This kit can be used in two modes.  It can be used for isoform discovery or to evaluate transcript adundance.  Running it in the first mode will deliver abundance data as well.  This kit provides a comprehensive survey and accurate relative abundance of every transcript in RNA samples. Single molecule long read data is generated as well as relative abundance using barcode based molecular counting. It also features a multiplex workflow that pools 24 samples into a single tube with less than 3 hours of hands-on time.

It’s the perfect kit for labs looking to profile every transcript in their sample. Compatible with all Illumina instruments.*
 

*HiSeqs, NextSeqs, and NovaSeqs are recommended for per base cost benefits.

 

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User Manual

 

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LoopSeq™ Transcriptome 3x8-plex Kit

$1,699.00Price
  • Free shipping in the United States

  • Assay Time

    8.5 hours

    Hands-On Time 2.5 hours
    Mechanism of Action Synthetic long read sequencing
    Multiplexing Allows for 8 samples to be processed in one tube
    Input Quantity 10ng of total RNA
    Category Transcriptome
    System Compatibility HiSeq 2500, HiSeq 3000, HiSeq 4000, NextSeq, NovaSeq, MiSeq, MiniSeq
    Nucleic Acid Type RNA
    Method 2 x 150 Paired End (PE) sequencing
    Specialized Sample Types Eukaryotic sample
    Technology Assembly of a synthetic long reads form short reads
    Automation Capability Yes

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San Jose, CA 95138 USA
Tel: 650-815-7088
Toll-Free: 844-238-1849
Fax: 650-285-2387
sales@loopgenomics.com
techsupport@loopgenomics.com

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