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OSM(209aa) Protein, Human

OSM(209aa) Protein, Human

Catalog Number: UA040051 Reactivity: Human Conjugation: Unconjugated Brand: UA BIOSCIENCE
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Regular price $112 USD
Regular price Sale price $112 USD
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Product Details

Product Specification


Species Human
Synonyms OSM, Oncostatin M, MGC20461, OncoM
Accession P13725
Amino Acid Sequence Ala26-Arg234
Expression System E.coli
Molecular Weight 24kDa
Purity >95% by SDS-PAGE
Endotoxin <1EU/μg
Conjugation Unconjugated
Tag No Tag
Physical Appearance Lyophilized Powder
Storage Buffer 20mM Tris, 150mM NaCl, pH8.0, 1mM TCEP
Reconstitution Reconstitute at 0.1-1 mg/ml according to the size in ultrapure water after rapid centrifugation.
Stability & Storage

12 months from date of receipt, -20 to -70 °C as supplied; 

6 months, -20 to -70 °C under sterile conditions after reconstitution; 

1 week, 2 to 8 °C under sterile conditions after reconstitution; 

Please avoid repeated freeze-thaw cycles.

Reference

1、Tanaka M. et al. (2003) Oncostatin M, a multifunctional cytokine. Rev Physiol Biochem Pharmacol. Reviews of Physiology, Biochemistry and Pharmacology. 149: 39-52.

2、Auguste P, et al. (1997) Signaling of type II oncostatin M receptor. J Biol Chem. 272(25): 15760-15764.

Background

Oncostatin M (OSM) was initially identified as a polypeptide cytokine which inhibited the in vitro growth of cells from melanoma and other solid tumors. OSM shows significant similarities in primary amino acid sequence and predicted secondary structure to leukemia inhibitory factor (LIF), ciliary neurotrophic factor (CNTF), granulocyte colony-stimulating factor (G-CSF), interleukin 6 (IL-6), and interleukin 11 (IL-11). The antiproliferative activity of oncostatin M for some cell lines is synergised by TGF-beta and IFN-gamma. It promotes the growth of human fibroblasts, vascular smooth muscle cells, and some normal cell lines. Other OSM-mediated activities reported to date include: stimulation of plasminogen activator activity in cultured bovine aortic endothelial cells; regulation of IL-6 expression in human endothelial cells; and stimulation of LDL uptake and up-regulation of cell surface LDL receptors in HepG2 cells.

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Bioactivity

Measured by a cell proliferation assay using TF-1 cells, The EC50 for this effect is less than 1ng/ml.

SDS-PAGE

1μg (R: reducing condition, N: non-reducing condition).

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