Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • yog77
    Member
    • Jun 2011
    • 18

    #1

    Fluidigm PCR amplicon Library prep

    Hi has any one got any advice on a two-step PCR amplicon library generation via barcode/adapter addition using a secondary PCR.

    I am using the Fluidigm AA system have generated my Primary PCR amplicons 48 samples each with 48 amplocons and now need to attach the barcode/adapter via a secondary PCR. Fluidigm suggest using a 1in100 dilution of the primary PCR and adding the adapters using 15 cycles in a 20uL PCR.

    My question is would it not be better to use a less dilute amount of the primary PCR say 1in20 or 1in40 dilution and cut the number of cycles to 12 or 13 and even in half the reaction volume (say 10uL), therefore reducing PCR errors by using fewer additional cycles? I just wondered if these modifications would be beneficial?

    Thanks
  • ugm6hr
    Junior Member
    • Feb 2011
    • 4

    #2
    Originally posted by yog77 View Post
    Hi has any one got any advice on a two-step PCR amplicon library generation via barcode/adapter addition using a secondary PCR.

    I am using the Fluidigm AA system have generated my Primary PCR amplicons 48 samples each with 48 amplocons and now need to attach the barcode/adapter via a secondary PCR. Fluidigm suggest using a 1in100 dilution of the primary PCR and adding the adapters using 15 cycles in a 20uL PCR.

    My question is would it not be better to use a less dilute amount of the primary PCR say 1in20 or 1in40 dilution and cut the number of cycles to 12 or 13 and even in half the reaction volume (say 10uL), therefore reducing PCR errors by using fewer additional cycles? I just wondered if these modifications would be beneficial?

    Thanks
    This makes perfect sense, but I didn't want to deviate from their published protocols for my experiment.
    If you do use an alternate dilution / number of PCR cycles, I'd be interested to hear the outcome.

    Comment

    • yog77
      Member
      • Jun 2011
      • 18

      #3
      After trying a few different dilutions and cycle combinations and checking them on the bioanalyzer. I went with the following:

      1uL of the primary PCR product as template for a 5uL secondary/barcoding PCR with only 8 cycles. This worked very well and gave good sequencing results. If you require further details let me know.

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
        by SEQadmin2



        CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

        Despite this, “CRISPR helped turn genome editing from a specialized technique into
        ...
        Today, 11:01 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        07-20-2026, 11:48 AM
      • SEQadmin2
        Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
        by SEQadmin2



        Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
        ...
        07-09-2026, 11:10 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Today, 02:55 AM
      0 responses
      8 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-23-2026, 11:41 AM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-20-2026, 11:10 AM
      0 responses
      24 views
      0 reactions
      Last Post SEQadmin2  
      Working...