Designing PCR Primers for Restriction Enzyme-mediated Cloning

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  • Опубликовано: 6 окт 2024
  • How to design primers that will amplify a promoter from the human genome, which you can then clone into an expression plasmid using restriction enzymes and a DNA ligase.
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Комментарии • 9

  • @danieltito1234
    @danieltito1234 3 года назад +16

    Ok man your video was cool, but i was expecting more about primer design for restriction sites.
    I came up on this video looking for the difference between linkers and Oligos designed to add restriction sites of our interest's insert, and to be honest i didn't find it in your video. Good quality tough. Regards

  • @cacevedo07
    @cacevedo07 2 года назад

    This Man should have a million subscribers!
    Many thanks for your videos.

  • @adwoabiotech
    @adwoabiotech 4 года назад +2

    Exceptional walk through - thank you⭐⭐⭐⭐⭐

  • @nadaj.9943
    @nadaj.9943 4 года назад +3

    That was really helpful, thanks!!

  • @Milo-tl9oq
    @Milo-tl9oq 2 года назад

    you are awesome. Thanks for your time!

  • @elissaalam6724
    @elissaalam6724 4 года назад +2

    That was great, thanks!

  • @lolohsn2515
    @lolohsn2515 2 года назад +1

    Good video Dr. elmer ! but how did we design primers with R.E sites for new promotor

  • @aryarezayi8622
    @aryarezayi8622 10 месяцев назад

    Thank you ❤

  • @rahelehroudi7379
    @rahelehroudi7379 3 года назад

    My aim is to replace the EF1-A promoter in the pT3-EF1α plasmid with CLEC4F promoter. Please guide me in this regard.