Process for separation and culture of marrow mesenchyme stem cell
A technology of bone marrow mesenchyme and culture method, applied in the biological field, can solve the problems of low cell viability and large cell damage, and achieve the effect of good proliferation, fast growth speed and good growth condition
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Benefits of technology
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0037] (1) Primary culture:
[0038] Femur tissue from four-month-old fetuses who died after induction of labor by the water bag method was collected, cells in the bone marrow cavity were washed with D-Hank's solution, and centrifuged at 1200 rpm for 8 minutes after collection; the supernatant was discarded after centrifugation, and the cell pellet was blown with mixed culture medium I to make Form a cell suspension and perform cell counting; take the mixed culture solution I containing cells, and press the cell culture density of 1×10 6 Inoculate each cell / bottle into a 100ml cell culture bottle, make up to 8-10ml of the total culture medium with mixed culture solution I, culture for two days according to routine, discard half of the original medium, and then add 5ml of fresh mixed culture Solution I was placed in a carbon dioxide incubator to continue culturing.
[0039] (2) Subculture:
[0040] After the cells entered the logarithmic growth phase, remove the cell culture ...
Embodiment 2
[0048] (1) Primary culture:
[0049] Femur tissue from four-month-old fetuses who died after induction of labor by the water bag method was collected, cells in the bone marrow cavity were washed with D-Hank's solution, and centrifuged at 1200 rpm for 7 minutes after collection; the supernatant was discarded after centrifugation, and the cell pellet was blown with mixed culture medium I to make Form a cell suspension and perform cell counting; take the mixed culture solution I containing cells, and press the cell culture density of 1.5×10 6 1 cell / bottle, inoculated in a 100ml cell culture bottle, supplemented with mixed culture solution I until the total amount of culture solution was 8-10ml, cultured for two days as usual, discarded half of the original medium, and then added 4ml of fresh mixed Culture solution I was placed in a carbon dioxide incubator to continue culturing.
[0050] (2) Subculture:
[0051] After the cells entered the logarithmic growth phase, remove the ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com