前列腺素H2(PGH2)酶联免疫吸附检测试剂盒-科鹿（武汉）生物科技有限责任公司

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前列腺素H2(PGH2)酶联免疫吸附检测试剂盒

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ELK10868

规格：	价格：
48T	￥2240.00
96T	￥3200.00

下载说明 ①

Overview

Product name:	PGH2(Prostaglandin H2) ELISA Kit
Reactivity:	General
Alternative Names:	PG-H2
Assay Type:	Competitive Inhibition
Sensitivity:	12.2 pg/mL
Standard:	2000 pg/mL
Detection Range:	31.25-2000 pg/mL
Sample type:	Serum, plasma and other biological fluids
Assay length:	2h
Research Area:	Metabolic pathway;Infection immunity;Endocrinology;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 PGH2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PGH2. 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 PGH2 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	0.197
1000.00	0.375
500.00	0.611
250.00	0.873
125.00	1.197
62.50	1.583
31.25	1.813
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 PGH2 and the recovery rates were calculated by comparing the measured value to the expected amount of PGH2 in samples.

Matrix	Recovery range	Average
serum(n=5)	79-93%	86%
EDTA plasma(n=5)	87-93%	90%
Heparin plasma(n=5)	81-95%	91%

线性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of PGH2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.