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Human NMU(Neuromedin U) ELISA Kit
ELK5062
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48 T $320.00
96 T $458.00
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Overview

Product name: Human NMU(Neuromedin U) ELISA Kit
Reactivity: Human
Alternative Names: NM-U
Assay Type: Competitive Inhibition
Sensitivity: 48.3 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: Endocrinology;Cardiovascular biology;Neuro science;Gastroenterology;Hormone metabolism;Bone metabolism;
Uniprot ID: P48645
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human NMU protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NMU. 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 NMU 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
10000.00 0.189
5000.00 0.397
2500.00 0.583
1250.00 0.833
625.00 1.157
312.50 1.583
156.25 1.715
0.00 2.211

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 NMU and the recovery rates were calculated by comparing the measured value to the expected amount of NMU in samples.
Matrix Recovery range Average
serum(n=5) 88-102% 95%
EDTA plasma(n=5) 83-96% 89%
Heparin plasma(n=5) 92-107% 101%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of NMU 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) 85-107% 84-98% 89-97% 85-94%
EDTA plasma(n=5) 91-99% 83-89% 88-104% 97-103%
Heparin plasma(n=5) 85-96% 85-96% 93-99% 87-101%