Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Koncarius
    Junior Member
    • Jul 2015
    • 2

    #1

    Possibility to run DNA/RNA duplexes on bioanalyzer

    Hello forumers,
    I am currently trying to find out if it's possible to run a bioanalyzer (Agilent 2100) on samples containing DNA/RNA duplexes.

    So I have performed a cDNA synthesis on some rRNA and now I want to measure the size of the cDNA/rRNA hybrid fragments. I guess if I would use the RNA kit it would be impossible to distinguish free rRNA in my sample from the DNA/RNA fragments, but what if I use a DNA kit? I shouldn't have any DNA before the cDNA synthesis so in theory that should give me some information about the DNA/RNA hybrids right?

    Or do you think I should do a second strand synthesis of my DNA/RNA (get rid of the RNA and replace with DNA) in order to get dsDNA and then use a DNA kit for analyzing?
    I'm not very familiar with the exact chemistry behind the dyes of the different bioanalyzer kits and I had a hard time to find this information on the web.

    Thank you in advance
    /Koncarius
  • kerplunk412
    Senior Member
    • Jun 2012
    • 119

    #2
    I would recommend doing the second strand synthesis, purifying, and measuring that product on a DNA chip. Even if the DNA/RNA hybrid shows up on the DNA chip it might not run at the expected size, and I think having a bunch or residual RNA may make the chip run weird or the data difficult to interpret, even on a DNA chip. Also, if your eventual goal is library prep it makes more sense to check the double-stranded cDNA, as this will be the inserts in your library.

    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, Yesterday, 10:35 AM
    0 responses
    9 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    46 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    48 views
    0 reactions
    Last Post SEQadmin2  
    Working...