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SCM122 Sigma-Aldrich

AdipoMAX Differentiation Medium

Synonym: MSC adipocyte media, adipocyte differentiation media, adipogenesis media

  •  NACRES NA.75

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Properties

Related Categories Cell Analysis, Cell Biology, Cell Culture, Mesenchymal Stem Cells, Specialty Media Systems,
shipped in   dry ice
storage temp.   −20°C

Description

General description

Mesenchymal stem cells (MSCs) are adult stem cells, which have the capacity for multi-lineage differentiation, giving rise to a variety of mesenchymal phenotypes such as osteoblasts (bone), adipocytes (fat), and chondrocytes (cartilage). Obesity related diseases pose significant health challenges to many industrialized nations. Many metabolic disorders associated with cardiovascular diseases, such as diabetes and atherosclerosis, are directly linked to the increased production and size of adipose cells.
AdipoMAX Differentiation Media is a ready-to-use mesenchymal stem cell adipogenesis differentiation media. AdipoMAX produces cells with elevated levels of lipids, analyzed by Oil-Red-O staining, after 3 weeks of differentiation compared to other adipogenesis differentiation media. AdipoMAX is an excellent research tool to study adipocyte differentiation, adipogenesis and adipocyte related metabolic diseases.

Other Notes

AdipoMAX Differentiation Medium consists of a 100 mL basal medium component and a 10 mL dilution factor component, both of which can be stored at -20°C until ready to use.

Before use, thaw both materials and combine the dilution factor into the basal medium. The complete medium can be stored at 2-8°C for up to 3 weeks.

Safety & Documentation

Safety Information

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NONH for all modes of transport

Documents

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Protocols & Articles

Articles

Mesenchymal Stem Cell FAQs

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Protocols

Mesenchymal Stem Cell Culture Protocols

Introduction Methods   Isolation of Mesenchymal Stem Cells   Expansion of Human Mesenchymal Stem Cells     Preparation of Coated Plates     Thawing of Mesenchymal Stem Cells     Expansion of Mesenchy...
Keywords: Cell disruption, Clinical, Culture media, Gene expression, Immunocytochemistry, Stem cell biology

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