生物来源
human bone marrow
包装
pkg of 500,000 cells
制造商/商品名称
Cell Applications, Inc
生长模式
Adherent
核型
2n = 46
形态学
stromal
技术
cell culture | mammalian: suitable
相关疾病
tuberculosis
运输
dry ice
储存温度
−196°C
一般描述
Lot specific orders are not able to be placed through the web. Contact your local sales rep for more details.
Bone marrow is the major blood creating organ, but in addition to supporting hematopoietic growth and differentiation, marrow stromal cells can be induced to produce cells of other connective tissues, such as bone, cartilage, and fat, as well as cells from neuroectodermal (neurons) and endodermal (hepatocytes) lineages. The potential of HMSCs to maintain multipotency and proliferate extensively in vitro provides new avenues for cell-based therapy in the restoration of damaged or diseased tissue.
HMSC have been utilized to investigate the effects of TGF-β1 on differentiation toward different lineages, and show that it inhibits adipogenic differentiation and induces either chondrogenic, osteogenic or smooth muscle cell differentiation, depending the specific culture conditions (Zhao, 2011); to develop methods to assess differentiation potential of stem cells without the differentiation induction (Hirota, 2011); to compare HLA expression profiles of bone marrow-derived and adipose-derived stem cells (Purandare, 2013); and to design heart valve-shaped tri-layered collagen-based constructs for stem cell seeding and differentiation to use in heart valve tissue engineering (Tedder, 2010, 2011).
Bone marrow is the major blood creating organ, but in addition to supporting hematopoietic growth and differentiation, marrow stromal cells can be induced to produce cells of other connective tissues, such as bone, cartilage, and fat, as well as cells from neuroectodermal (neurons) and endodermal (hepatocytes) lineages. The potential of HMSCs to maintain multipotency and proliferate extensively in vitro provides new avenues for cell-based therapy in the restoration of damaged or diseased tissue.
HMSC have been utilized to investigate the effects of TGF-β1 on differentiation toward different lineages, and show that it inhibits adipogenic differentiation and induces either chondrogenic, osteogenic or smooth muscle cell differentiation, depending the specific culture conditions (Zhao, 2011); to develop methods to assess differentiation potential of stem cells without the differentiation induction (Hirota, 2011); to compare HLA expression profiles of bone marrow-derived and adipose-derived stem cells (Purandare, 2013); and to design heart valve-shaped tri-layered collagen-based constructs for stem cell seeding and differentiation to use in heart valve tissue engineering (Tedder, 2010, 2011).
应用
blood production, hematopoietic growth and differentiation, pathways of pluripotent cell differentiation into bone, cartilage and fat, connective tissue production,supportive structure, cell production, cell proliferation, cell based therapy, tissue restoration and repair, differentiation, effects of culture conditinos, HLA expression, cytokine production, immunomodulation, clinical trials
生化/生理作用
Bone Marrow
制备说明
- 2nd passage, >500,000 cells in Basal Medium containing 10% FBS & 10% DMSO
- Can be cultured at least 10 doublings
Please refer to the HMSC Culture Protocol.
其他说明
Basal Medium containing 10% FBS & 10% DMSO
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
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