Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • emarsola10
    Junior Member
    • May 2016
    • 2

    #1

    Pippin-Prep - External or Internal markers?

    Hi Seqanswers community,

    I going to test size selection step in Pippin-Prep and I´m not sure about the advantages and disadvantages to use the external or internal markers.

    I going to use a 2% dye-free Pippin-Prep cassete gel to select two different ranges, 200-250 and 400-450 bp. The marker options for my experiment are Marker L (internal standards) or Marker K (external standards).

    I have already performed a test using the external Marker K to select the above mentioned ranges and using the 'Range Program Mode'. However, the product size recovered was smaller than selected (around 150 bp for the 200-250 range and around 350 for the range 400-450). I guess if I use a internal instead external marker I can improve accuracy, but I afraid that I can collect a marker fragment togheter with the recovered product.

    Thank you.
  • kmcarr
    Senior Member
    • May 2008
    • 1181

    #2
    Originally posted by emarsola10 View Post
    Hi Seqanswers community,

    I going to test size selection step in Pippin-Prep and I´m not sure about the advantages and disadvantages to use the external or internal markers.

    I going to use a 2% dye-free Pippin-Prep cassete gel to select two different ranges, 200-250 and 400-450 bp. The marker options for my experiment are Marker L (internal standards) or Marker K (external standards).

    I have already performed a test using the external Marker K to select the above mentioned ranges and using the 'Range Program Mode'. However, the product size recovered was smaller than selected (around 150 bp for the 200-250 range and around 350 for the range 400-450). I guess if I use a internal instead external marker I can improve accuracy, but I afraid that I can collect a marker fragment togheter with the recovered product.

    Thank you.
    I have used the Blue Pippin to isolate fragments in the 175-250bp range using Dye-Free cassette BDF2010 (2%) with internal standard V1 and it has worked very reliably. The internal standards are very small so they do not co-migrate with your 200bp fragments.

    You said you tested using Marker K as an external standard. Looking at the Pippin Cassette Reference Chart it lists Marker K as an internal standard meant for the 1.5% cassette. The external standard designated for 2% cassettes is Marker E. That may explain the discrepancy in the fragment sizes recovered.

    Comment

    • luc
      Senior Member
      • Dec 2010
      • 469

      #3
      The internal standards have shorter fragment lengths; they will not be eluted with your sample. With internal standards you can run 5 samples per cassette. We have not noticed any principal differences in accuracy.

      Comment

      • emarsola10
        Junior Member
        • May 2016
        • 2

        #4
        Pippin-Prep - External or Internal markers?

        Thank you for reply.
        I used the external marker E (CEF 2010) and not K, as I said before.

        I think that people from SAGE assistance has found the problem. Checking the log files of our run they found a hump in the curves of the current profile for all lanes, whereas the expected curve must be flat. They gave the following tip: "This ‘hump’ typically indicates that the input sample contains excess salt (>80mM ionic strength). High salt causes an altered migration, and can cause inaccurate sizing. I would suggest performing a purification step to remove excess salt before loading future samples on the Pippin Prep.". This makes sense because we entered with a concentrate PCR product in the gel.

        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
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        15 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        35 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...