Storage method of adipose-derived stem cells
An adipose stem cell and storage method technology, applied in the preservation, application, animal husbandry and other directions of human or animal body, can solve the problems of low cell viability, cell oxidative damage, etc., to expand blood volume, improve viability, and eliminate blood vessels. Efficacy of endoerythrocyte aggregation and thrombosis
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0022] A method for storing fat stem cells, the specific steps are as follows:
[0023] (1) separating and culturing adipose stem cells from adipose tissue;
[0024] (2) Add the fat stem cells described in step (1) into the cell cryopreservation tube equipped with the fat stem cell storage solution, and seal the mouth of the tube; the concentration of the fat stem cells is 1×10 6 a / mL;
[0025] Wherein, every 100mL of said adipose stem cell storage solution consists of the following components and contents:
[0026] 2g carboxylated poly-L-lysine, 5g trehalose, 1.5mL DMSO, 8mL glycerol, 25mL serum-free medium, 1mL low molecular weight dextran, 3g glucose, penicillin 100U / mL, streptomycin 100μg / mL, The amount is PBS buffer solution;
[0027] (3) Freezing the sealed cell cryopreservation tube described in step (2).
Embodiment 2
[0029] A method for storing fat stem cells, the specific steps are as follows:
[0030] (1) separating and culturing adipose stem cells from adipose tissue;
[0031] (2) Add the adipose stem cells described in step (1) into the cell cryopreservation tube equipped with the adipose stem cell storage solution, and seal the mouth of the tube; the concentration of the adipose stem cells is 0.5×10 6 a / mL;
[0032] Wherein, every 100mL of said adipose stem cell storage solution consists of the following components and contents:
[0033] 0.6g carboxylated poly-L-lysine, 1g trehalose, 1mL DMSO, 6mL glycerol, 20mL serum-free medium, 0.2mL low molecular weight dextran, 2g glucose, penicillin 80U / mL, streptomycin 75μg / mL, The balance is PBS buffer solution;
[0034] (3) Freezing the sealed cell cryopreservation tube described in step (2).
Embodiment 3
[0036] A method for storing fat stem cells, the specific steps are as follows:
[0037] (1) separating and culturing adipose stem cells from adipose tissue;
[0038] (2) Add the adipose stem cells described in step (1) into the cell cryopreservation tube equipped with the adipose stem cell storage solution, and seal the mouth of the tube; the concentration of the adipose stem cells is 2×10 6 a / mL;
[0039] Wherein, every 100mL of said adipose stem cell storage solution consists of the following components and contents:
[0040] 4g carboxylated poly-L-lysine, 10g trehalose, 3mL DMSO, 10mL glycerol, 30mL serum-free medium, 2mL low molecular weight dextran, 5g glucose, penicillin 90U / mL, streptomycin 85μg / mL, balance For HEPES buffer;
[0041] (3) Freezing the sealed cell cryopreservation tube described in step (2).
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.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap