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Kit for inducing differentiation from bone mesenchymal stem cells to fat cells, application of kit and method for inducing cell differentiation

A bone marrow mesenchymal and adipocyte technology, applied in the field of cell differentiation induction kit and its application and induction cell differentiation, can solve the problems of increasing uncertainty and risk

Inactive Publication Date: 2011-05-04
GENERAL HOSPITAL OF PLA
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  • Abstract
  • Description
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Problems solved by technology

However, studies have found that bone marrow mesenchymal stem cells can be induced to differentiate into adipocytes for as long as 3-4 weeks, which adds uncertainty and risk to the experiment

Method used

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  • Kit for inducing differentiation from bone mesenchymal stem cells to fat cells, application of kit and method for inducing cell differentiation
  • Kit for inducing differentiation from bone mesenchymal stem cells to fat cells, application of kit and method for inducing cell differentiation
  • Kit for inducing differentiation from bone mesenchymal stem cells to fat cells, application of kit and method for inducing cell differentiation

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Embodiment Construction

[0037] The substantive content of the present invention will be further described below in conjunction with the implementation of the present invention, but the present invention is not limited thereto. The test materials used in the present invention, unless otherwise specified, are commercially available products.

[0038] 1. Preparation of a kit for inducing the differentiation of rat bone marrow mesenchymal stem cells into adipocytes

[0039] (1) Solution preparation

[0040] The kit for preparing rat bone marrow mesenchymal stem cells of the present invention includes the following preparations:

[0041] 1. Adipocyte induction culture medium: including cell culture medium A, cell culture medium B, cell culture medium C, cell culture medium D, and cell culture medium E. Wherein, the cell culture solution A is α-MEM liquid medium; the cell culture solution B is fetal bovine serum; the cell culture solution C is 1 mM dexamethasone solution; the cell culture solution D is 0...

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Abstract

The invention provides a kit and method for inducing differentiation from rat bone mesenchymal stem cells to fat cells. The kit comprises a fat cell inducing culture solution and a fat cell identification solution, wherein the inducing culture solution comprises a cell culture solution A, a cell culture solution B, a cell culture solution C, a cell culture solution D and a cell culture solution E; the fat cell identification solution comprises a cell immobilizing solution, a coloring agent, a detergent A and a detergent B; the cell culture solution A is an alpha-minimum essential medium (MEM) liquid culture medium; the cell culture solution B is fetal bovine serum; the cell culture solution C is a dexamethasone solution; the cell culture solution D is a 1-methyl-3-isobutylxanthine solution; the cell culture solution E is an insulin solution; the cell immobilizing solution is a paraformaldehyde solution; the coloring agent is an oil red O solution; the detergent A is a 60% isopropanol solution; and the detergent B is double distilled water.

Description

technical field [0001] The present invention relates to a kit for inducing cell differentiation and its application and a method for inducing cell differentiation, in particular to a kit for inducing differentiation of bone marrow mesenchymal stem cells to fat cells and its application and method for inducing bone marrow mesenchymal stem cells A method for the differentiation of stem cells into fat cells. Background technique [0002] Bone marrow mesenchymal stem cells are a type of adult stem cells with multi-directional differentiation potential, which can be differentiated into adipocytes, chondrocytes, adipocytes, nerve cells, liver cells and other tissue cells, which can be applied clinically in tissue engineering and gene therapy , cytokine replacement therapy and other fields. [0003] Bone marrow mesenchymal stem cells are a group of cells with unique phenotypes. Due to the lack of specific surface markers, how to determine whether the obtained cell clones are bone ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N5/0775C12N5/077
Inventor 杨仕明秦贺赵立东翟所强郭维维孙建和杨伟炎
Owner GENERAL HOSPITAL OF PLA
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