The Gram Stain Procedure

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  • Опубликовано: 26 дек 2024

Комментарии • 53

  • @ginosanchez7
    @ginosanchez7 5 лет назад +77

    can i play this music during my lab practical tmrw??

  • @verah1849
    @verah1849 5 лет назад +8

    This my exam today I'm happy to see that I did it well as required. Thanks for posting.

  • @GonzaloCayoDigital
    @GonzaloCayoDigital 7 лет назад +12

    A lot of thanks, very good video, please DO MORE VIDEOS!!!

  • @ellacalle
    @ellacalle Год назад +2

    What magnification should be used when observing a gram stain? 1000x or 1500x

    • @sci-inspi
      @sci-inspi  Год назад

      Both will work, although 1500X will only look bigger, but not clearer. The limit of light resolution through a light microscope is about 1000X magnification.

  • @Jmpaz2010
    @Jmpaz2010 5 лет назад +9

    Very interesting video. Why aren't the bacteria washed off during any of these steps? Does the "heat fix" keep them in place? Thanks!

    • @sci-inspi
      @sci-inspi  5 лет назад +9

      Correct, the heat fix step sticks them to the slide.

    • @Jmpaz2010
      @Jmpaz2010 5 лет назад +2

      @@sci-inspi Thanks for the quick reply.

    • @aaronrichardtalley
      @aaronrichardtalley 3 года назад +2

      @@sci-inspi Why isnt the crystal violet washed away with the water. it hasnt been mixed with the iodine yet to form the complex that's insoluble in water.

    • @DeShark88
      @DeShark88 Год назад +3

      @@aaronrichardtalley The water cannot penetrate the cell since it is a polar solvent. Therefore it only washes away crystal violet that hasn't penetrated the cell. This is also the reason that alcohol (a nonpolar solvent) is used for the decolorisation step and not water. In fact, even the alcohol can only penetrate those cells that do not have a thick peptidoglycan layer. In that case, the crystal violet is not washed away, and that is how/why this Gram stain procedure works.

  • @abhishekmajumdar4564
    @abhishekmajumdar4564 5 месяцев назад +2

    But we don't use blot paper to dry it, we air dry the slide

    • @sci-inspi
      @sci-inspi  5 месяцев назад +1

      That works too. Some lab techniques differ lab to lab.

  • @yashiraghav3408
    @yashiraghav3408 7 лет назад +2

    Learned and enjoyed watching 😀

  • @vidhiwanjari1704
    @vidhiwanjari1704 5 лет назад

    Very interesting video sir but sir I have one confusion that the smear will be prepare by the process of heat fix?

  • @theshatub962
    @theshatub962 6 лет назад +2

    Good job useful video 👏🏽👏🏽

  • @naveedahmad8407
    @naveedahmad8407 7 лет назад +1

    very helpful video thanx...and next time explain mechanism of the Gram staining...good luck

    • @DeShark88
      @DeShark88 Год назад +1

      See 2:05 for the mechanism.

  • @chinemeogougwu1065
    @chinemeogougwu1065 Год назад

    Wow
    Thank you 😊
    I love it

  • @lil_weasel219
    @lil_weasel219 5 лет назад +2

    Why aren't Gram+ stained by safranin as well?

    • @sci-inspi
      @sci-inspi  5 лет назад +11

      Gram + bacteria have a thick peptidoglycan layer that binds to the crystal violet-iodine complex that doesn't wash off with grams alcohol. so Safranin can't stain it since the CV-I complex is already there. Gram - bacteria don't retain the CV-I complex after washing with grams alcohol. so it is stain with safranin.

  • @brienYT
    @brienYT 2 года назад

    How long do I heat fix the slide for?

    • @DeShark88
      @DeShark88 Год назад

      About as long as was shown in the video. It's usually only two slow passes over the flame.

  • @kamalarani5478
    @kamalarani5478 5 лет назад

    Short n simple... Good

  • @indianstars2405
    @indianstars2405 6 лет назад +2

    Can i use cover clip

    • @sci-inspi
      @sci-inspi  6 лет назад

      Yes, a coverslip can be used.

  • @devarshjoshi5839
    @devarshjoshi5839 15 дней назад

    bruhh the electric guitar is legit😂😂

  • @kratichouhan4032
    @kratichouhan4032 21 день назад

    Meri slides nahi dikh thi

  • @icediverfull
    @icediverfull 5 лет назад

    Thanks you, very nice Video

  • @Jrodrig1138
    @Jrodrig1138 6 лет назад +1

    Thank you!!!

  • @nicolekrantz2172
    @nicolekrantz2172 7 лет назад +1

    Very cool!

  • @genanhamideh3097
    @genanhamideh3097 5 лет назад +1

    don't you have to put acetone for less than a second? or does it matter?

    • @sci-inspi
      @sci-inspi  5 лет назад +2

      This protocol says 10-20 seconds. I have gram stains that come out fine following this protocol.

    • @kamalarani5478
      @kamalarani5478 5 лет назад

      No need

    • @DeShark88
      @DeShark88 Год назад

      There are different decolourisers used in Gram staining. Acetone can bleach the dye somewhat, but alcohol will not. So, it depends what decolouriser is used.

  • @sappuprajapati2345
    @sappuprajapati2345 Год назад

    Very nice

  • @arunpratapsingh3145
    @arunpratapsingh3145 3 года назад

    Awesome ☺️

  • @dhananjayasingh2838
    @dhananjayasingh2838 5 лет назад

    Gram + ve bacteria is coccus and Gram -ve bacteria is rod shaped👍

    • @timetravelerboutique8009
      @timetravelerboutique8009 5 лет назад +4

      Gram positive stains purple, and gram negative stains pink. Both include cocci and rods. Anthrax, for example, is a Gram positive rod.

  • @rawyhjamal5215
    @rawyhjamal5215 5 лет назад

    A lot of thanks

  • @SaadSaad-mb4py
    @SaadSaad-mb4py 4 года назад

    Fantastic

  • @Nova-ke7pk
    @Nova-ke7pk 3 года назад

    Thank u

  • @laurenodom7779
    @laurenodom7779 Год назад +1

    forgot the wax ring and water droplet

  • @wondimw320
    @wondimw320 2 года назад

    good

  • @nursepotassium
    @nursepotassium 3 года назад

    Staphylococcus 💜

  • @jai.m1934
    @jai.m1934 3 года назад

    Better than danish grams

  • @xaazoozaa856
    @xaazoozaa856 5 лет назад

    my exam is tommorw

  • @NarenManoj7
    @NarenManoj7 5 лет назад

    👍

  • @SAX-cl6lk
    @SAX-cl6lk 5 лет назад

    nice but we didnt need so much jimi hendrix in thebackround

    • @qmac9966
      @qmac9966 5 лет назад +6

      I beg to differ