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SpecificityThis assay has high sensitivity and excellent specificity for detection of Human BAD. No significant cross-reactivity or interference between Human BAD and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human BAD and all the analogues, therefore, cross reaction may still exist.
Intended UseHuman BAD ELISA Kit allows for the in vitro quantitative determination of BAD , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
StorageStore the whole ELISA kit at 4℃
Product Description specificalDescription: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of BAD in human serum, plasma and other biological fluids
Principle of the Assay: This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human BAD. Standards or samples are added to the appropriate micro ELISA plate wells and bound by the specific antibody. Then a biotinylated detection antibody specific for Human BAD and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human BAD, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of Human BAD. You can calculate the concentration of Human BAD in the samples by comparing the OD of the samples to the standard curve.
Human Bcl2-associated agonist of cell death Protein information
Q92934; O14803; Q6FH21;
Human Bcl2-associated agonist of cell death Protein SEQUENCE