Jump to content

KubaK

New Members
  • Posts

    1
  • Joined

  • Last visited

Posts posted by KubaK

  1. Hello!

    I need a bit of help with my Msc research. I've identified a mutation that I want to check in zebrafish. Workflow is:

    1. RNA isolation and reverse transcription (oligo(dT) primers)

    2. Here i have a problem. I want to tag those genes with HA-tag, but i dont know how to design primers valid for cDNA amplification. How to amplify this correct strand of cDNA i want to check?

    3. Put it in a pCS2+ plasmid.

    4. Mutagenesis of a specific nucleotide.

    5. Put it into the bacteria, isolation and shooting into the zebrafish embryo.

    How do I design those primers specific for cDNA? Is there any spoecific way, or just normally as in regular genomic PCR? Also during reverse transcription should I use oligo(dT) and random hexamers mixture?

×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.