Mouse Oncostatin-M,OSM ELISA KIT

Code CSB-E04697m
Size 96T,5×96T,10×96T
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Product Details

Target Name
oncostatin M
Alternative Names
Osm ELISA Kit; Oncostatin-M ELISA Kit; OSM ELISA Kit
Uniprot No.
Mus musculus (Mouse)
Sample Types
serum, plasma, cell culture supernates, tissue homogenates
Detection Range
3.12 pg/mL-200 pg/mL
0.78 pg/mL
Assay Time
Sample Volume
Detection Wavelength
450 nm
Research Area
Assay Principle
Intra-assay Precision (Precision within an assay): CV%<8%
Three samples of known concentration were tested twenty times on one plate to assess.
Inter-assay Precision (Precision between assays): CV%<10%
Three samples of known concentration were tested in twenty assays to assess.
To assess the linearity of the assay, samples were spiked with high concentrations of mouse OSM in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
1:20Average %93
Range %88-97
1:40Average %84
Range %80-88
1:80Average %95
Range %90-100
1:160Average %98
Range %94-105
The recovery of mouse OSM spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.
Sample TypeAverage % RecoveryRange
Serum (n=5) 9185-96
EDTA plasma (n=4)104100-108
Typical Data
These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
pg/ml OD1OD2AverageCorrected
2002.234 2.151 2.193 2.014
1001.715 1.807 1.761 1.582
501.234 1.154 1.194 1.015
250.779 0.813 0.796 0.617
12.50.587 0.612 0.600 0.421
6.250.353 0.345 0.349 0.170
3.120.271 0.257 0.264 0.085
00.183 0.175 0.179
and FAQs
Store at 2-8°C. Please refer to protocol.
Lead Time
3-5 working days after you place the order, and it takes another 3-5 days for delivery via DHL or FedEx

This Mouse OSM ELISA Kit was designed for the quantitative measurement of Mouse OSM protein in serum, plasma, cell culture supernates, tissue homogenates. It is a Sandwich ELISA kit, its detection range is 3.12 pg/mL-200 pg/mL and the sensitivity is 0.78 pg/mL.

