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  2. ProdDescription

ProdDescription

414 Articles
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Target gene expression levels are often normalized to the expression of a “housekeeping gene” (reference gene) to correct for differences in the amount of input RNA and variations in reaction efficiency. How do I select a suitable housekeeping gene?

  • 528
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How can amplification of genomic DNA in total RNA samples be avoided?

  • 493
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What are the benefits and application of two-step RT-qPCR?

  • 578
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What are the benefits and application of one-step RT-qPCR?

  • 510
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Can I purchase RCU buffer from 740910 NucleoSpin RNA Clean-up Maxi?

  • 416
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What is Marcherey Nagel Carrier RNA made of?

  • 411
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What are the sizes of holes of the NucleoBond Smart Rack?

  • 464
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What are the differences between 744950 (KingFisher 96 Accessory Kit A) and 744951 (KingFisher 96 Accessory Kit)?

  • 477
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Can samples lysed in TriZol be used on the NucleoSpin® RNA Set for NucleoZOL™?

  • 433
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What are the dimensions of the NucleoSpin® 96 Plasmid Filter Plates?

  • 485
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What are the dimensions of the NucleoVac™ 96 Vacuum Manifold?

  • 504
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Can the NucleoSpin Plasmid Purification columns substitute the NucleoSpin Plasmid Transfection- grade columns to isolate Endo-free plasmid DNA?

  • 354
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What is the number of maximal theoretical UMI combinations in the sequencing reads generated by the SMARTer® Stranded Total RNA-Seq Kit v3 - Pico Input Mammalian?

  • 375
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What is the nature of Unique Molecular Identifiers (UMI) incoporated into the SMARTer® Stranded Total RNA-Seq Kit v3 - Pico libraries?

  • 339
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Can I use a software other than Cogent NGS Analysis Pipeline for the analysis of the sequencing reads generated by the SMARTer® Stranded Total RNA-Seq Kit v3 - Pico Input Mammalian?

  • 335
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What software should I use for the analysis of the sequencing reads generated by the SMARTer® Stranded Total RNA-Seq Kit v3 - Pico Input Mammalian?

  • 583
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What is the advantage of incoporation of Unique Molecular Identifiers (UMI)?

  • 320
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What is the advantage of using Unique Dual Indexes ?

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