Multifunctional intimal stem cell hematopoietic molecular materials and methods
A technology of pluripotent stem cells and molecular materials, applied in the field of biopharmaceuticals, can solve the problems of inability to achieve differentiation induction, high technical requirements, and high differentiation costs, and achieve the effects of low cost of biological research and development, high differentiation efficiency, and high safety
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Embodiment 1
[0042] Example 1: According to traditional culture methods, multi-functional endometrial stem cell hematopoietic molecular materials and methods, mammalian body fluids were extracted by centrifugation and ultrafiltration to extract somatic cells and injected into bFGF cell proliferation and differentiation regulator with a final concentration of 39ng / ml. Encapsulated in medium No. 1 for culture, senescent or damaged pluripotent hematopoietic stem cells in mammals were used to access medium No. 2 for culture, and the final concentration of 50ng / ml of L-Valley was injected into the medium. Aminoamide reagent, take the osteoblasts or sinusoidal endothelial cells on the surface of the endosteum and trabecular bone of mammals and inject them into culture medium No. 3, and inject insulin with a final concentration of 60ng / ml. Oct4, Sox2, Nanog and The retrovirus of the four transcription factors of LIN28 was transferred into medium No. 4, and the final concentration of 30ng / ml vitami...
Embodiment 2
[0043] Embodiment 2: On the basis of Embodiment 1, the sodium pyruvate solution reagent with a final concentration of 40ng / ml is added dropwise on the basis of the original materials of each culture medium, and then the multifunctional endometrial stem cell hematopoietic molecular material and method are obtained. , take mammalian body fluids, extract somatic cells by centrifugation and ultrafiltration, inject bFGF cell proliferation and differentiation regulator with a final concentration of 39ng / ml, and then seal them into medium No. 1 for culture. Pluripotent hematopoietic stem cells were cultured in culture medium No. 2, and L-glutamine reagent with a final concentration of 50ng / ml and sodium pyruvate solution reagent with a final concentration of 40ng / ml were injected into the medium. The osteoblasts or sinusoidal endothelial cells on the surface of the endosteal and trabecular bone were injected into the medium No. 3, and the final concentration of 60ng / ml of insulin and ...
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