Human AP13(Apelin 13) ELISA Kit – ATO2252
ATO2252
Size:Price:
48 T$320.00
96 T$458.00
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Overview

Product name: Human AP13(Apelin 13) ELISA Kit
Reactivity: Human
Alternative Names: APLN13
Assay Type: Competitive Inhibition
Sensitivity: 8.24 pg/mL
Standard: 1600 pg/mL
Detection Range: 25-1600 pg/mL
Sample Type: Serum, plasma and other biological fluids
Assay Length: 2h
Research Area: Metabolic pathway;Endocrinology;Cardiovascular biology;Neuro science;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 AP13 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human AP13. 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 AP13 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
1600.00 0.227
800.00 0.386
400.00 0.583
200.00 0.857
100.00 1.152
50.00 1.511
25.00 1.789
0.00 2.115

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 AP13 and the recovery rates were calculated by comparing the measured value to the expected amount of AP13 in samples.
Matrix Recovery range Average
serum(n=5) 77-95% 86%
EDTA plasma(n=5) 92-106% 99%
Heparin plasma(n=5) 88-103% 95%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of AP13 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) 85-94% 87-96% 95-103% 85-91%
EDTA plasma(n=5) 85-92% 90-96% 95-102% 87-98%
Heparin plasma(n=5) 93-102% 90-99% 95-106% 87-101%