High-purity duck intramuscular precursor fat cell separation method
A technology of adipocytes and separation methods, which is applied to the separation of preadipocytes in meat duck muscle, the isolation of high-purity preadipocytes in duck muscle, culture and induced differentiation, which can solve the problem of reducing the economic value of carcass and affecting feed conversion Efficiency and other issues
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[0030] In this embodiment, the process of isolation, culture and induction of preadipocytes in meat duck muscle is as follows:
[0031] 1. Soak 8-day-old ducklings in bromogeramine solution. After 3 minutes, the carotid artery was bled to death, then soaked in 75% ethanol for 5 minutes, and the breast muscle tissue was collected and placed in a preheated 2% double-antibody solution. In PBS buffer, work on separating cells between cells.
[0032] 2. Soak the collected pectoral muscle tissue in 75% alcohol for 1 min, transfer to 2% double-antibody PBS buffer, wash 3 times, and remove the visible fascia with high-pressure scissors and tweezers. Transfer the tissue block to a vial and cut it into 1mm 2 Then transfer the shredded tissue pieces to a 50ml centrifuge tube, add 10 times the volume of 0.1% type Ⅰ and type Ⅱ collagenase mixture (the volume ratio of type Ⅰ and type Ⅱ collagenase is 1:1), and put Seal it with a parafilm, shake it at 37°C, and digest it for 1 hour. At thi...
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