PCR Troubleshooting: Explanations and How to Fix Common PCR Problems

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  • Опубликовано: 6 окт 2024
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Комментарии • 31

  • @Abdulaziz_9922
    @Abdulaziz_9922 4 года назад +5

    I can't find a good way to thank you ☺️ you saved my life seriously I have to do a prasentation and really just know few about trouble shooting.
    Thaaaank you so much

  • @angelicacastillogarcia6153
    @angelicacastillogarcia6153 2 года назад +2

    I´m really thankful for this amazing video, it was very educative and helped me a lot to discuss the results of the PCR with my classmates. Good job

  • @originalAtreyu
    @originalAtreyu 5 лет назад +1

    Good job. I've been in the business for over ten years and still learned a thing or two.

  • @sandraerdmann6003
    @sandraerdmann6003 11 месяцев назад

    Great video. I just have on comment on negative controls. What you've meant is a no-template control. A negative control contains DNA that is the "wrong" template for your primers, for example from a different species, that doesn't contain that target gene region.

  • @shrutigaggar22
    @shrutigaggar22 3 года назад +1

    This was very informative and I learned a lot.

  • @reyhaneesmaieli1117
    @reyhaneesmaieli1117 4 месяца назад

    this was soooo helpful. thank you

  • @stephaniemurray3771
    @stephaniemurray3771 4 года назад +1

    Super quick and helpful! Thanks!

  • @umisyafiqah8054
    @umisyafiqah8054 2 года назад

    This was really helpful, thanks a lot !

  • @samarakadhim288
    @samarakadhim288 2 года назад

    Very informative and helpful video alot of thanks 🌹🌹🌹

  • @egs8545
    @egs8545 4 года назад

    Thank you for making this video, very helpful!!

  • @wiktoriac8308
    @wiktoriac8308 4 года назад +1

    That was very helpful, thank you!

    • @Goldbio
      @Goldbio  4 года назад

      Glad it was helpful!

  • @Alizaidi-h9p
    @Alizaidi-h9p Год назад

    Good job madam ❤ thank you

  • @Hozanaa
    @Hozanaa 3 года назад

    It's very well explained. ❤️

  • @TheOn3LeftBehind
    @TheOn3LeftBehind 4 года назад

    This was extremely helpful!

    • @Goldbio
      @Goldbio  4 года назад

      Glad it was helpful!

  • @reza310
    @reza310 Год назад

    Very helpful thank you.

  • @hebaomar3001
    @hebaomar3001 Год назад

    Thank you 🙏

  • @NurulHikmawati
    @NurulHikmawati 3 года назад

    You're great teacher. But, my question is when problem no 1, solution is reduce primer. What do you mean that receipt mix or dilution primer that have to turn down?

  • @sydneyschoen96
    @sydneyschoen96 2 года назад

    awesome! thanks!

  • @rhodaking6558
    @rhodaking6558 3 года назад

    thank you so much

  • @malikwaseem7043
    @malikwaseem7043 3 года назад

    Thank you mam.....❤❤❤❤

  • @EelasMusic
    @EelasMusic 3 года назад

    I have the protocols for normal PCR.how can I optimize them for using multiplex PCR

  • @mtha7796
    @mtha7796 4 года назад

    @2.50 what agarose gel electrophoresis conditions that you used? Thank you so much.

  • @preciousayawei4695
    @preciousayawei4695 2 года назад

    Please what do you mean by re-isolate template DNA?

  • @sadianadeem3952
    @sadianadeem3952 3 года назад

    Good

  • @heloisamonteirodoamaralpra9300
    @heloisamonteirodoamaralpra9300 3 года назад

    Trank you!!!!!

  • @Alizaidi-h9p
    @Alizaidi-h9p Год назад

    Good job madam ❤ thank you

  • @noman12310
    @noman12310 4 года назад

    Thank you so much

    • @Goldbio
      @Goldbio  4 года назад

      You're most welcome