catalog number :
MBS733783
products type :
ELISA Kit
products full name :
Rat Estrogens ELISA Kit
products short name :
Estrogens
products name syn :
Rat Estrogens (ES) ELISA Kit; Rat Estrogens ELISA Kit; Estrogens; Estrogens ELISA Kit (Rat)
specificity :
This assay has high sensitivity and excellent specificity for detection of ES. No significant cross-reactivity or interference between ES and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ES and all the analogues, therefore, cross reaction may still exist in some cases.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate. Assay Type: Sandwich. Sensitivity: 0.1 ng/mL.
other info2 :
Intended Uses: This ES ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat ES. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
products categories :
Rat ELISA Kit
products description :
Principle of the assay: ES ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for ES. Standards or samples are then added to the microtiter plate wells and ES if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of ES present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for ES are added to each well to "sandwich" the ES immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain ES and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ES concentration in each sample is interpolated from this standard curve.