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Human IFNa21(Interferon Alpha 21) ELISA Kit
ELK3492
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48 T $320.00
96 T $458.00
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Overview

Product name: Human IFNa21(Interferon Alpha 21) ELISA Kit
Reactivity: Human
Alternative Names: LeIF F; Interferon alpha-F
Assay Type: Sandwich
Sensitivity: 6.2 pg/mL
Standard: 1000 pg/mL
Detection Range: 15.63-1000 pg/mL
Sample Type: Serum, plasma and other biological fluids.
Assay Length: 3.5h
Research Area: Cytokine;
Uniprot ID: P01568
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 Human IFNa21. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human IFNa21. 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 Human IFNa21, 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 Human IFNa21 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 2.121 2.039
500.00 1.647 1.565
250.00 1.235 1.153
125.00 0.872 0.790
62.50 0.556 0.474
31.25 0.335 0.253
15.63 0.216 0.134
0.00 0.082 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 IFNa21 and the recovery rates were calculated by comparing the measured value to the expected amount of IFNa21 in samples.
Matrix Recovery range Average
serum(n=5) 95-107% 101%
EDTA plasma(n=5) 96-104% 100%
Heparin plasma(n=5) 98-104% 102%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of IFNa21 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) 95-106% 83-96% 87-98% 78-89%
EDTA plasma(n=5) 83-101% 90-99% 87-103% 89-97%
Heparin plasma(n=5) 85-94% 95-103% 79-97% 93-102%