MAY 11, 2017 12:00 PM PDT
New multiplexed nCounter® PlexSet™ Reagents- an alternative to qPCR technology
Presented at the Genetics and Genomics 2017 Virtual Event
SPONSORED BY: Nanostring Technologies
CONTINUING EDUCATION (CME/CE/CEU) CREDITS: P.A.C.E. CE | Florida CE
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Speakers:
  • the Molecular Biology Core Facility Manager, Geisel School of Medicine at Dartmouth
    Biography
      Christian H. Lytle is the Molecular Biology Core Facility Manager at Geisel School of Medicine at Dartmouth. He has more than 30 years of research experience in various roles and is affiliated with societies such as The Association of Bimolecular Resource Facilities (ABRF). He has received many awards and recognitions for his work in the genomics field.

    Abstract:

    The nCounter® Analysis System from NanoString® Technologies uses a novel molecular barcoding technology to measure multiplexed gene expression of up to 800 targets with simple, enzyme- free, direct probe hybridization and tabulates fluorescent barcodes to provide specific and precise digital data. The standard nCounter gene expression assay includes 12 samples per run. Here we present data from the newly released nCounter PlexSet™ assay which enables researchers to quickly evaluate up to 24 multiplexed targets directly from cell lysates for 96 samples per run. PlexSet Reagents are universal and can be combined with gene-specific probe oligos to digitally quantify any 24 targets directly from cell lysates and total purified RNA from FFPE samples.

     

    The direct digital quantification (no enzymes or amplification), lyse-and-go capability, technical assay controls, high sensitivity, and simple data analysis make this an ideal alternative to standard qRT-PCR. We will report on our experience using this technology, and why we believe it could easily replace many of the qRT-PCR assays being conducted.


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