Human Cyr61/CCN1 Quantikine ELISA Kit | hCyr61 Qkit

掲載日情報:2016/08/18 現在Webページ番号:111071

R&D Systems製のHuman Cyr61/CCN1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05月22日 00時00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。
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Human Cyr61/CCN1 Quantikine ELISA Kit
10日程度 ※ 表示されている納期は弊社に在庫がなく、取り寄せた場合の目安納期となります。 3
説明文
種交差性:Human,感度:3.8 pg/mL,測定範囲:39.10 - 2500 pg/mL,測定試料:Cell Culture Supernates (50 uL), Serum (50 uL), EDTA Plasma (50 uL), Saliva (50 uL), Human Milk (10 uL),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,別売品コントロール:#QC73,測定時間:4.5 hours,測定因子:Cyr61/CCN1
別名:CCN family member 1
Genbank No: 3491
法規制等
保存条件 4℃ 法規備考
掲載カタログ

製品記事 Quantikine Human Cyr61 ELISA Kit
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05月22日 00時00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。

Human Cyr61/CCN1 Quantikine ELISA Kit

文献数: 3

説明文 種交差性:Human,感度:3.8 pg/mL,測定範囲:39.10 - 2500 pg/mL,測定試料:Cell Culture Supernates (50 uL), Serum (50 uL), EDTA Plasma (50 uL), Saliva (50 uL), Human Milk (10 uL),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,別売品コントロール:#QC73,測定時間:4.5 hours,測定因子:Cyr61/CCN1
別名:CCN family member 1
Genbank No: 3491
法規制等
保存条件 4℃ 法規備考
掲載カタログ

製品記事 Quantikine Human Cyr61 ELISA Kit
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), Saliva (50 µL), Human Milk (10 µL)

Sensitivity
3.8 pg/mL
Assay Range
39.1 - 2,500 pg/mL (Serum, Saliva, Cell Culture Supernates, Human Milk, EDTA Plasma)
Specificity
Natural and recombinant human Cyr61
Interference
No significant interference observed with available related molecules.

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Product Summary

The Quantikine Human Cyr61/CCN1 Immunoassay is a 4.5 hour solid-phase ELISA designed to measure human Cyr61 in cell culture supernates, serum, plasma, saliva, and human milk. It contains CHO cell-expressed recombinant human Cyr61 and has been shown to accurately quantitate the recombinant factor. Results obtained using natural human Cyr61 showed linear curves that were parallel to the standard curves obtained using the Quantikine kit standards. These results indicate that this kit can be used to determine relative mass values for naturally occurring Cyr61.

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Precision

Intra-Assay Precision (Precision within an assay)
Three samples of known concentration were tested on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays)
Three samples of known concentration were tested in separate assays to assess inter-assay precision.

Cell Culture Supernates, Serum, EDTA Plasma, Saliva, Human Milk

Intra-Assay Precision Inter-Assay Precision
Sample 1 2 3 1 2 3
n 20 20 20 20 20 20
Mean 256 721 1,442 249 712 1,445
Standard Deviation 5.94 14.2 33.5 15.9 35 73.3
CV% 2.3 2 2.3 6.4 4.9 5.1

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Recovery

The recovery of Cyr61 spiked to levels throughout the range of the assay in various matrices was evaluated.

Sample Type Average % Recovery Range %
Cell Culture Media (n=4) 107 98-117
Serum (n=4) 101 95-113
EDTA Plasma (n=4) 98 91-104

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Linearity

To assess the linearity of the assay, samples containing and/or spiked with high concentrations of Cyr61 were diluted with Calibrator Diluent to produce samples with values within the dynamic range of the assay.

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Additional Infomation

Molecule Information
Cyr61/CCN1
Aliases
CCN1; GIG1; IGFBP-10
Entrez Gene IDs
3491 (Human); 16007 (Mouse); 83476 (Rat)
Background
Cyr61
Cyr61, also known as IGFBP-10 and CCN1, is a 50 kDa matricellular glycoprotein that regulates the growth and adhesion of vascular endothelial cells, fibroblasts, and monocytes. Cyr61 induces VEGF upregulation, angiogenesis, and tumorigenesis through interactions with integrins alpha V beta 3, alpha V beta 5, alpha M beta 2, and alpha 6 beta 1. Cyr61 is cleaved by plasmin within its VWF domain which generates an N-terminal fragment that is not associated with the matrix but retains the ability to induce endothelial cell migration.

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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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