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產(chǎn)品中心

晚期糖基化終末產(chǎn)物(AGE)酶聯(lián)免疫吸附檢測(cè)試劑盒

ELK1890

規(guī)格：	價(jià)格：
48T	￥1960.00
96T	￥2800.00

下載說(shuō)明 ①

Overview

Product name:	AGE(Advanced Glycation End Product) ELISA Kit
Reactivity:	General
Alternative Names:	AGEs; Advanced Glycation End Products
Assay Type:	Competitive Inhibition
Sensitivity:	38.2 ng/mL
Standard:	8000 ng/mL
Detection Range:	125-8000 ng/mL
Sample Type:	serum, plasma and other biological fluids
Assay Length:	2h
Research Area:	Metabolic pathway;Endocrinology;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 AGE protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to AGE. 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 AGE in the samples is then determined by comparing the OD of the samples to the standard curve.

標(biāo)準(zhǔn)曲線

Concentration (ng/mL)	OD	Corrected OD
8000.00	0.191
4000.00	0.396
2000.00	0.583
1000.00	0.857
500.00	1.156
250.00	1.511
125.00	1.762
0.00	2.132

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

Matrix	Recovery range	Average
serum(n=5)	85-97%	91%
EDTA plasma(n=5)	83-95%	89%
Heparin plasma(n=5)	80-92%	86%

線性

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