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Zebrafish MDA (Malondialdehyde) ELISA Kit

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Zebrafish MDA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Zebrafish MDA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Zebrafish MDA in the samples is then determined by comparing the OD of the samples to the standard curve.

Product Specifications

Product Name Alternative

Malondialdehyde; MDA

Reactivity

Zebrafish

Field of Research

Metabolic pathway; Hepatology; Hormone metabolism

Assay Type

Competitive Inhibition

Assay Principle

This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Zebrafish MDA. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Zebrafish MDA. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. 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 Zebrafish MDA in the samples is then determined by comparing the OD of the samples to the standard curve.

Assay Performance Time

2h

Standard

2000 ng/mL

Sample Type

Serum, plasma and other biological fluids

Detection Range

31.25-2000 ng/mL

Sensitivity

9.15 ng/mL

Available Sizes

Frequently Asked Questions

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