Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Bioo Scientific
    Registered Vendor
    • Oct 2009
    • 99

    #1

    RNA-Seq Improved

    Bioo Scientific recently launched the NEXTflex™ Rapid RNA-Seq Kit which offers a fast and flexible library prep solution using as little as 10 ng of mRNA or rRNA depleted total RNA.

    Complete RNA-Seq library prep solution
    The NEXTflex Rapid RNA-Seq Kits provide a simple, cost-effective solution for generating libraries from mRNA or rRNA depleted total RNA that are compatible with Illumina's sequencing platforms.

    Flexible multiplexing options which greatly reduce sequencing costs
    NEXTflex™ Barcodes Kits contain 6, 12, 24, 48 or 96 unique barcodes which contain embedded index sequence.

    Increased number of unique sequencing reads
    "Enhanced Adapter Ligation Technology" allows for ligations with longer adapters and better binding efficiencies.

    Faster gel-free protocol
    By incorporating a completely gel-free, bead-based cleanup, the NEXTflex RNA-Seq Kit reduces the amount of time needed for library preparation

    You can read more about the NEXTflex Rapid RNA-Seq Kit, the NEXTflex RNA-Seq Barcodes and the NEXTflex-96 RNA-Seq Barcodes to see how they can improve your RNA-seq library preps. Like our other library prep kits, the NEXTflex RNA-Seq Kits are all available for next day delivery. These kits have been functionally validated with GAIIx, HiSeq and MiSeq platforms.
    Last edited by Bioo Scientific; 06-03-2014, 11:21 AM.
  • bruce01
    Senior Member
    • Mar 2011
    • 160

    #2
    I would be interested to see comparisons with libraries prepd with Truseq kits, do you have any info? The 96 barcodes is a +, I expect Illumina to release a v3 with that soon so will be down to how they perform. Hence my first question.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Today, 10:35 AM
    0 responses
    6 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    23 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    41 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    47 views
    0 reactions
    Last Post SEQadmin2  
    Working...