Medium for human umbilical blood mesenchymal stem cells and culture method thereof
A technology of mesenchymal stem cells and culture methods, which is applied in the medium of umbilical cord blood mesenchymal stem cells and its culture field, can solve the problems of low culture efficiency and limited application, and achieve the purpose of improving the ability of proliferation, maintaining phenotype and characteristics, and promoting The effect of cell proliferation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0047] (1) Experimental grouping
[0048] Table 1 Experimental Grouping Situation
[0049] group
Medium composition
control group
DMEM / F12+10%FBS
Experimental group 1
DMEM / F12+10%PRP
Experimental group 2
DMEM / F12+1mg / mL astragalus polysaccharide
Experimental group 3
DMEM / F12+10%PRP+1mg / mL astragalus polysaccharide
[0050] (2) Adult autologous serum preparation
[0051] The peripheral blood of normal volunteers was drawn into a sterile glass bottle and placed in an incubator for 2 hours. After the blood clot was precipitated, the serum was aspirated and transferred into a centrifuge tube, centrifuged at 1500 rpm for 20 minutes at low temperature, the precipitate was discarded, and PRP was obtained and stored in aliquots. Inactivate in a 60°C water bath for 20 minutes before use, and store in a 4°C refrigerator for later use. Prepare the medium as in the experimental grouping.
[0052] (3) Primary isolation of u...
Embodiment 2
[0075] (1) Experimental grouping
[0076] Table 4 Experimental Grouping Situation
[0077] group
Medium composition
control group
DMEM / F12+10%FBS
Experimental group 1
DMEM / F12+8%PRP
Experimental group 2
DMEM / F12+0.5mg / mL astragalus polysaccharide
Experimental group 3
DMEM / F12+8%PRP+0.5mg / mL astragalus polysaccharide
[0078] (2) Adult autologous serum preparation
[0079] The peripheral blood of normal volunteers was drawn into a sterile glass bottle and placed in an incubator for 2 hours. After the blood clot was precipitated, the serum was aspirated and transferred into a centrifuge tube, centrifuged at 1500 rpm for 20 minutes at low temperature, the precipitate was discarded, and PRP was obtained and stored in aliquots. Inactivate in a 60°C water bath for 20 minutes before use, and store in a 4°C refrigerator for later use. Prepare the medium as in the experimental grouping.
[0080] (3) Primary isolation of...
Embodiment 3
[0103] (1) Experimental grouping
[0104] Table 7 Experimental Grouping Situation
[0105] group
Medium composition
control group
DMEM / F12+10%FBS
Experimental group 1
DMEM / F12+5%PRP
Experimental group 2
DMEM / F12+0.1mg / mL astragalus polysaccharide
Experimental group 3
DMEM / F12+5%PRP+0.1mg / mL astragalus polysaccharide
[0106] (2) Adult autologous serum preparation
[0107] The peripheral blood of normal volunteers was drawn into a sterile glass bottle and placed in an incubator for 2 hours. After the blood clot was precipitated, the serum was aspirated and transferred into a centrifuge tube, centrifuged at 1500 rpm for 20 minutes at low temperature, the precipitate was discarded, and PRP was obtained and stored in aliquots. Inactivate in a 60°C water bath for 20 minutes before use, and store in a 4°C refrigerator for later use. Prepare the medium as in the experimental grouping.
[0108] (3) Primary isolation of...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 