Preparation method of culture medium simulating diabetic foot inflammation micro environment
A technology of diabetic foot and preparation process, which is applied in the direction of culture process, tissue culture, cell culture active agent, etc., can solve the problem of lack of stem cell culture medium, and achieve the effect of good compatibility, appropriate pH and high specificity
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[0017] Use a pipette or a pipette gun to accurately measure 10ml of DMEM / F12 medium, 2ml of fetal bovine serum, 300μl of non-essential amino acids, 300μl of L-glutamine, 200ng of vascular cell adhesion molecule-1, 250ng of tumor necrosis factor α, 200ng of interleukin-6, placed in the same 20ml test tube; vortex the test tube on an automatic vortexer for 10 minutes to fully mix the components; put the fully mixed components into a petri dish and freeze in a 4° refrigerator; According to the number of cells and survival rate, use this medium to adjust the cell inoculation density to 1.0×104 live cells / cm2, add the cell suspension into the culture bottle, shake gently to make the cells evenly distributed; mark it on the culture bottle , transferred to a CO2 incubator with 5% CO2, 37°C, and a saturated humidity of 95%. Observe the state of the cells, and change the medium every other day; when the confluence of the cells reaches 80-90%, they can be subcultured.
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