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- Anna is training to be a cell culture technician. She uses some sterile distilled water to wasg a batch of cell culture plates. When she looks at the cell culture plates under the microscope to check the cells after this, she notices the cell have burst. She realizes she should have used 0.9% saline instead. Explain what has happened, and why she should have used the saline.Why is a viable count more sensitive than a microscopic count?What major assumption is made in relating plate count resultsto cell number?You counted 4, 6, 12, 3 cells in each of the 4.outed squares of a hemacytomeyer. What are the cells per milliliter in that culture? If you resuspended your cell pellet 2.5 mL, what is the total cell count? How many uL do you need to add to a new culture if you want 4250 cells?
- How does the microscopy in Figure 2 show that the capsule and an S-layer can exist in the same cell at the same time? I need help finding the answer in the article and explain in short answer link to article: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC106848/Beginning with 2.0 ×104 cells/L, outline the Evans Blue method for counting viable and dead cells.Complete the following: After comparing the wet mount and the stained cheek cells, state the advantage that was gained by staining cells...............................
- Write down a comparison of the sizes of the untreated cell and the colchicine-treated cell.Which stain is used to diagnose hairy cell leukemia? Question 14 options: A) Sudan Black B B) MPO C) LAP D) TRAPlabel cell structures. the photo is of stained mammalian cellsthat are under under a compound light microscope at 400x total magnification. the cells were treated with cell fixing agent, methylene blue stain, and eosin stain.