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Human NPS(Neuropeptide S) ELISA Kit
ELK1061
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48 T $265.00
96 T $376.00
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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.

Standard curve

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

Precision

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.

Recovery

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%

Linearity

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.
Matrix 1:2 1:4 1:8 1:16
serum(n=5) 82-94% 95-102% 87-103% 88-95%
EDTA plasma(n=5) 87-95% 78-91% 97-103% 95-101%
Heparin plasma(n=5) 85-94% 87-99% 85-101% 79-90%