Lablisa® FastTrack Human IFNg(Interferon Gamma) ELISA Kit

Product Information

Lablisa® FastTrack Human IFNg(Interferon Gamma) ELISA Kit

Catalog No : LAB067FT | Pack Size : 48T , 96T

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 IFN-γ, and the Human IFN-γ standard plate wells that pre-coated using protein-related techniques are provided separately. Standard/Sample Diluent Buffer or samples are added to the appropriate microtiter plate wells ,then added a HRP-conjugated antibody specific to Human IFN-γ. After TMB substrate solution is added, only those wells that contain Human IFN-γ and HRP-conjugated antibody 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 IFN-γ in the samples is then determined by comparing the OD of the samples to the standard curve.

Product name:Lablisa® FastTrack Human IFNg(Interferon Gamma) ELISA Kit
Reactivity:Human
Alternative Names:IFN gamma; IFN-G; IFG; IFI; INFr; IFN; Immune Interferon
Assay Type:Sandwich
Sensitivity:15 pg/mL
Standard:1000 pg/mL
Detection Range:15.63-1000 pg/mL
Sample Type:Serum, plasma, cell
Assay Length:1.5h
Research Area:Cytokine;Infection immunity;

Standard curve



Concentration (pg/mL)ODCorrected OD
1000.002.0381.930
500.001.5211.413
250.001.1861.078
125.000.8920.784
62.500.4470.339
31.250.4810.373
15.630.2260.118
0.000.1080.000


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 IFN-γ and the recovery rates were calculated by comparing the measured value to the expected amount of IFN-γ in samples.

MatrixRecovery rangeAverage
serum(n=5)82-95%88%
EDTA plasma(n=5)80-95%87%
Heparin plasma(n=5)86-99%92%


Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of IFN-γ and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Matrix1:21:41:81:16
serum(n=5)95-103%79-96%93-106%87-98%
EDTA plasma(n=5)86-93%93-101%85-98%90-101%
Heparin plasma(n=5)78-92%79-93%94-106%83-97%


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