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前列環(huán)素(PGI2)酶聯(lián)免疫吸附檢測試劑盒

一鍵復(fù)制產(chǎn)品信息

ELK10865

規(guī)格：	價格：
48T	￥1680.00
96T	￥2400.00

下載說明 ①

Overview

Product name:	PGI2(Prostacyclin) ELISA Kit
Reactivity:	General
Alternative Names:	prostaglandin I2
Assay Type:	Competitive Inhibition
Sensitivity:	4.8 pg/mL
Standard:	1000 pg/mL
Detection Range:	15.63-1000 pg/mL
Sample type:	serum, plasma and other biological fluids
Assay length:	2h
Research Area:	Cardiovascular biology;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 PGI2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to PGI2. 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 PGI2 in the samples is then determined by comparing the OD of the samples to the standard curve.

標(biāo)準(zhǔn)曲線

Concentration (pg/mL)	OD	Corrected OD
1000.00	0.211
500.00	0.352
250.00	0.621
125.00	0.857
62.50	1.156
31.25	1.565
15.63	1.775
0.00	2.123

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 PGI2 and the recovery rates were calculated by comparing the measured value to the expected amount of PGI2 in samples.

Matrix	Recovery range	Average
serum(n=5)	82-97%	89%
EDTA plasma(n=5)	95-108%	101%
Heparin plasma(n=5)	80-95%	86%

線性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of PGI2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.