Serial Dilution and Plate Counts

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  • Опубликовано: 15 окт 2012
  • For more information, visit www.bio-rad.com/yt/7/biotech-l....
    This video demonstrates how to quantitate bacteria using the serial dilution and plate count method. Bacteria are serially diluted and plated onto petri plates using aseptic technique. This activity is included in the laboratory textbook Biotechnology: A Laboratory Skills Course.
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Комментарии • 44

  • @LSI_MGA
    @LSI_MGA 11 лет назад +29

    can you add a video that explains what do you do afterwards? how to analyze the plates?

  • @IdontCareDontReply
    @IdontCareDontReply 11 лет назад +12

    You count the colonies that form in the plate, that is why it is called plate count. With the colonies found on the plate you calculate the CFU (colony forming unit) and have an estimate of viable cells available per mL from your original sample.

  • @IsabelRodriguez-nv2ue
    @IsabelRodriguez-nv2ue 4 года назад

    Thank you so much for this video. It is very clear and easy to follow and understand.

  • @memorya1972
    @memorya1972 8 лет назад +8

    now i know what will i do to my bacteria. thanks for the info :) very well explained.

  • @leonardomelo4673
    @leonardomelo4673 10 лет назад +58

    They really like the color green.

    • @Allysiaj2085
      @Allysiaj2085 3 года назад

      Ghtvgbbt

    • @Paganforge
      @Paganforge 3 года назад

      Right down to the roof of the R&D complex in Hercules, CA.
      www.google.ca/maps/@38.0255571,-122.2766188,3a,75y,323.16h,87.15t/data=!3m7!1e1!3m5!1sZ7M37LTwRXIynelM8B9yag!2e0!6s%2F%2Fgeo1.ggpht.com%2Fcbk%3Fpanoid%3DZ7M37LTwRXIynelM8B9yag%26output%3Dthumbnail%26cb_client%3Dmaps_sv.tactile.gps%26thumb%3D2%26w%3D203%26h%3D100%26yaw%3D70.26178%26pitch%3D0%26thumbfov%3D100!7i16384!8i8192?hl=en

  • @sleeplessbird
    @sleeplessbird 10 лет назад +1

    Nice explanation, thanks for the video.

  • @bukolajoshua8054
    @bukolajoshua8054 8 лет назад +3

    thanks for the explanation

  • @ahmadtalsaadi
    @ahmadtalsaadi 11 лет назад +7

    Dear Bio Rad
    Thank you for this videos, is it possible to upload let say part 2 video to this one showing who to count the plates after incubation? However some people describe below who to count the plate, I do appreciated, but it will be more complete to add plate colonies counts video to this one!
    many thanx to all

  • @miraedo92
    @miraedo92 11 лет назад +1

    thanks for making & uploading such a good video.It's really help in understanding of rDNA Technology subject. I'm having an exam soon.

  • @oparaeberechi980
    @oparaeberechi980 11 лет назад +2

    Thank you for uploading the video is quite educative.

  • @vetaya4783
    @vetaya4783 5 лет назад +1

    Very informative , Thank you

  • @sclair10
    @sclair10 10 лет назад +4

    thank you, I need a refresher and your videos have helped enormously.

  • @TayyabAli-xm2oi
    @TayyabAli-xm2oi 4 года назад

    Well explained!

  • @WorthlessWinner
    @WorthlessWinner 11 лет назад +4

    You count the number of colonies that grow there; that gives an estimation of the number of bacteria in the volume of liquid you inoculated the plate with.
    To get the number of bacteria in 1 ml, you need to account for the volume you put on the plate and the dilution. If you put 0.1 ml on the plate, you need to times that by 10 to get it in ml. If you were counting 10^-5 dilution, you need to times it by 10^5 to get it in 10^1. Cancel those out and you have Colony forming units / ml.

  • @aanagul8787
    @aanagul8787 8 лет назад +2

    thank you

  • @lorenaviernes6269
    @lorenaviernes6269 6 лет назад +1

    hello! this video is very usefull..:) and it helps me so much for my upcoming research. can i ask.. what can i substitute to lb agar?

  • @ItsSunnySara
    @ItsSunnySara 2 года назад +1

    how long should u wait for cooling down?

  • @innestri807
    @innestri807 3 года назад

    Nice video 👍🏻

  • @thesensiblecoderguy
    @thesensiblecoderguy 10 лет назад +1

    very well explained

  • @codyellsworth7927
    @codyellsworth7927 3 года назад

    Totally rad-ical

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

    Thank you sir

  • @a.s9509
    @a.s9509 Месяц назад

    Do you discard 100 microliters from the last (7th) microtube?

  • @joelarnaud6023
    @joelarnaud6023 2 года назад +2

    This way of dilutions are not supposed to be 10 minus 1, 10 minus 2, 10 minus 3 etc?

    • @ssaha7776
      @ssaha7776 4 месяца назад

      They are -1 -2- 3

  • @Hira_Hyuna
    @Hira_Hyuna 4 года назад +2

    Subtitle please.

  • @omarito1991
    @omarito1991 10 лет назад +17

    more of this videos on youtube and less justin bieber videos please :) thanks

  • @NileshRoamingNITIAN
    @NileshRoamingNITIAN 3 года назад

    When you love greenery more than anyone !!

  • @VLogKeluargaArsyla
    @VLogKeluargaArsyla 3 года назад +1

    Alhamdulillah hadir

  • @JYOtiRaNJanMANgaRaj
    @JYOtiRaNJanMANgaRaj 4 месяца назад

    ❤❤❤❤❤❤

  • @mohitmahajan4021
    @mohitmahajan4021 7 лет назад +2

    there is no plaque counting in this video

  • @emmylouhaught8572
    @emmylouhaught8572 3 года назад

    It didn't say how the colonies are counted

  • @TrouzzzerSnake
    @TrouzzzerSnake 11 лет назад +2

    why call it a plate count when you don't count the plates?

  • @you-dont-know-me
    @you-dont-know-me Год назад +1

    Where can i buy these wicked neon green gloves??

  • @ahmadtalsaadi
    @ahmadtalsaadi 11 лет назад +1

    Sorry: how NOT who

  • @rummanshafi6175
    @rummanshafi6175 4 года назад

    Then u didn't tell how to count the colonies

    • @BioRadEducation
      @BioRadEducation 4 года назад +1

      Hi, Sana! To count colonies, we recommend placing the plate lid-side down (so the agar is up and you're looking at agar underside) on a background that gives you good contrast between the agar and the colonies - for white colonies, a black background works well. Using a felt-tipped pen, dot each colony as you count; by dotting you'll know if you already counted a colony. If the plate has a lot of colonies, use the marker to draw lines on the backside of the plate to mark four equally-sized quadrants, count the colonies in one of the quadrants, and multiply by four for an estimated number of colonies on the plate.