Mass spectrum flow cytometer detection kit capable of accurately typing tumor immune cell subsets
An immune cell and flow cytometric detection technology, applied in the field of cell biology, can solve the problem of lack of comprehensive, dynamic and accurate description of immune cell subpopulation system, achieve accurate typing and save samples
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[0021] Embodiment 1 tests the staining effect of 42 kinds of antibodies
[0022] 1. Prepare fresh normal human peripheral blood and extract immune cells.
[0023] 2. Divide the immune cells into two groups, the control group and the experimental group, with about 3x10^6 cells in each group, resuspend them in PBS, adjust the volume to 1 mL, add 194Pt, and stain at room temperature for 2 minutes to distinguish the dead and alive cells.
[0024] 3. Add 2mL bovine serum albumin solution, centrifuge at 500g / 5min, remove the supernatant, add 50uL blocking solution (0.5uL human immunoglobulin solution, 0.5uL mouse immunoglobulin solution, 0.5uL rat immunoglobulin solution , 0.5uL hamster immunoglobulin solution, 48uL bovine serum albumin solution), and block on ice for 20min.
[0025] 4. Add 50uL bovine serum albumin solution to the control group as a blank control, add 50uL extracellular antibody mixture (0.5ul each of the 35 extracellular antibodies in Table 1, 32.5ul bovine serum...
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