Preparation method and application of induced pluripotent stem cell secretin
A technology of pluripotent stem cells and secretin, applied in the biological field, can solve problems such as difficult cultivation, achieve good results, increase yield, and be suitable for large-scale production
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Embodiment 1
[0022] Example 1 A preparation method of induced pluripotent stem cell secretin
[0023] The preparation method comprises the following steps:
[0024] S1 resuspended induced pluripotent stem cells to obtain induced pluripotent stem cell suspension;
[0025] S2 Distribute the induced pluripotent stem cell suspension obtained in step S1 on a three-dimensional carrier, and place the induced pluripotent stem cell culture medium IMDM / F12+2mg / mL human albumin+40μg / mL vitamin C+3mg / mL in a bioreactor In ginsenoside monomer Rb1, at 37°C, 5% CO 2 Induced pluripotent stem cells were obtained by culturing under conditions for 24 hours;
[0026] S3 In step S2, at the vigorous stage of induced pluripotent stem cell division, rinse the induced pluripotent stem cells and the three-dimensional carrier twice with 0.01M phosphate buffer (pH=7.3), and then add the basic culture medium IMDM / F12 and Phosphate buffer (volume ratio: 1:2) was continued to cultivate for 6h, and the supernatant in ...
Embodiment 2
[0028] Example 2 A preparation method of induced pluripotent stem cell secretin
[0029] The preparation method comprises the following steps:
[0030] S1 resuspended induced pluripotent stem cells to obtain induced pluripotent stem cell suspension;
[0031] S2 Distribute the induced pluripotent stem cell suspension obtained in step S1 on a three-dimensional carrier, and place the induced pluripotent stem cell culture medium IMDM / F12+3mg / mL human albumin+50μg / mL vitamin C+5mg / mL in a bioreactor In ginsenoside monomer Rb1, at 37°C, 5% CO 2 Induced pluripotent stem cells were obtained by culturing under conditions for 48 hours;
[0032] S3 In step S2, at the vigorous stage of induced pluripotent stem cell division, wash the induced pluripotent stem cells and the three-dimensional carrier with 0.01M phosphate buffer (pH=7.3) for 3 times, and then add the basal culture medium IMDM / F12 and Phosphate buffer (volume ratio: 1:4) was further cultivated for 15 hours, and the supernat...
Embodiment 3
[0034] Example 3 A preparation method of induced pluripotent stem cell secretin
[0035] The preparation method comprises the following steps:
[0036] S1 resuspended induced pluripotent stem cells to obtain induced pluripotent stem cell suspension;
[0037] S2 Distribute the induced pluripotent stem cell suspension obtained in step S1 on a three-dimensional carrier, and place the induced pluripotent stem cell culture medium IMDM / F12+4mg / mL human albumin+60 μg / mL vitamin C+7mg / mL in a bioreactor In ginsenoside monomer Rb1, at 37°C, 5% CO 2 Induced pluripotent stem cells were obtained by culturing under conditions for 72 hours;
[0038] S3 In step S2, at the vigorous stage of induced pluripotent stem cell division, wash the induced pluripotent stem cells and the three-dimensional carrier with 0.01M phosphate buffer (pH=7.3) for 3 times, and then add the basal culture medium IMDM / F12 and Phosphate buffer (volume ratio: 1:6) was continued to cultivate for 24 hours, and the sup...
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