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  • Akira
    Member
    • Sep 2010
    • 16

    #1

    Validation of Custom Sequencing Primer

    Hi.

    I would like to use my own sequencing primer. I design it with properties (Tm
    and GC content and length etc) close to standard Illumina Sequencing Primer.

    To check its performance I set up a PCR reaction with the primer as forward and P7 primer as reverse. But I don't know what is the annealing temperature I should use.

    Anyone know what is the temperature for Illumina Sequencing Primer to anneal during cBOT last step (not sure if it's correct)? So that I can follow the temperature in my PCR step to see if my primer can anneal.

    Please help. Thanks

    - NGS newbie.
  • giampe
    Member
    • Aug 2009
    • 23

    #2
    Hi,
    maybe if you take a look into http://molbiol.ru/wiki/Cluster_generation_on_cBot
    probably it will help to answer your question.

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