Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jlove
    Member
    • Apr 2011
    • 49

    #1

    Assay to test for ligation efficiency?

    Hi,
    Has anyone got a method for assessing TruSeq ligation efficiency, pre-PCR? We use the KAPA Illumina library quant kit for final library quantification, and I can certainly try using this, but I am wondering if anyone knows about actually using the results to assess the efficiency? I'm not sure how to evaluate the results to determine next steps.
    Thanks in advance!
  • jdk787
    josh kinman
    • Apr 2014
    • 72

    #2
    Originally posted by jlove View Post
    Hi,
    Has anyone got a method for assessing TruSeq ligation efficiency, pre-PCR? We use the KAPA Illumina library quant kit for final library quantification, and I can certainly try using this, but I am wondering if anyone knows about actually using the results to assess the efficiency? I'm not sure how to evaluate the results to determine next steps.
    Thanks in advance!
    You could try ligating, then quantifying your sample with Qubit to determine the total amount of DNA present.
    Then quantify the same sample with the KAPA quantification kit which will only measure the amount of ligated material in your sample.
    Ligation efficiency can then be determined by comparing the Qubit number to the Kapa number.
    Josh Kinman

    Comment

    • HESmith
      Senior Member
      • Oct 2009
      • 512

      #3
      Be aware that the KAPA assay will detect adapter dimers as well as bona fide library clones. While dimers are the product of ligation, I suspect that's not what you want to measure :-).

      The TruSeq kit contains inline controls for the enzymatic steps, including ligation, so you may want to incorporate those into your protocol.

      Comment

      • RNA_
        Junior Member
        • Nov 2015
        • 8

        #4
        If your lab is licensed for radioactive work, prepare a test library in parallel using trace amounts of 32P-labeled substrate spiked into your sample --> run on PAGE with appropriate radiolabeled size markers --> phosphorimaging.

        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, Yesterday, 11:13 AM
        0 responses
        17 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        18 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        36 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        42 views
        0 reactions
        Last Post SEQadmin2  
        Working...