Induction medium for inducing human adipose tissue-derived stromal cells as nerve cells and method
A technology for inducing mesenchymal stem cells, which is applied in the field of inducing differentiation medium, can solve the problems of high cell death rate, long induction time, and low induction efficiency, and achieve high induction success rate, short induction time, and high induction efficiency. Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Example 1 An induction medium for inducing human adipose-derived mesenchymal stem cells into neurons in this example is composed of liquid A, liquid B, and liquid C, and is prepared by the following method:
[0025] Solution A: Dissolve 10ug bFGF (basic fibroblast growth factor, peprotech, 96-100-18B-50) in 500ml of human mesenchymal stem cell serum-free medium (LONZA, product number 00190632), filter and sterilize to obtain A solution, in which bFGF concentration is 20ng / ml;
[0026]Solution B: Add 10ml of Xiangdan injection (active ingredient Danshensu, Jiangsu Changshu Leiyunshang Pharmaceutical Co., Ltd.) into 490ml of human mesenchymal stem cell serum-free medium to obtain solution B, wherein the final volume concentration of Xiangdan injection is 2%;
[0027] Solution C: 5ug bFGF, 5ug EGF (epidermal growth factor, peprotech, 96-AF-100-15-500), 50ug BDNF (brain-derived neurotrophic factor, peprotech, catalog number 450-02), 100ug GM1 (ganglioside Lipid, Sigma, G7...
Embodiment 2
[0028] Example 2 The method for inducing differentiation of human adipose-derived mesenchymal stem cells into neurons by using the induction medium of the present invention, the steps are as follows:
[0029] 1. Preparation of human adipose-derived mesenchymal stem cells:
[0030] 1. To receive adipose tissue, wipe the outer wall of the container containing adipose tissue with 75% alcohol;
[0031] 2. Dispense adipose tissue, each T175 culture bottle is divided into 50ml adipose tissue. With a 10ml pipette, remove the tip, first absorb the lower layer of red liquid in the fat collection bottle and discard it, and mix the remaining upper layer of fat before subpackaging.
[0032] 3. Wash fat tissue and remove blood cells. Add 100ml of sodium chloride injection into the T175 culture bottle, tighten the cap, shake vigorously for 3 minutes to fully wash the adipose tissue, then stand still for 3 to 5 minutes to separate the different phases, and suck off the lower aqueous phase;...
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