Plaque Assay for Influenza Virus

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  • Опубликовано: 5 окт 2024
  • ( www.abnova.com ) - The plaque assay is a widely used approach for purifying a clonal population of virus and determining the viral titers (the lowest concentration of virus that results in infection). This video shows the procedure of plaque assay for influenza virus. More videos at Abnova www.abnova.com

Комментарии • 25

  • @fups1
    @fups1 4 года назад +3

    Great music and even better video! thank you!

  • @shanyuxi
    @shanyuxi 4 года назад +4

    always use filtered tips!

  • @ithagag1751
    @ithagag1751 11 лет назад +2

    Very helpful video

  • @middlevoids
    @middlevoids Год назад

    Nice and clear. Thanks!

  • @paulabenitezbolivar5545
    @paulabenitezbolivar5545 6 лет назад +2

    great video! thanks!

  • @melissarobinson9365
    @melissarobinson9365 4 года назад +1

    Great video.

  • @ThuNguyen-jj8de
    @ThuNguyen-jj8de Год назад

    thank you so much

  • @lyvian0321
    @lyvian0321 10 лет назад

    Hi tq so much for this video. Very helpful. Anyway, I wonder where is your source or more precisely how should I cite this method in my paper later?

  • @Sh.zaeemi
    @Sh.zaeemi 10 месяцев назад

    Fantastic

  • @dianindierahmalia2301
    @dianindierahmalia2301 3 года назад

    What is a cell solution? A sample or not?

  • @HO-YTchannel
    @HO-YTchannel 3 года назад +1

    But why 1080 ul and 120 ul and not just 1000 ul and 100 ul ?

    • @maureen2888
      @maureen2888 3 года назад

      I know right? I was wondering the same. Why complicate things

    • @bussayaratmaikhunthod2251
      @bussayaratmaikhunthod2251 3 года назад +5

      Just to make sure you have enough virus solution to infect the cells. In this video they use 500ul for each well and they did 2 rep(wells) per dilution of virus. So if you prepare exactly 1000uL, with the general error of pipetting you surely don't have enough virus stock for 2 wells.

    • @ThuNguyen-jj8de
      @ThuNguyen-jj8de Год назад

      they have 2 plates for the duplicate experiment so they need at least 1000ul virus solution and the dilution ratio should be 10-time dilution so it is 100 virus 900ul (total 1000ul) therefore with their experiment, they want to make sure they have enough virus solution with 1200ul in total

  • @adrianwoodlock8433
    @adrianwoodlock8433 2 года назад

    Can someone help me understand what this experiment is showing

  • @紀博文-i8l
    @紀博文-i8l 4 года назад

    nice

  • @herbeyoswaldo
    @herbeyoswaldo 10 лет назад

    don't you use trypsin to infect?

  • @omaradenis1196
    @omaradenis1196 2 года назад

    I would like to inquire whether the medium mixed with 3% agarose is containing FBS or not.

    • @ThuNguyen-jj8de
      @ThuNguyen-jj8de Год назад

      it not contain FBS but i think it contain TPCK for virus infection

    • @adarshguptak
      @adarshguptak Год назад

      Yes, the growth medium with agar should have FBS. Avoid FBS only in virus dilutions as it may affect cell adsorption.

  • @asoro_1632
    @asoro_1632 3 года назад

    Pozdrowienia z uzetu

  • @kurniawahyu
    @kurniawahyu 11 лет назад

    Is it work with c6/36?
    except for 37。C degree, (c6/36 requiring 27。C instead), all the step would be same?
    I am looking forward to count my virus titer using C6/36
    Thank you

    • @bhuvanroyal5909
      @bhuvanroyal5909 3 года назад

      Could you explain how we get Dilution factor.

    • @UmerAli-lr9ll
      @UmerAli-lr9ll 2 года назад

      Depends on whether your virus is cytolytic on C636 or not. If you want to just do the growth/replication kinetics of your virus on C636, you can use the infected supernatant from C636 at different time points and titrate it on more susceptible cell lines like Vero E6 or CV1 cells. Some arboviruses despite giving good yield from insect lines wont cause much cytopathic effects.Good luck!