Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • anjama
    Member
    • Mar 2016
    • 15

    #1

    CTAB alternative for carboxyl mag bead gDNA extraction

    Last summer I developed a protocol for our lab to extract gDNA from tissue samples using the carboxyl coated magnetic beads used in SPRI. It has worked really well with a lot of advantages including increased throughput, reduced cost, and very clean samples. Cell lysis is performed in a Tris, EDTA, NaCl, SDS solution with Pro-K, which is then mixed directly with the PEG and NaCl bead solution.

    Now I'm trying to modify it for another project to extract DNA from epithelial cells in fecal samples of herbivores. As is, the protocol does appear to successfully extract DNA, but the quality is terrible and doesn't seem to work in a PCR. Presumably, there are polysaccharides and phenols carrying over in the process from the plant material in the fecal sample, which could explain the poor quality scores and failed PCRs.

    My next step was to introduce an extra step after the intial bead extraction where I place the beads in a 2% CTAB lysis (with Polyvinylpyrrolidone, aka PVP) solution to try and remove the saccharides and phenols. I did this step separately from the initial lysis because it's my understanding that the SDS (anionic) and CTAB (cationic) could precipitate out with each other. However, I'm finding that mixing the beads with the CTAB is causing the beads to clump up and float. My guess is that the relatively negative charge of the beads is causing them to form micelles with the cationic CTAB.

    Are there any suggestions to keep this from happening? Or an alternative to CTAB for removing polysaccharides that is bead friendly?
  • austinso
    Member
    • Jun 2012
    • 77

    #2
    Yes...that would be expected...can't really avoid it either...it depends on the coating on the bead (they have slightly different versions).

    So one thing you could do is pellet the nucleic acids (well all negatively charged polymers) in the CTAB solution (I forgot what the w/v concentration should be to do that...and don't know if PVP offsets that) and remove the soup, then resuspend in SDS and then do the bead clean up with that resuspended material.

    But...hard to know without more details...

    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, 10-22-2026, 11:13 AM
    0 responses
    27 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    20 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
    43 views
    0 reactions
    Last Post SEQadmin2  
    Working...