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花生四烯酸(AA)酶联免疫吸附检测试剂盒

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ELK11240

规格：	价格：
48T	￥2240.00
96T	￥3200.00

下载说明 ①

Overview

Product name:	AA(Arachidonic Acid) ELISA Kit
Reactivity:	General
Alternative Names:	ARA
Assay Type:	Competitive Inhibition
Sensitivity:	0.57 ng/mL
Standard:	100 ng/mL
Detection Range:	1.57-100 ng/mL
Sample type:	Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay length:	2h
Research Area:	Signal transduction;Metabolic pathway;Endocrinology;Neuro science;Hormone metabolism;Bone metabolism;
Test principle:	This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with AA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to AA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of AA in the samples is then determined by comparing the OD of the samples to the standard curve.

标准曲线

Concentration (ng/mL)	OD	Corrected OD
100.00	0.185
50.00	0.336
25.00	0.557
12.50	0.899
6.25	1.236
3.13	1.537
1.57	1.733
0.00	2.213

精密度

Intra-assay Precision (Precision within an assay)：CV%<8%

Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Inter-assay Precision (Precision between assays)：CV%<10%

Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.

回收率

Matrices listed below were spiked with certain level of recombinant AA and the recovery rates were calculated by comparing the measured value to the expected amount of AA in samples.

Matrix	Recovery range	Average
serum(n=5)	90-105%	97%
EDTA plasma(n=5)	88-102%	95%
Heparin plasma(n=5)	94-107%	100%

线性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of AA and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.