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人神经介素B(NMB)酶联免疫吸附检测试剂盒

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ELK1629

规格：	价格：
48T	￥1960.00
96T	￥2800.00

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Overview

Product name:	Human NMB(Neuromedin B) ELISA Kit
Reactivity:	Human
Alternative Names:	NM-B
Assay Type:	Competitive Inhibition
Sensitivity:	48.1 pg/mL
Standard:	10000 pg/mL
Detection Range:	156.25-10000 pg/mL
Sample type:	serum, plasma and other biological fluids
Assay length:	2h
Research Area:	Signal transduction;Endocrinology;Neuro science;Gastroenterology;Hormone metabolism;
Uniprot ID:	P08949
Test principle:	This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human NMB. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NMB. 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 Human NMB 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
10000.00	0.237
5000.00	0.411
2500.00	0.692
1250.00	0.933
625.00	1.253
312.50	1.587
156.25	1.861
0.00	2.375

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

Matrix	Recovery range	Average
serum(n=5)	77-95%	86%
EDTA plasma(n=5)	94-106%	100%
Heparin plasma(n=5)	80-97%	88%

线性

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