Method for separating and culturing poultry bone mesenchymal stem cells by using bone marrow tissue block
A bone marrow mesenchymal and bone marrow tissue technology, applied in the field of stem cell isolation and culture, can solve the problems of cell cloning ability, low subculture and expansion ability, poor cell differentiation potential in acquisition rate, and difficulty in BMSC separation. Good differentiation potential, reduced cell damage, and good proliferation potential
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Embodiment 1
[0027] Example 1 Isolation and culture of chicken bone marrow mesenchymal stem cells
[0028] (1) Isolation and primary culture of chicken bone marrow mesenchymal stem cells
[0029] Take the femur and humerus of 5-day-old white legion chicken, remove the epiphysis at both ends, cut the bone with bone scissors, take out the bone marrow and put it in a 5ml centrifuge tube, and cut it to 1-2mm with surgical scissors 3 , add 800 μl of fetal bovine serum, blow slowly with a pipette to suspend the bone marrow fragments, transfer to a 100mm petri dish, arrange with a pipette so that the bone marrow fragments are evenly distributed in the petri dish, put the petri dish into carbon dioxide culture Box, 37°C, 90% humidity, 5% CO 2 After placing it at an angle of 60 degrees for 60 minutes, take out the culture dish, suck up the serum in the culture dish, slowly add complete culture solution (low-sugar DMEM culture solution containing 10% fetal bovine serum), and cultivate for 3 days to...
Embodiment 2
[0038] Example 2 Isolation and culture of duck bone marrow mesenchymal stem cells
[0039] (1) Isolation and primary culture of duck bone marrow mesenchymal stem cells
[0040] Take the femur and humerus of a 3-day-old Peking duck, remove the epiphysis at both ends, cut the bone with bone scissors, take out the bone marrow and put it in a 5ml centrifuge tube, and cut it to 1-2mm with surgical scissors 3 , add 500 μl of fetal bovine serum, blow slowly with a pipette to suspend the bone marrow fragments, transfer to a 100mm petri dish, arrange with a pipette so that the bone marrow fragments are evenly distributed in the petri dish, put the petri dish into carbon dioxide culture Box, 37°C, 90% humidity, 5% CO 2 After placing it at an angle of 45 degrees for 40 minutes, the culture dish was taken out, the serum in the culture dish was aspirated, and complete culture solution (low-sugar DMEM culture solution, 10% fetal bovine serum) was slowly added, and cultured for 3 days to ob...
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