Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • fangw
    Junior Member
    • Jan 2014
    • 1

    #1

    Fail in ligation of 5' RNA adapter

    Hello,

    I am looking for help with library preparation in MiSeq. I have tried to ligate 5' RNA adapter (33bp) to RNA (22bp) already ligated to 3' DNA adapter (33bp), but it did not show any band at about 88bp. I have tested that the 3' adapter ligation is fine. The concentration of 5' adapter is 5 uM, and my ligation condition is 1h at 20 degree using T4 RNA ligase. I also tried 37 degree and overnight ligation, did not work. This 5' adapter terminates with "U". Will it affect ligation process? Any idea how to solve this problem? Thanks.
  • Genohub
    Registered Vendor
    • Mar 2013
    • 210

    #2
    small rna ligation of 5'adapter

    Sometimes it's difficult to visualize a doubly ligated small rna product (rna with a 3'ligated and 5'ligated adapter). The ligation efficiencies are pretty low, making it difficult to visualize on a gel. I would try running your sample on a bioanalyzer. You could also make a synthetic control RNA (with 5'phosphate and 3'OH) to check your 3 and 5'ligations. You'll be able to see this much better than small RNA isolated from cells or tissue.

    - Genohub

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
      by SEQadmin2



      Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

      Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
      ...
      10-14-2026, 09:55 AM
    • SEQadmin2
      New Genomics Technologies Take Aim at Long-Standing Limits
      by SEQadmin2


      Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

      We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
      ...
      09-28-2026, 10:25 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    14 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    21 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-13-2026, 09:56 AM
    0 responses
    19 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-09-2026, 11:14 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Working...