Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Metagenomic with 454 Junior

    I try to sequence multiplex (21 samples) amplicons for months !! Amplicon size is around 609 pb (with MID ...). The problem is that the yield is very low (2%) with 2 or 4 cpb and when I sequence I juste have 50 bp instead of 609 pb (bioanalyzer is ok, no small fragments).

    Do you think to increase elongation time of emPCR will be better or the problem come from an other step ?

    Thank for your help !

  • #2
    Originally posted by Pascale View Post
    I try to sequence multiplex (21 samples) amplicons for months !! Amplicon size is around 609 pb (with MID ...). The problem is that the yield is very low (2%) with 2 or 4 cpb and when I sequence I juste have 50 bp instead of 609 pb (bioanalyzer is ok, no small fragments).

    Do you think to increase elongation time of emPCR will be better or the problem come from an other step ?

    Thank for your help !
    You are experiencing things that a lot of users are experiencing. Do the following to minimize your losses:

    1) increase your cpb to between 15 and 30cpb. I know this seems insane but it's the only way.
    2) get a KAPA qPCR Lib-A/Lib-L kit to accurately quantify libraries.
    3) ask for newest lots to be shipped to you and hope.

    Comment


    • #3
      You can also try the long amplicon emPCR protocol since yours is >600bp.

      Comment


      • #4
        Thank you very much for your advice ! I will try all of that this afternoom and I will let you know. Have a good day.

        Comment


        • #5
          We size select twice with Ampure XP for amplicon sequencing, primer (and/or primer dimer) that is undetectable by bioanalyzer can still lead to a big short read spike. Our amplicon is 676 bp and the long emPCR protocol had an instant and amazing effect on improving the runs on our Jr.

          Our optimized cbp is 0.35 - so seems very variable from site to site. The kapa kits are expensive, particularly relative to a Jr run, so we don't use them.

          Comment

          Latest Articles

          Collapse

          • 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
          • seqadmin
            Strategies for Sequencing Challenging Samples
            by seqadmin


            Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
            03-22-2024, 06:39 AM

          ad_right_rmr

          Collapse

          News

          Collapse

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