Microbiology: How to perform a Primary Set up from a Positive Blood Culture

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  • Опубликовано: 25 дек 2024

Комментарии •

  • @misbahalam9861
    @misbahalam9861 3 года назад +2

    Thanks for the demonstration

  • @nashidul09471
    @nashidul09471 Год назад +3

    Why are you using same inoculating loop on every agar media for streaking 😒

  • @ghidanasr6706
    @ghidanasr6706 Год назад

    shouldnt we do the gram stain before the isolation on the 3 agars? ( blood, MC, chocolate)

  • @TPruet87
    @TPruet87 4 года назад

    where are you located? and why are you using Trek?

  • @karthimurugan3048
    @karthimurugan3048 2 года назад +1

    Your used Media name mention ?

    • @MedicalLabLadyGill
      @MedicalLabLadyGill  2 года назад +1

      Sheep Blood Agar Plate, Chocolate Agar Plate, and McConkey Agar Plate

    • @karthimurugan3048
      @karthimurugan3048 2 года назад

      @@MedicalLabLadyGill okay thanks for information ✌️🙌 I'm also lab technician ✌️✌️✌️

  • @abrahamelizabeth415
    @abrahamelizabeth415 2 года назад

    What did you do to the specimen after it dried up on the slide

    • @wilfredofosu6908
      @wilfredofosu6908 Год назад

      After the blood sample dries up on the glass microscope slide, you are now ready to begin the Gram Staining procedure which identifies the bactera as Gram Positive or Gram Negative. However, Gram Variables can also be observed. The reagents used for the Gram Stain include, Crystal Violet Dye, Iodine (a mordant), Acetone-alcohol (the decolourizer), and Safranin.

  • @alhiderry2149
    @alhiderry2149 11 месяцев назад

    why you use old plates use after that😮

  • @morganschulz3067
    @morganschulz3067 3 года назад

    So why aren’t we using CNA for blood cultures