Culture medium for amniotic fluid and chorionic villus
A culture medium and basal medium technology, applied in the field of cell biology, can solve the problems of few mitotic phases, ineffective use of amniotic fluid cell inspection, low success rate, etc., to increase the clone formation rate, facilitate product scale, and clone growth The effect of speed increase
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preparation example 1
[0042] Prepare HEPES / NaHCO with a concentration of 20mmol / L 3 buffer system
[0043] Take 4.76g HEPES and dissolve in 900ml water for injection, and use 1.5~3g NaHCO 3 Adjust the pH of the aqueous solution to 7, then dilute to 1000ml with water for injection, and store at 4°C.
preparation example 2
[0045] Preparation of Penicillin and Streptomycin Double Antibody Stock Solution
[0046] a) Take 1 bottle of penicillin, 1 million units, and add water to dilute it to 200,000 units / ml.
[0047] b) Take a bottle of 800,000 units of streptomycin and dilute it with water to 200,000 units / ml.
[0048] c) Mix a and b in equal proportions and store at 4°C.
Embodiment 1
[0049] Embodiment 1 (A-1 medium):
[0050] Take 1L of DMEM / F12 cell culture medium, dissolve it with 950ml of water for injection, add 10mmol HEPES / NaHCO3 buffer, add 50,000 units of fibroblast growth factor, 10,000 units of epidermal growth factor, 40,000 units One unit of lymphocyte growth factor, 0.3 g of ascorbyl glucoside, 50,000 units of penicillin, and then dilute to 1000 ml with water for injection.
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