Problems that should be paid attention to when using flow cytometry to count cells
Problems that should be paid attention to when using flow cytometry to count cells
After making tissue homogenate or cell suspension and staining with fluorescent dye, you can use flow cytometry to count the number of cells with different DNA content or multiples. For example, in testicular tissue, sperm cells are haploid cells, spermatogonium cells, Sertoli cells, Leydig cells, and other non-spermatogenic cells are diploid cells, primary spermatocytes, and spermatogonium cells and non-squamous cells in the dividing stage Spermatogenic cells are tetraploid cells. Therefore, using flow cytometry to determine the changes in DNA ploidy of spermatogenic cells at all levels of testicular tissue can indirectly determine the trend of the relative proportion of different spermatogenic cell numbers. However, you must be cautious when using these results to draw conclusions. For example, a decrease in the percentage of haploid cells may indicate a decrease in the number of sperm cells, but the following three conditions may also cause a decrease in the percentage:
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