R&D  AR009 N-2 MAX Media Supplement (100X)

产品编号 AR009| rndsystems

N-2 MAX Media Supplement (100X)

产品介绍

Product Details

Kit Summary

For culturing neurons, neural progenitors, and stem cells.

Why Culture Neurons under Fully Defined Conditions?

• Serum-free, defined media are routinely used as an alternative to standard serum-containing media in order to reduce unwanted experimental variability. See Details

N-2 MAX Media Supplement Components

• Supplied as a 100X concentrate in water, this media supplement contains the following high quality factors to support neural cell culture: See Details

Precautions

• This product contains human transferrin. This transferrin was tested at the donor level using an FDA licensed method and found to be non-reactive for anti-HIV-1/2 and Hepatitis B surface antigen. As no testing can offer complete assurance of freedom from infectious agents, these reagents should be handled as if capable of transmitting infection.
• Data Examples
• Neural Progenitor Cells Expanded with N-2 Plus Media Supplement Express Nestin and SOX2. Rat Cortical Stem Cells (Catalog # NSC001) were cultured for 7 days in media supplemented with 1X N-2 MAX Media Supplement (Catalog # AR009) and 20 ng/mL of Recombinant Human FGF basic (Catalog #233-FB). The cells were stained with a PE-conjugated Mouse Anti-Human Nestin Monoclonal Antibody (Catalog # IC1259P; red histogram), a PE-conjugated Mouse Anti-Human/Mouse SOX2 Monoclonal Antibody (Catalog # IC2018P; green histogram), or a PE-conjugated Mouse IgG_2A Isotype Control (Catalog # IC003P; open histogram). Under these conditions, cells were shown to express high levels of Nestin and SOX2, two established markers of neural multipotency.
• Verification of Neural Progenitor Cell Multipotency Following Expansion with N-2 MAX Media Supplement. Rat Cortical Stem Cells (Catalog # NSC001) were grown and differentiated for 7 daysin vitro in media supplemented with N-2 MAX Media Supplement (Catalog # AR009). Markers of lineage differentiation were detected using a Mouse Anti-Neuron-specific beta-III Tubulin Monoclonal (clone TuJ-1) Antibody (Catalog #MAB1195), followed by a NorthernLights^™ (NL)557-conjugated Donkey Anti-Mouse Secondary Antibody (Catalog # NL007; red), a Sheep Anti-Human GFAP Antigen Affinity-purified Polyclonal Antibody (Catalog #AF2594), followed by a NL557-conjugated Donkey Anti-Sheep Secondary Antibody (Catalog # NL010; red), and a Mouse Anti-Human/Mouse/Rat/Chicken Oligodendrocyte Marker O4 Monoclonal Antibody (Catalog # MAB1326), followed by a NL 557-conjugated Goat Anti-Mouse Secondary Antibody (Catalog # NL019; red). The nuclei were counterstained with DAPI (blue). View our protocol forFluorescent ICC Staining of Stem Cells on Coverslips.

Preparation and Storage

Stability & Storage

Store the unopened product at -20 to -70 °C. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Do not use past expiration date.

Background: Mesenchymal Stem Cells

The term 'mesenchymal stem cells' (MSCs) is most commonly used to describe multipotent self-renewing cells that can be differentiated in vitro to generate adipocytes, chondrocytes, and osteoblasts. However, because these biological properties and hierarchical relationships remain to be clearly demonstrated in vivo, the term 'multipotent mesenchymal stromal cells' is often used to distinguish cultured cells from their in vivo precursors. Originally discovered in mouse bone marrow, multipotent mesenchymal stromal cells cultured from a variety of species and tissue types, have been shown to differentiate into progeny of additional lineages including, cardiomyocytes, endothelial cells, hepatocytes, and neural cells. Again, the physiological relevance of these findings remains to be determined.

公司简介

R&D Systems作为全球免疫学和细胞生物学产品的领跑者，1976年创立于美国明尼苏达州。其母公司Bio-Techne（原Techne公司）于1983年在美国NASDAQ上市。

目前，R&D Systems拥有近30,000种产品，95%以上由自己研发生产。其产品包括细胞因子、ELISA试剂盒、生长因子、趋化因子、抗体、Animal-Free™蛋白、Luminex 液相芯片、多因子检测固相芯片、流式细胞分析与细胞筛选、干细胞及细胞培养等；覆盖肿瘤、发育、糖生物、内分泌、免疫、神经学、蛋白酶、信号传导等学科研究领域；且每年有近2,000种新产品不断问世，以满足不同科研工作者的研究需要。

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