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Mesenchymal Stem Cell Osteogenic Differentiation Medium
We offer a complete Mesenchymal Stem Cell Media System including growth media, differentiation media and human mesenchymal stem cells (MSC).
We offer five MSC Differentiation Media to efficiently induce differentiation of MSC into adipogenic, chondrogenic (with and without inducers), osteogenic or neurogenic lineages, respectively.
Our Mesenchymal Stem Cell Osteogenic Differentiation Media was developed for the directed differentiation of Human Mesenchymal Stem Cells (MSC) from bone marrow, the umbilical cord matrix (Wharton's Jelly) and adipose tissue into osteogenic lineages.
Although all our media are optimized for use with primary human cells, we have received feedback from customers that this particular medium can also be used for porcine cells.
View a list of references where this medium was used with other species and cell types.

After addition of the SupplementMix or SupplementPack to our basal medium do I have to add FCS you obtain the complete growth medium. No further supplementation with serum or growth factors is required. Please note: Our media do not contain antibiotics. If you wish to use antibiotics you can add penicillin/streptomycin or gentamicin/amphotericin B at standard concentrations. Addition of antibiotics can however reduce the doubling time of the cells up to 30-40%.
The qualitative and quantitative composition of the supplements can be found on our website and in the data sheets of the specialized media. When there is no such information specified; the composition of the supplements is confidential.
Human Mesenchymal Stem Cells have retained the ability to differentiate into a variety of cell types including fat cells; chondrocytes; and osteoblasts. PromoCell supply hMSC from 3 different tissues: bone marrow (hMSC-BM; C-12974); umbilical cord matrix (hMSC-UC; C-12971); and adipose tissue (hMSC-AT; C-12977).
- MSC-BM show very good differentiation into bone cells but also into chondrocytes and fat cells when the respective Differentiation Media is used.
- MSC-UC have a high potential to differentiate into chondrocytes but only weak potential for fat or bone cell differentiation.
- In contrast; MSC-AT differentiate very well into fat and bone cells but only moderately into chondrocytes.
- Adipogenic differentiation can be identified morphologically and without any staining by the formation of intracellular lipid vesicles.
- In contrast; when MSC differentiate into bone cells; there is no significant change in morphology. It is recommended to perform Alkaline Phosphatase staining to detect osteoblastic differentiation or Alizarin Red S staining to show osteoblast mineralization.
- Chondrogenic differentiation is generally performed as spheroids in 3-D cell culture and not in 2-D monolayer culture. Staining with Alcian Blue to visualize the differentiation process is indispensable.
- Neurogenic differentiation can be detected using neuron specific markers (e.g. beta-3 tubulin; NeuN; MAP2) and by their typical neuronal morphology.








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