GuineaPig dystrophin ELISA Kit | Dystrophin elisa kit
Guinea Pig dystrophin ELISA Kit
Reactivity
GuineaPig
Synonyms
dystrophin; Guinea Pig dystrophin ELISA Kit; Guinea Pig dystrophin (Dystrophin) ELISA Kit; Guinea Pig Pig dystrophin ELISA Kit; dystrophin (Guinea Pig Pig); Dystrophin elisa kit
Reactivity
GuineaPig
Assay Type
Sandwich
Preparation and Storage
Store all reagents at 2-8 degree C
Typical Testing Data/Standard Curve (for reference only)
Related Product Information for Dystrophin elisa kit
Intended Uses: This DYSTROPHIN ELISA kit is intended Laboratory for research use only.The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration ofDYSTROPHIN in the sample, thisDYSTROPHIN ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versusDYSTROPHIN concentration. The concentration ofDYSTROPHIN in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Principle of the Assay: This DYSTROPHIN enzyme linked immunosorbent assay applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific forDYSTROPHIN. Standards or samples are then added to the microtiter plate wells andDYSTROPHIN if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount ofDYSTROPHIN present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific forDYSTROPHIN are added to each well to "sandwich" theDYSTROPHIN immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, A and B substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period.Only those wells that containDYSTROPHIN and enzyme-conjugated antibody will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the colour change is measured spectrophotometrically at a wavelength of 450 nm.
Principle of the Assay: This DYSTROPHIN enzyme linked immunosorbent assay applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific forDYSTROPHIN. Standards or samples are then added to the microtiter plate wells andDYSTROPHIN if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount ofDYSTROPHIN present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific forDYSTROPHIN are added to each well to "sandwich" theDYSTROPHIN immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, A and B substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period.Only those wells that containDYSTROPHIN and enzyme-conjugated antibody will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the colour change is measured spectrophotometrically at a wavelength of 450 nm.
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