Rat IL-1 alpha/IL-1F1 Quantikine ELISA Kit | rIL-1a Qkit

掲載日情報:2016/08/18 現在Webページ番号:111399

R&D Systems製のRat IL-1 alpha/IL-1F1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 :2025年04月27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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IL-1α, Rat, ELISA Kit, Quantikine (96 well) <IL-1F1, 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。 5
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説明文
測定範囲:15.6-1,000 pg/mL,感度:4.12 pg/mL,測定試料:Serum, Plasma, Cell Culture Supernatant,種交差性:Rat,検出方法:呈色,測定波長:450 nm,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:IL-1 alpha, IL-1F1
別名:Hematopoietin-1
Genbank No: 3552
法規制等 医薬用外毒物
保存条件 4℃ 法規備考
掲載カタログ ニュース2018年7月1日号 p.11
ニュース2019年8月15日号 p.15

製品記事 がん幹細胞関連因子測定用 Quantikine 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
Quantikine ELISA Kit

[在庫・価格 :2025年04月27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。

IL-1α, Rat, ELISA Kit, Quantikine (96 well) <IL-1F1, ELISA Kit>

文献数: 5

説明文 測定範囲:15.6-1,000 pg/mL,感度:4.12 pg/mL,測定試料:Serum, Plasma, Cell Culture Supernatant,種交差性:Rat,検出方法:呈色,測定波長:450 nm,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:IL-1 alpha, IL-1F1
別名:Hematopoietin-1
Genbank No: 3552
法規制等 医薬用外毒物
保存条件 4℃ 法規備考
掲載カタログ ニュース2018年7月1日号 p.11
ニュース2019年8月15日号 p.15

製品記事 がん幹細胞関連因子測定用 Quantikine 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
Quantikine ELISA Kit

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)

Sensitivity
4.12 pg/mL
Assay Range
15.6 - 1,000 pg/mL (Serum, Cell Culture Supernates, EDTA Plasma)
Specificity
Natural and recombinant rat IL-1 alpha
Interference
Interference observed with 1 or more available related molecules.

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Product Summary

The Quantikine Rat IL-1 alpha Immunoassay is a 4.5 hour solid phase ELISA designed to measure rat IL-1 alpha levels in cell culture supernates, serum, and plasma. It contains E. coli-expressed recombinant rat IL-1 alpha and antibodies raised against the recombinant factor. This immunoassay has been shown to quantitate the recombinant rat IL-1 alpha accurately. Results obtained using natural rat IL-1 alpha showed dose curves that were parallel to the standard curves obtained using the recombinant Quantikine kit standards. These results indicate that this kit can be used to determine relative mass values for natural rat IL-1 alpha.

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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

Intra-Assay Precision Inter-Assay Precision
Sample 1 2 3 1 2 3
n 20 20 20 20 20 20
Mean 54 134 417 54 130 449
Standard Deviation 3.6 6.3 16.5 5 9.5 29.7
CV% 6.7 4.7 4 9.3 7.3 6.6

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Recovery

The recovery of rat IL-1 alpha spiked to three levels throughout the range of the assay in various matrices was evaluated.

Sample Type Average % Recovery Range %
Serum (n=4) 92 85-99
Cell Culture Supernates (n=4) 104 100-111
EDTA Plasma (n=5) 98 89-112

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Linearity

To assess the linearity of the assay, samples spiked with rat IL-1 alpha in each matrix were diluted with Calibrator Diluent and then assayed.

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Additional Infomation

Molecule Information
IL-1 alpha/IL-1F1
Aliases
IL1A; IL-1F1
Entrez Gene IDs
3552 (Human); 16175 (Mouse); 24493 (Rat); 397094 (Porcine)
Background
IL-1 alpha/IL-1F1
Interleukin-1 (IL-1) is a name that designates two proteins, IL-1 alpha and IL-1 beta, which are the products of distinct genes, but which show approximately 25% amino acid sequence identity and which recognize the same cell surface receptors. Although IL-1 production is generally considered to be a consequence of inflammation, recent evidence suggests that IL-1 is also temporarily upregulated during bone formation and the menstrual cycle and can be induced in response to nervous system stimulation. In response to classic stimuli produced by inflammatory agents, infections or microbial endotoxins, a dramatic increase in the production of IL-1 by macrophages and various other cells is seen. Cells in particular known to produce IL-1 include osteoblasts, monocytes, macrophages, keratinocytes, Kupffer cells, hepatocytes, thymic and salivary gland epithelium, Schwann cells, fibroblasts and glia (oligodendroglia, astrocytes and microglia).IL-1 alpha and IL-1 beta are both synthesized as 31 kDa precursors that are subsequently cleaved into proteins with molecular weights of approximately 17,000. Neither precursor contains a typical hydrophobic signal peptide sequence and most of the precursor form of IL-1 alpha remains in the cytosol of cells, although there is evidence for a membrane-bound form of the precursor form of IL-1 alpha. The IL-1 alpha precursor reportedly shows full biological activity in the EL 4 assay. Among various species, the amino acid sequence of mature IL-1 alpha is conserved 60% to 70% and human IL-1 has been found to be biologically active on murine cell lines. Both forms of IL-1 bind to the same receptors, designated type I and type II. Recent evidence suggests that only the type I receptor is capable of signal transduction and that the type II receptor may function as a decoy, binding IL-1 and thus preventing binding of IL-1 to the type I receptor.

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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.

Regulation of interleukin 1alpha, activin and inhibin by lipopolysaccharide in Sertoli cells from prepubertal rats.
Okuma Y, Saito K, Winnall WR
Mol. Cell. Endocrinol. 2009 307:169-75
Species: Rat
Sample Type: Cell Culture Supernates


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