Microbiology: The spread plate technique

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  • Опубликовано: 5 июл 2024
  • Learn how to make a glass spreader and aseptically spread an aliquot of bacteria evenly onto the surface of an agar plate.

Комментарии • 24

  • @MrWhangdoodles
    @MrWhangdoodles 26 дней назад

    Excellent video.

  • @Mayanfull
    @Mayanfull 3 года назад +3

    Thanks!! I needed a reminder and this was very useful!

  • @farahali463
    @farahali463 3 года назад

    u r so good, thank u bc of u I'll take a very good score in the exam

  • @MrMRbarati
    @MrMRbarati 9 месяцев назад

    Thanks a lot David. I am planning to do this experiment in our lab for the first time. Your demonstration made me feel confident. Cheers

  • @sawairagul251
    @sawairagul251 3 года назад +1

    Well explained 👌🏼

  • @user-wk2gp3tu8h
    @user-wk2gp3tu8h 2 года назад +1

    Thank you 💯💯

  • @alisaleh1987
    @alisaleh1987 2 года назад

    thank you s🇮🇶Thank you, sir. I am from Iraq, and this lesson we have is in biology Thank you very much

  • @byronmunashe3827
    @byronmunashe3827 2 года назад

    Well explain.👍👍👍👍👍

  • @vet.doctoraliakbarrehmat2914
    @vet.doctoraliakbarrehmat2914 3 года назад

    Thanks

  • @arunkalaivanan8075
    @arunkalaivanan8075 Год назад

    sir, i have doubt, about why there is moisture alone with the bacterial colony in the end pic?

  • @haroldosoares6531
    @haroldosoares6531 2 года назад

    muito bom, perfeito 👍

  • @lauryngrcic6237
    @lauryngrcic6237 2 года назад

    What about the very small amount of inoculum that is inevitably left on the spreader tool? Doesn't that loss of volume affect your CFU calculation if the true volume isn't delivered to the plate? Why doesn't the loss of volume matter?

    • @davecummings6328
      @davecummings6328  2 года назад +4

      Hi Lauryn. You could try to calculate how much is lost based on surface area of the spreader and surface tension of the broth. But my guess is that it's a few uL and the change in colony count is probably well within the error of the technique anyway. All that is to say that I don't think it would impact your results significantly.

  • @vetberrypk
    @vetberrypk 3 года назад +1

    What should be the temperature inside incubator ?

    • @josephgaleno5098
      @josephgaleno5098 2 года назад +2

      Little late but typically E.coli on petridish can grow at 35c. At this temperature, you should be able to see growth within 24 hours.

    • @davecummings6328
      @davecummings6328  2 года назад

      usually 37C, but that depends on the species of bacteria.

    • @sushamapawar5842
      @sushamapawar5842 Год назад

      I also watch your vidios pleas give a way after dmlt diploma in medical lab tech. Need your guidance sir

    • @sushamapawar5842
      @sushamapawar5842 Год назад

      I also watch your vidios pleas give a way after dmlt diploma in medical lab tech. Need your guidance sir

  • @sarekaya4815
    @sarekaya4815 Год назад

    I tried this method, but the bacteria did not grow as colonies, they grew in the whole plate and I could not count the colonies. What is the reason? thanks

    • @fukyoutubestupidfuckinghandles
      @fukyoutubestupidfuckinghandles Год назад

      This method covered the whole plate so that's how it grew. This method isn't for counting colonies.

    • @fukyoutubestupidfuckinghandles
      @fukyoutubestupidfuckinghandles Год назад +1

      streak plate method might be better but ive just started so there's probably a better method i dont know

    • @ashlykraphy9933
      @ashlykraphy9933 Год назад

      Sare kaya, You probably need to dilute the sample more so that you get it in countable range which is 20-200 for spread plating technique.

  • @pabasarasamarawickrama8404
    @pabasarasamarawickrama8404 Год назад

    Oo😂❤❤o❤oo❤❤❤o❤o❤ oki iiooi❤❤❤k😊kk