人过氧化脂质(LPO)微量上样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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人过氧化脂质(LPO)微量上样酶联免疫吸附检测试剂盒

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ELK9572MS

规格：	价格：
48T	￥1960.00
96T	￥2800.00
96T*5	￥11900.00

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Overview

Product name:	Human LPO(Lipid Peroxide) Microsample ELISA Kit
Reactivity:	Human
Alternative Names:	Lipid Peroxide; LPO
Assay Type:	Sandwich
Sensitivity:	0.056 ng/mL
Standard:	10 ng/mL
Detection Range:	0.16-10 ng/mL
Sample Type:	serum, plasma and other biological fluids
Assay Length:	3.5h
Research Area:	Enzyme & Kinase;Infection immunity;
Test principle:	The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human LPO. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LPO. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human LPO, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 LPO in the samples is then determined by comparing the OD of the samples to the standard curve.

标准曲线

Concentration (ng/mL)	OD	Corrected OD
10.00	2.033	1.942
5.00	1.596	1.505
2.50	1.245	1.154
1.25	0.756	0.665
0.63	0.598	0.507
0.31	0.333	0.242
0.16	0.206	0.115
0.00	0.091	0.000

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

Matrix	Recovery range	Average
serum(n=5)	94-103%	99%
EDTA plasma(n=5)	92-101%	97%
Heparin plasma(n=5)	86-106%	96%

线性

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