Human IL-12 p70 Recombinant Protein

Also known as: Interleukin-12, IL12, p70

RUO: For Research Use Only. Not for use in diagnostic procedures.

SKU# 14-8129

Cat. No. Size
14-8129-62 5 ug
Please inquire about custom configurations or bulk packaging.

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Data for Human IL-12 p70 Recombinant Protein.

Description

Description: Interleukin-12 (IL-12) is a heterodimeric 70 kD (p70) cytokine composed of two covalently linked, glycosylated chains, 40kD (p40) and 35-kD (p35). IL-12 is mainly produced by monocytes, macrophages, and dendritic cells in response to bacterial products such as lipopolysaccharides (LPS), to intracellular pathogens or upon interaction with activated T cells. IL-12 was originally discovered because of its ability to induce interferon-gamma (IFN-γ) production, cell proliferation, and cytotoxicity mediated by natural killer cells and T cells. It is now established that IL-12 also plays a key role in the development of Th1 responses, leading to IFN-γ and IL-2 production. These cytokines can in turn promote T-cell responses and macrophage activation.

Details
Reactivity Human
Purity Greater than 98%, as determined by SDS-PAGE
Molecular Mass The heterodimeric, p40, amino acids ile 23-ser 328, cystine linked to p35, amino acids arg 57-ser 253, has a predicted molecular mass of 57,239. On non-reducing SDS-PAGE the heterodimeric cystine-linked protein migrates as a 67 kDa protein. The DTT reduce
Endotoxin Level Less than 0.01 ng/ug cytokine as determined by the LAL assay.
Reported Applications ELISA Recombinant Standard, Cytokine Bioassays
Documentation
TDS Link Download TDS
Additional Formats
Cat. No. Name Excite Emit Application Reg.
34-8129 Human IL-12 p70 Recombinant Protein Carrier-Free ELISA, FA RUO
39-8129 Human IL-12 p70 Single-Use ELISA RSG Standard ELISA RUO
Related Products
Cat. No. Name Excite Emit Application Reg.
14-8231 Mouse IL-23 Recombinant Protein ELISA, FA RUO
14-8239 Human IL-23 Recombinant Protein ELISA, FA RUO
88-7237 Human IL-23 ELISA Ready-SET-Go!® Set ELISA RUO
References

References: Isler, P., et al. 1999. Am. J. Respir. Cell Mol. Biol. 20: 270-278.