人神經肽S(NPS)酶聯免疫吸附檢測試劑盒-武汉义森科技有限责任公司

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人神經肽S(NPS)酶聯免疫吸附檢測試劑盒

ELK1061

規格：	價格：
48T	￥1680.00
96T	￥2400.00

下(xià)載說明 ①

Overview

Product name:	Human NPS(Neuropeptide S) ELISA Kit
Reactivity:	Human
Alternative Names:	NP-S
Assay Type:	Competitive Inhibition
Sensitivity:	4.48 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:	Neuro science;Hormone metabolism;
Uniprot ID:	P0C0P6
Test principle:	This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human NPS protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NPS. 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 NPS in the samples is then determined by comparing the OD of the samples to the standard curve.

标準曲線

Concentration (pg/mL)	OD	Corrected OD
1000.00	0.108
500.00	0.214
250.00	0.318
125.00	0.527
62.50	0.824
31.25	1.109
15.63	1.724
0.00	2.167

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

Matrix	Recovery range	Average
serum(n=5)	96-104%	100%
EDTA plasma(n=5)	98-104%	102%
Heparin plasma(n=5)	95-107%	101%

線性

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