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Product name: Human NPY(Neuropeptide Y) ELISA Kit
Catalogue No: ELK2447
Alternative Names: NP-Y; PYY4; CPON; Pro-neuropeptide Y; Neuropeptide tyrosine; C-flanking peptide of NPY
Assay Type: Sandwich
Sensitivity: 9.18 pg/mL
Standard: 2000 pg/mL
Range: 31.25-2000 pg/mL

Description

Product name: Human NPY(Neuropeptide Y) ELISA Kit
Reactivity: Human
Alternative Names: NP-Y; PYY4; CPON; Pro-neuropeptide Y; Neuropeptide tyrosine; C-flanking peptide of NPY
Assay Type: Sandwich
Sensitivity: 9.18 pg/mL
Standard: 2000 pg/mL
Range: 31.25-2000 pg/mL
Sample Type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Length: 3.5h
Research Area: Metabolic pathway;Endocrinology;Cardiovascular biology;Neuro science;Hepatology;
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 Neuropeptide Y(NPY). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Neuropeptide Y(NPY). 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 Neuropeptide Y(NPY), 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 Neuropeptide Y(NPY) in the samples is then determined by comparing the OD of the samples to the standard curve.
Standard Curve

Concentration (ng/mL) OD Corrected OD
2000.00 2.156 2.058
1000.00 1.586 1.488
500.00 1.283 1.185
250.00 0.815 0.717
125.00 0.541 0.443
62.50 0.262 0.164
31.25 0.238 0.140
0.00 0.098 0.000
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 NPY and the recovery rates were calculated by comparing the measured value to the expected amount of NPY in samples.
Matrix Recovery range Average
serum(n=5) 80-95% 87%
EDTA plasma(n=5) 83-95% 89%
Heparin plasma(n=5) 80-97% 88%
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of NPY 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) 87-94% 85-96% 89-100% 85-96%
EDTA plasma(n=5) 85-94% 87-101% 86-97% 88-95%
Heparin plasma(n=5) 92-101% 87-98% 85-92% 79-96%
Note For Research Use Only

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