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白三烯B4(LTB4)酶联免疫吸附检测试剂盒

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ELK7887

规格：	价格：
48T	￥1680.00
96T	￥2400.00

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Overview

Product name:	LTB4(Leukotriene B4) ELISA Kit
Reactivity:	General
Alternative Names:	LT-B4
Assay Type:	Competitive Inhibition
Sensitivity:	91.1 pg/mL
Standard:	20000 pg/mL
Detection Range:	312.5-20000 pg/mL
Sample type:	serum, plasma, tissue homogenates, cell culture supernates 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 LTB4. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to LTB4. 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 LTB4 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
20000.00	0.191
10000.00	0.352
5000.00	0.577
2500.00	0.833
1250.00	1.197
625.00	1.578
312.50	1.789
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 LTB4 and the recovery rates were calculated by comparing the measured value to the expected amount of LTB4 in samples.

Matrix	Recovery range	Average
serum(n=5)	80-96%	88%
EDTA plasma(n=5)	80-92%	86%
Heparin plasma(n=5)	78-95%	87%

线性

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of LTB4 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.