A method for immunofluorescence staining of suspension cells
A technology of immunofluorescence staining and staining method, which is applied in the preparation of test samples, etc., to achieve good staining results
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[0032] 1. Experimental materials
[0033] Cells: Mouse iPS cells (induced pluripotent stem cells, induced pluripotent stem cells), cultured in a bacterial culture dish for 5 days to form embryoid bodies (EBs), added 2um of retinoic acid (RA) and cultured for 2 days to induce differentiation EB cells.
[0034] Reagents: 4% paraformaldehyde, phosphate buffer (Hyclone), 1% BSA (Sigma), TritonX-100, primary antibody VASA rabbit anti-mouse (Abcam), fluorescent secondary antibody A11072 goat anti-rabbit (Invitrogen), DAPI, Mounting medium (DAKO).
[0035] Equipment: low-speed centrifuge (Thermo), low-speed shaker, ordinary refrigerator (Midea), laser confocal microscope (Leica).
[0036] 2. Experimental method
[0037] 1. Collect the RA-induced EB cell mass in a 2ml centrifuge tube;
[0038] 2. Add 2ml of PBS, gently invert several times, centrifuge at 800g for 5min, and discard the supernatant;
[0039] 3. Repeat step 2;
[0040] 4. Add 2ml of distilled water, gently invert s...
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