Human AP36(Apelin 36) ELISA Kit – ATO2243
ATO2243
Size:Price:
48 T$320.00
96 T$458.00
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Overview

Product name: Human AP36(Apelin 36) ELISA Kit
Reactivity: Human
Alternative Names: APLN36
Assay Type: Competitive Inhibition
Sensitivity: 2.52 pg/mL
Standard: 600 pg/mL
Detection Range: 9.38-600 pg/mL
Sample Type: Serum, plasma and other biological fluids
Assay Length: 2h
Research Area: Metabolic pathway;Endocrinology;Gastroenterology;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human AP36 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human AP36. 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 AP36 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
600.00 0.212
300.00 0.357
150.00 0.611
75.00 0.833
37.50 1.156
18.75 1.511
9.38 1.775
0.00 2.123

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 AP36 and the recovery rates were calculated by comparing the measured value to the expected amount of AP36 in samples.
Matrix Recovery range Average
serum(n=5) 85-97% 91%
EDTA plasma(n=5) 83-99% 95%
Heparin plasma(n=5) 85-97% 91%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of AP36 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) 79-91% 87-96% 92-101% 82-95%
EDTA plasma(n=5) 95-102% 83-96% 97-105% 85-97%
Heparin plasma(n=5) 93-105% 85-97% 90-99% 82-101%