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Target Background

(From Uniprot)
Growth regulator. Inhibits the proliferation of a number of tumor cell lines. It regulates cytokine production, including IL-6, G-CSF and GM-CSF from endothelial cells. Uses only type II OSM receptor (heterodimers composed of OSMR and IL6ST). Involved in the maturation of fetal hepatocytes, thereby promoting liver development and regeneration.
Gene References into Functions
  1. Oncostatin M is a secreted niche factor responsible for quiescence induction PMID: 29670077
  2. data revealed that OSM alleviated postinfarction cardiac remodeling and dysfunction by enhancing cardiomyocyte autophagy. OSM holds promise as a therapeutic target in treating HF after MI through Obeta receptor by inhibiting Mst1 phosphorylation. PMID: 27825852
  3. TRAF5 is crucially involved in OSM-mediated lung inflammation probably by inducing lung stromal/fibroblast cell activation. PMID: 29596835
  4. OSM mitigated the proliferation of Th17 cells and decreased the expression of IL-17 and IL-21; it promoted the activation of suppressor of cytokine signaling 3 (SOCS3), STAT3, and STAT5; observations suggest that OSM can inhibit Th17 differentiation by reciprocally controlling SOCS3, STAT3, and STAT5 PMID: 28093521
  5. In an animal model of anti-TNF-resistant intestinal inflammation, genetic deletion or pharmacological blockade of OSM significantly attenuates colitis. PMID: 28368383
  6. these results support the proinflammatory role of OSM when it is overexpressed in the skin. However, OSM expression was not required in the murine model of psoriasis induced by topical application of imiquimod, as demonstrated by the inflammatory phenotype of OSM-deficient mice or wild-type mice treated with anti-OSM antibodies. PMID: 27122058
  7. Loss of Oncostatin M Signaling in Adipocytes Induces Insulin Resistance and Adipose Tissue Inflammation in Vivo. PMID: 27325693
  8. mechanism of OSM-induced cardiomyocyte dedifferentiation is associated with B-Raf/Mek/Erk signaling pathway through the OSM receptor Obeta PMID: 26837420
  9. Oncostatin M and interleukin-31: Cytokines, receptors, signal transduction and physiology. PMID: 26198770
  10. OSM plays multiple critical roles in the maintenance and development of the hematopoietic microenvironment in the bone marrow at a steady state as well as after injury. PMID: 25551451
  11. OSM treatment preserved cardiac function, inhibited apoptosis and fibrosis, and stimulated angiogenesis via upregulating VEGF and bFGF in infarct border zone of ischemic myocardium, indicating that OSM could be a novel therapeutic target for MI. PMID: 26146616
  12. OSM-induced osteogenesis and upregulation of osteogenic gene products require activity of PKCdelta. PMID: 25634144
  13. administration of Fstl1 induced airway remodeling and increased OSM, whereas administration of an anti-OSM Ab blocked the effect of Fstl1 on inducing airway remodeling, eosinophilic airway inflammation PMID: 26355153
  14. A novel role for OSM during pneumonia as an important signal to epithelial cells for chemokine induction mediating neutrophil recruitment. PMID: 25692402
  15. These results suggest that mOSM, a product of macrophages, sustains intramembranous bone formation by signaling through Osmr and Stat3, acting on the recruitment, proliferation, and/or osteoblast differentiation of endosteal mesenchymal progenitor cells. PMID: 25559270
  16. In astrocytes but not microglia, phosphorylation of STAT1 and STAT3 occurred in response to OSM, whereas both microglia and astrocytes responded to hyper-IL-6 (IL-6 linked to the soluble IL-6 receptor). PMID: 25103368
  17. Following spinal cord injury, OSM is produced at the lesion site, where it protects the CNS from further damage and promotes recovery PMID: 24996996
  18. OSM promotes tumour growth, and does so through altering the local lung environment with accumulation of M2 macrophages. PMID: 24976180
  19. these results support the ability of OSM to induce B cell activation and iBALT formation independently of IL-6 and highlight a role for IL-6 downstream of OSM in the induction of pulmonary inflammation. PMID: 23797667
  20. Oncostatin M induces thermal hypersensitivity by directly sensitizing nociceptors via OSMR-gp130 receptor mediated potentiation of TRPV1. PMID: 22196363
  21. Oncostatin M (OSM), a cytokine of the IL-6 family, was identified as a major coupling factor produced by activated circulating CD14+ or bone marrow CD11b+ monocytes/macrophages. PMID: 22267310
  22. Oncostatin M (OSM) is a major mediator of cardiomyocyte dedifferentiation and remodeling during acute myocardial infarction (MI) and in chronic dilated cardiomyopathy (DCM). PMID: 22056139
