Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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.

  • #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

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin


      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
      Yesterday, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    39 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    41 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    35 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Working...
    X