Separation, culture and induction differentiation method for precursor adipocyte in chicken muscle
A technology for inducing differentiation and adipocytes, applied in the field of cytology, can solve the problems of inability to directly separate intramuscular adipose tissue, uneven distribution of poultry intramuscular fat, and inability to effectively separate, achieving unbreakable, good sealing, and induction efficiency high effect
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[0038] In the present embodiment, the method for separating, culturing and inducing differentiation of preadipocytes in chicken muscle comprises the following steps:
[0039] 1) Disinfect 18-day-old (or 14-21 days) old Gushi chickens with bromogeramine, bleed the neck to death, soak in 75% (V:V) alcohol solution for 5 minutes, and work aseptically in the cell room Taiwan for the separation of cells;
[0040] Under aseptic conditions, the chest muscle tissue was collected and put into a preheated PBS petri dish, and the blood vessels, fascia and connective tissue visible to the naked eye were removed (the breast skin, subcutaneous fat and connective tissue were removed with sterile scissors and forceps). The lower pectoralis major muscle was cut out with pre-autoclaved ophthalmic scissors, quickly washed twice in PBS buffer containing double antibodies (100U / mL penicillin and 100U / mL streptomycin), and the tissue block was cut into 1mm 3 Then transfer the shredded tissue to a ...
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