Mouse Oncostatin M (OSM) Quantikine ELISA Kit | mOSM basic Qkit

掲載日情報:2016/08/18 現在Webページ番号:111354

R&D Systems製のMouse Oncostatin M (OSM)を測定するELISAキットです。
本製品は研究用です。研究用以外には使用できません。

[在庫・価格 :2024年06月08日 00時01分現在]

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Mouse Oncostatin M (OSM) Quantikine ELISA Kit
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説明文
感度:4.7 pg/mL,測定範囲:7.81 - 500 pg/mL,測定試料:Cell Culture Supernates (50 uL), Serum (50 uL), EDTA Plasma (50 uL), Heparin Plasma (50 uL),種交差性:Mouse,測定波長:450 nm,検出方法:呈色,アッセイ法:Solid Phase Sandwich ELISA,アッセイ数:96 well,測定時間:4.5 hours,測定因子:Oncostatin M/OSM
別名:MGC20461
Genbank No: 5008
法規制等
保存条件 4℃ 法規備考
掲載カタログ

製品記事 Quantikine Mouse Oncostatin M (OSM) ELISA Kit
Fluorochrome-Conjugated Human Arginase 1 Monoclonal Antibodies
ELISA Kit製品に関するFAQ(R&D Systems)
関連記事 R&D Systems Quantikine ELISA Kit/DuoSet Kit特集

[在庫・価格 :2024年06月08日 00時01分現在]

※ 表示されている納期は弊社に在庫が無く、取り寄せた場合の納期目安となります。

Mouse Oncostatin M (OSM) Quantikine ELISA Kit

文献数: 0

説明文 感度:4.7 pg/mL,測定範囲:7.81 - 500 pg/mL,測定試料:Cell Culture Supernates (50 uL), Serum (50 uL), EDTA Plasma (50 uL), Heparin Plasma (50 uL),種交差性:Mouse,測定波長:450 nm,検出方法:呈色,アッセイ法:Solid Phase Sandwich ELISA,アッセイ数:96 well,測定時間:4.5 hours,測定因子:Oncostatin M/OSM
別名:MGC20461
Genbank No: 5008
法規制等
保存条件 4℃ 法規備考
掲載カタログ

製品記事 Quantikine Mouse Oncostatin M (OSM) ELISA Kit
Fluorochrome-Conjugated Human Arginase 1 Monoclonal Antibodies
ELISA Kit製品に関するFAQ(R&D Systems)
関連記事 R&D Systems Quantikine ELISA Kit/DuoSet Kit特集

Product Details

Assay Type
Solid Phase Sandwich ELISA
Format
96-well strip plate
Assay Length
4.5 hours
Sample Type & Volume Required Per Well
Cell Culture Supernates (50 µL), Serum (50 µL), EDTA Plasma (50 µL), Heparin Plasma (50 µL)

Sensitivity
4.7 pg/mL
Assay Range
7.81 - 500 pg/mL (Serum, Heparin Plasma, Cell Culture Supernates, EDTA Plasma)
Specificity
Natural and recombinant mouse OSM.
Interference
No significant interference observed with available related molecules.

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Product Summary

The Quantikine Mouse Oncostatin M (OSM) Immunoassay is a 4.5 hour solid phase ELISA designed to measure mouse OSM levels in cell culture supernates, serum, and plasma. It contains E. coli-expressed recombinant mouse OSM and antibodies raised against the recombinant factor. This immunoassay has been shown to quantitate the recombinant mouse OSM accurately. Results obtained using natural mouse OSM showed dose-response curves that were parallel to the standard curves obtained using the recombinant kit standards. These results indicate that this kit can be used to determine relative mass values for natural mouse OSM.

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Precision

Intra-Assay Precision (Precision within an assay)
Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays)
Three samples of known concentration were tested in twenty separate assays to assess inter-assay precision. Assays were performed by at least three technicians using two lots of components.

Cell Culture Supernates, Serum, EDTA Plasma, Heparin Plasma

Intra-Assay Precision Inter-Assay Precision
Sample 1 2 3 1 2 3
n 20 20 20 20 20 20
Mean 36.7 62.1 127 36.5 65.3 135
Standard Deviation 2.36 1.32 3.64 4.53 6.2 9.2
CV% 6.4 2.1 2.9 12.4 9.5 6.8

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Recovery

The recovery of mouse OSM spiked to three levels throughout the range of the assay in various matrices was evaluated.

Sample Type Average % Recovery Range %
Cell Culture Media (n=4) 97 92-103
Serum (n=4) 100 95-109
EDTA Plasma (n=4) 95 92-100
Heparin Plasma (n=4) 99 94-106

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Linearity

To assess the linearity of the assay, samples spiked with high concentrations of mouse OSM were serially diluted with Calibrator Diluent to produce samples with values within the dynamic range of the assay.

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Additional Infomation

Molecule Information
Oncostatin M/OSM
Aliases
undefined
Entrez Gene IDs
5008 (Human); 18413 (Mouse)
Background
Oncostatin M and Receptor
Oncostatin M (OSM) is a cytokine originally isolated from medium conditioned by PMA-treated U-937 human histiocytic leukemia cells based on its ability to inhibit growth of A375 melanoma cells. The human OSM cDNA encodes a 252 amino acid pre-pro-OSM polypeptide with a 25 residue hydrophobic signal peptide and a hydrophilic C-terminal domain that are proteolytically processed to generate the 196 residue mature form of OSM. Although both mature and pro-OSM are equally active in radio-receptor assays, the mature OSM is 5- to 60-fold more active in growth inhibition assays. Thus, proteolytic processing of the pro-OSM peptide may be important in regulating the in vivo activities of OSM. OSM initiates its biological activities by binding to specific cell surface receptors. The gp130, a signal transducing component (beta subunit) of the IL-6, LIF and CNTF receptor complexes, was identified as a low-affinity OSM receptor that does not transduce OSM signals. The low affinity LIF receptor (LIF R, a gp130-related protein) has now been identified to be a component of a high-affinity OSM receptor that will transduce OSM signals. Since OSM is also active on cells that do not express LIF R, a specific OSM receptor that does not involve LIF R must also exist. Besides its growth inhibitory activities on human A375 melanoma and mouse M1 myeloid leukemic cells, as well as on other solid tumor cells, OSM also has growth stimulatory activities on normal fibroblasts, AIDS-Kaposi's sarcoma cells, and a human erythroleukemia cell line, TF-1. 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.Human Oncostatin M (OSM) signals through two types of human OSM receptor complexes: the type I complex comprising the leukemia inhibitory factor receptor beta (LIF R beta) and gp130 and the type II complex made up of OSM receptor beta (OSM R beta) and gp130. In contrast, mouse OSM signals only through the mouse OSM R beta and gp130 complex. Human and mouse OSM R beta are 55% identical at the amino acid sequence level.

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Citations

Citations of cell biology reagents in peer reviewed literature can be used as a direct measure of product quality. They can also provide crucial insightinto their use under specialized or unique experimental conditions. Because of the importance published citations have to researchers, R&D Systems personnelmanually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but alsoprovides information about sample types, species, and experimental conditions.

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