Комментарии •

  • @sebastiaanbol5778
    @sebastiaanbol5778 5 лет назад +5

    Excellent video (as always). Please note, the blue/white screening only works if your ligation disrupts the LacZ gene in your plasmid. Not all plasmids contain this gene.

  • @anacristinademartinez3495
    @anacristinademartinez3495 Год назад

    ¡GRACIAS!

  • @mrsoup5034
    @mrsoup5034 6 лет назад

    Thank you so much 😄that was really helpful

  • @rakeshchaudhary2246
    @rakeshchaudhary2246 6 лет назад +1

    Here in this video competent cells are added after plates are made...Can we directly put competent cells along with X gal iptg

  • @AmalDhivaharSURBT
    @AmalDhivaharSURBT 6 лет назад

    so good :-)

  • @jmlee2115
    @jmlee2115 9 лет назад +1

    Hi, how do you measure 20mg of x-gal when it is in a solution form?

    • @Goldbio
      @Goldbio 9 лет назад

      +JM Lee Hi JM. You can measure 20mg of X-Gal based on the concentration of the solution. So if your stock solution is 20mg/mL, then you would need 1mL of stock solution to get 20mg of X-Gal. If you needed 40mg of X-gal, you would use 2mL, and so on.

  • @ayeshagul2699
    @ayeshagul2699 6 лет назад

    hello ...
    i am doing transformation nowadays ... but i am unsuccessful can you please guide me ???

  • @raymondvincentcastillo1437
    @raymondvincentcastillo1437 7 лет назад

    can I use Glu Gal instead of X-gal?

  • @joshuacidalvarado1775
    @joshuacidalvarado1775 10 лет назад +4

    He reading.

  • @hermanozenaide19
    @hermanozenaide19 6 лет назад

    Is it really safe to do this at 2:33?

    • @sebastiaanbol5778
      @sebastiaanbol5778 5 лет назад

      Yes, but i never do it. It's not really necessary.

  • @Luphedza
    @Luphedza 2 месяца назад

    Play dno