  23. we show that Oncostatin M (Osm) and its receptor, OsmRbeta, are both expressed in the subventricular zone and that Osm directly inhibits the proliferation of adult neural precursor cells PMID: 21671408
  24. OSM is expressed in atherosclerotic lesions and may contribute to the progression of atherosclerosis by promoting SMC proliferation, migration and extracellular matrix protein synthesis through the STAT pathway PMID: 21376322
  25. Loss of oncostatin M is associated with chondrosarcoma. PMID: 21344373
  26. Overexpression of mouse oncostatin M induces STAT6-dependent pulmonary eosinophilia, mucous/goblet cell hyperplasia, and airway hyperresponsiveness but STAT6-independent mechanisms of lung tissue extracellular matrix accumulation. PMID: 21160052
  27. These studies are the first to demonstrate the proinflammatory effects of OSM in microglia, and also identify IL-27 as a novel inhibitor of inflammatory processes in these cells. PMID: 20468050
  28. Findings provide evidence that the inflammatory cytokine oncostatin M is involved in modulation of the Ang-Tie system by increasing Ang2 expression in human endothelial cells in vitro, and in murine hearts and human hearts in vivo. PMID: 20088942
  29. these results indicate that OSM may play a role in innate immunity and in acquired immunity by enhancing DCs maturation and promoting Th1 immune responses. PMID: 20206608
  30. Oncostatin M (OSM) is produced by osteoblasts and osteocytes in mouse bone and that it has distinct effects when acting through 2 different receptors. PMID: 20051625
  31. Results show that oncostatin M favors bone apposition at periosteal sites instead of resorption in vivo, and this effect was not dependent on or inhibited by IL-6. PMID: 12000725
  32. role for OSM in inflammatory responses that can modulate steady-state ECM deposition in Balb/C mice PMID: 12023835
  33. Th1 cells regulate hematopoietic progenitor cell homeostasis by production of oncostatin M PMID: 12121663
  34. Oncostatin M stimulates (45)Ca release and enhances mRNA expression of receptor activator of NF-kappa B ligand (RANKL) and osteoprotegerin in neonatal calvarial bone cultures, but has no effect on the expression of RANK. PMID: 12218157
  35. oncostatin m mRNA-positive cells were found in hematopoietic organs during development PMID: 12412016
  36. OSM induces eotaxin expression in mouse fibroblasts at the protein and mRNA level, and adenovirus vector-encoding OSM induces eosinophilia in the lung in vivo following intranasal administration. PMID: 12496442
  37. Mouse OSM upregulates MMP-9 expression in rat smooth muscle cells through the MEK-ERK but not STAT3 pathway. PMID: 12615664
  38. Oncostatin M (OM) transforms the lymph node (LN) into a "super lymphoid organ" with 2 striking features: massive thymus-independent T-cell development and major expansion of the memory T-cell pool. PMID: 12702501
  39. Oncostatin M[OSM]-deficient mice displayed significantly reduced noxious responses in models of acute pain. Thus, OSM plays an essential role in the development of a subtype of nociceptive neurons in the dorsal root ganglia PMID: 14985435
  40. OSM causes a loss of cell-cell and cell-substratum adhesion ending in cell detachment from monolayer culture. OSM induces the expression of Cox-2. It could contribute to the development of a metastatic phenotype in vivo. PMID: 15168734
  41. Oncostatin M in combination with either IL-1 or tumour necrosis factor alpha represents cytokine combinations that promote bone destruction. PMID: 15642143
  42. Oncostatin M uniquely induces significant release of keratinocyte-derived chemokine (KC) and lipopolysaccharide-induced chemokine (LIX) in mouse cardiac fibroblasts. PMID: 16452159
  43. role of OSM in regulation of VCAM-1 expression, and STAT6 tyrosine 641 phosphorylation in murine fibroblasts PMID: 16547273
  44. OSM arrests skeletal muscle cell growth at the G1/S checkpoint and this response occurs by an ubiquitin/proteasome-dependent cyclin D1 protein reduction which is regulated by STAT3 PMID: 17976956
  45. Both LY294002 and PD98059 attenuated Oncostatin M-induced phosphorylation of ERK1/2 MAP kinase and also reduced binding of an AP-1 responsive promoter element, a transcriptional complex known to be MAPK-sensitive. PMID: 18372159
  46. A dual role for oncostatin M signaling in the differentiation and death of mammary epithelial cells in vivo. PMID: 18927239
  47. The expression of SCGB3A1 and SCGB3A2 are bidirectionally regulated by oncostatin M (OSM) when examined in a mouse transformed Clara cell line. PMID: 18978304
  48. Results suggest that OSM plays a key role in the prevention of autoimmune disease by regulating the clearance of apoptotic thymocytes. PMID: 19384873

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Subcellular Location
Protein Families
LIF/OSM family
Database Links
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