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人肾上腺素(EPI)酶联免疫吸附检测试剂盒

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ELK9242

规格：	价格：
48T	￥2240.00
96T	￥3200.00

下载说明 ①

Overview

Product name:	Human EPI(Epinephrine) ELISA Kit
Reactivity:	Human
Alternative Names:	Adrenaline
Assay Type:	Competitive Inhibition
Sensitivity:	9.62 pg/mL
Standard:	2000 pg/mL
Detection Range:	31.25-2000 pg/mL
Sample type:	serum, plasma, cell lysates, cell culture supernates and other biological fluids
Assay length:	2h
Research Area:	Metabolic pathway;Infection immunity;Neuro science;Hormone metabolism;
Test principle:	This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human EPI. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human EPI. 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 Human EPI in the samples is then determined by comparing the OD of the samples to the standard curve.

标准曲线

Concentration (pg/mL)	OD	Corrected OD
2000.00	0.191
1000.00	0.411
500.00	0.611
250.00	0.823
125.00	1.253
62.50	1.596
31.25	1.871
0.00	2.211

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 EPI and the recovery rates were calculated by comparing the measured value to the expected amount of EPI in samples.

Matrix	Recovery range	Average
serum(n=5)	87-95%	91%
EDTA plasma(n=5)	82-95%	88%
Heparin plasma(n=5)	78-96%	87%

线性

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