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安全信息

C-28013

Sigma-Aldrich

Mesenchymal Stem Cell Osteogenic Differentiation Medium

Ready-to-use kit including Basal Medium and SupplementMix, 100 ml

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别名:
Primary Cell Culture Media
UNSPSC代码:
12352207
NACRES:
NA.71

形式

liquid

包装

pkg of 100 ml

技术

cell culture | mammalian: suitable

运输

wet ice

一般描述

Mesenchymal Stem Cell Osteogenic Differentiation Medium (Ready-to-use)

应用

Mesenchymal Stem Cell Osteogenic Differentiation Medium was designed for the directed differentiation of mesenchymal stem cells (MSC) from bone marrow, the umbilical cord matrix (Wharton´s Jelly) and adipose tissue into osteogenic lineages. Recommended for:Human Mesenchymal Stem Cells from Bone Marrow (hMSC-BM)Human Mesenchymal Stem Cells from Umbilical Cord Matrix (hMSC-UC)Human Mesenchymal Stem Cells from Adipose Tissue (hMSC-AT)

质量

All lots of PromoCell Mesenchymal Stem Cell Media are subjected to comprehensive quality control tests using primary human mesenchymal stem cells. Each lot of MSC Differentiation Media is tested for the capacity to induce directed differentiation into the respective lineages in MSC. In addition, all lots of media have been tested for the absence of microbial contaminants (fungi, bacteria, mycoplasma).

储存及稳定性

Store the Basal Medium at 4 to 8°C in the dark and the SupplementMix at -20°C immediately after arrival. Do not freeze the Basal Medium. If stored properly, the products are stable until the expiry date stated on the label. After adding the supplements to the Basal Medium, the shelf life of the complete medium is 6 weeks at 4 to 8°C. Do not freeze the complete medium. For use, pre-warm only an aliquot of the complete medium and keep the remaining medium refrigerated at 4 to 8°C.

传代培养常规

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WGK

WGK 3

法规信息

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Elisabetta Barresi et al.
Journal of enzyme inhibition and medicinal chemistry, 36(1), 286-294 (2020-12-19)
Small-molecules acting as positive allosteric modulators (PAMs) of the A2B adenosine receptor (A2B AR) could potentially represent a novel therapeutic strategy for pathological conditions characterised by altered bone homeostasis, including osteoporosis. We investigated a library of compounds (4-13) exhibiting different

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