IFN-gamma (Human) ELISA Kit

Kits

貨號 Cat. No.
E4825-100
規格 Size
E4825-100
Reactivity
Human
Sample Type
Other biological fluids 、 Plasma 、 Serum

Description




Alternate Name : IFNG, IFG, IFI, Type II Interferon


 

Tag Line :


A Sandwich ELISA kit for the quantitative measurement of human IFN-γ in plasma, tissue homogenates and other biological fluids.


 

Storage Conditions: 4ºC


 

Shelf life: 12 months


 

Summary :



 

Detection Method: Sandwich ELISA, Absorbance (450 nm)


 

Features & Benefits:


Specificity: No Significant cross-reactivity or interference between Human IFN-γ and analogues was observed.,Detection Range: 15.63-1000 pg/mL,Precision: Coefficient of variation is < 10%.,Sensitivity: 9.38 pg/mL


 

Description:


IFN-gamma is produced by lymphocytes activated by specific antigens or mitogens. IFN-gamma, in addition to having antiviral activity, has important immunoregulatory functions. It is a potent activator of macrophages, it has antiproliferative effects on transformed cells and it can potentiate the antiviral and antitumor effects of the type I interferons. BioVision’s IFN-gamma (Human) ELISA kit is based on Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human IFN-gamma. Standards or samples are added to the micro ELISA plate wells that bind to the specific antibody. Then a biotinylated detection antibody specific for Human IFN-gamma and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. The wells are washed, a TMB substrate solution is added to the wells and blue color develops in proportion to the amount of IFN-gamma bound. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The OD value is proportional to the concentration of Human IFN-gamma. The concentration of Human IFN-gamma in the samples can be calculated by comparing the OD of the samples to the standard curve.


 





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