Method for differentiating fat cells by oriented inducing chick embryo primordial germcell
A technology for differentiation of primordial germ cells and adipocytes, applied in biochemical equipment and methods, animal cells, vertebrate cells, etc., can solve the problems of few research reports on chicken EPGCs, achieve strong repeatability, scientific and reasonable preparation, The effect of easy operation
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[0018] 1. Preparation of inducer
[0019] ①Inducer I: 90%DMEM+10%FBS+5.5×10 -5 β-mercaptoethanol+1×10 -6 mol / L dexamethasone+10mg / L insulin+5×10 -4 mol / L 3-isobutyl-1-methylxanthine.
[0020] ②Inducer II: 90%DMEM+10%FBS+5.5×10 -5 β-mercaptoethanol + 10mg / L insulin.
[0021] 2. Isolation, culture and passage of chicken embryo primordial germ cells
[0022] The EPGCs aggregated in the gonads were extracted at the 19th and 28th stages of chicken embryo development by a separate enzyme dissociation method, and the extracted cells were inoculated on the prepared feeder layer, and added with 10% fetal bovine serum, 2% chicken serum, 2mmol / L L-glutamine, 1mmol / L sodium pyruvate, 5.5×10 -5 mol / L β-mercaptoethanol, 10μl / ml non-essential amino acids, 10IU / ml murine leukemia inhibitory factor (mLIF), 5ng / ml human stem cell growth factor (hSCF), 10ng / ml basic fibroblast growth factor (bFGF), 0.04ng / ml human interleukin-11 (hIL-11), 10ng / ml insulin-like growth factor (hIGF) in high-...
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