pro RGQ Kit?
FAQ ID - 3748
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How can I streamline the quantification workflow?
FAQ ID - 3749
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Which fixation method is used in the PAXgene Tissue System?
FAQ ID - 3600
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What is the fixation reagent of PAXgene Tissue FIX?
FAQ ID - 3601
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What is the stabilization reagent of PAXgene Tissue STABILIZER?
FAQ ID - 3602
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What is the maximum tissue size that can be fixed in a PAXgene Tissue FIX Container (50 ml)?
FAQ ID - 3604
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Why are two reagents used in the PAXgene Tissue System?
FAQ ID - 3603
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Which conditions are recommended for the storage of tissues in PAXgene Tissue STABILIZER?
FAQ ID - 3605
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Is it possible to process formalin-fixed and PAXgene Tissue fixed samples together in one run?
FAQ ID - 3606
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Is it necessary to clean a processor normally used for formalin-fixed tissue before using it with PAXgene Tissue fixed tissue?
FAQ ID - 3607
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Is it possible to integrate the PAXgene Tissue STABILIZER into tissue processing?
FAQ ID - 3608
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Are immunohistochemistry (IHC) assays developed for formalin-fixed, paraffin-embedded (FFPE) tissues compatible with PAXgene Tissue fixed, paraffin-embedded (PFPE) tissues?
FAQ ID - 3609
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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
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How well is RNA integrity preserved in PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3611
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How well is DNA integrity preserved in PAXgene Tissue fixed, paraffin-embedded (PFPE) tissue?
FAQ ID - 3612
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Are special kits and protocols required to isolate biomolecules from PAXgene Tissue fixed, cryo-embedded (PFCE) tissue?
FAQ ID - 3614
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What are the yield and integrity of nucleic acids isolated from blocks of PAXgene Tissue fixed, cryo-embedded (PFCE) tissue?
FAQ ID - 3613
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Does the PAXgene Tissue RNA Kit co-purify small RNAs?
FAQ ID - 3615
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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
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Can proteins be extracted from PAXgene Tissue fixed specimens?
FAQ ID - 3616
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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
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How is the quality of proteins purified from PAXgene Tissue fixed and stabilized tissue?
FAQ ID - 3619
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How do I prepare Buffer MP?
FAQ ID - 3620
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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
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Can the RNeasy kits be used to extract RNA from saliva collected using the Oragene collection kit?
FAQ ID - 3623
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How do I analyze codon 61 mutations with the RAS extension kit (cat. no. 971590)?
FAQ ID - 3622
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Are the QIAshredder columns included in various QIAGEN kits the same?
FAQ ID - 3624
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Do I need to use a blood collection set with the PAXgene Blood ccfDNA Tube?
FAQ ID - 3626
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Are QR codes recognized by QIAsymphony?
FAQ ID - 3625
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Does the insert sequence provided in the specification sheet correspond to the target sequence or to anti-sense sequence?
FAQ ID - 3627
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What is the reagent in the PAXgene Blood ccfDNA Tube?
FAQ ID - 3632
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What is the shelf life of unused PAXgene Blood ccfDNA Tubes?
FAQ ID - 3633
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How should unused PAXgene Blood ccfDNA Tubes be stored?
FAQ ID - 3634
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Are PAXgene Blood ccfDNA Tubes sterile?
FAQ ID - 3636
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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
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What is the expected ccfDNA yield from plasma generated from 10 ml of blood?
FAQ ID - 3637
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How long can whole blood stabilized in PAXgene Blood ccfDNA Tubes be stored at room temperature?
FAQ ID - 3639
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Can I use plasma from underfilled PAXgene Blood ccfDNA Tubes?
FAQ ID - 3638
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Can whole blood in PAXgene Blood ccfDNA Tubes be stored at temperatures below 15°C?
FAQ ID - 3641
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Can whole blood in PAXgene Blood ccfDNA Tubes be stored at temperatures above 25°C?
FAQ ID - 3640
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Can whole blood be frozen in PAXgene Blood ccfDNA Tubes?
FAQ ID - 3642
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How long and at which temperature can plasma generated from whole blood in PAXgene Blood ccfDNA Tubes be stored?
FAQ ID - 3644
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Is double centrifugation required for plasma processing?
FAQ ID - 3643
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How should I thaw frozen plasma samples?
FAQ ID - 3645
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What should I do if cryoprecipitates form while thawing a frozen plasma sample?
FAQ ID - 3646
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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
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Which plasma volumes can I process with the QIAsymphony PAXgene Blood ccfDNA protocols?
FAQ ID - 3648
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How long after first use can a reagent cartridge be stored for further use?
FAQ ID - 3650
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For what type of sample material is the QIAsymphony PAXgene Blood ccfDNA Kit intended?
FAQ ID - 3652
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Which tubes are recommended for the QIAsymphony sample rack
FAQ ID - 3653
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Which protocol line should I use to process plasma samples?
FAQ ID - 3654
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How should eluates produced with the PAXgene Blood ccfDNA System be stored?
FAQ ID - 3657
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Does the QIAsymphony PAXgene Blood ccfDNA Kit also allow eluting ccfDNA in less than 60 µl?
FAQ ID - 3656
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Which downstream applications have been tested with ccfDNA purified from whole blood collected and processed with the PAXgene Blood ccfDNA System?
FAQ ID - 3658
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What is the shelf life of the QIAsymphony PAXgene Blood ccfDNA Kit?
FAQ ID - 3651
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Which elution volumes are available with the QIAsymphony PAXgene Blood ccfDNA Kit?
FAQ ID - 3655
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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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