MDA (Malondialdehyde) ELISA Kit
This assay employs the competitive inhibition enzyme immunoassay technique. The micro-plate provided in this kit has been pre-coated with Malondialdehyde (MDA) protein. Standards or samples are then added to the appropriate micro-plate wells with a biotin-conjugated antibody specific to Malondialdehyde (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 Malondialdehyde (MDA) in the samples is then determined by comparing the OD of the samples to the standard curve.
Kit Components:
1) Pre-coated Microplate [12 strips x 8 wells]
2) 100x Biotinylated Conjugate [120ul]
3) Biotinylated Conjugate Diluent [10ml]
4) 100x Streptavidin-HRP [120ul]
5) HRP Diluent [12ml]
6) TMB Substrate Solution [9ml]
7) 25x Wash Buffer [20ml]
8) Stop reagent [6ml]
9) Lyophilized Standard [2]
10) Standard Diluent Buffer [20ml]
11) Plate Sealers [2]
12) User Maual [1]
Size |
1 x 96 Well Plate |
Product Category |
ELISA (RUO) |
Reactivity |
General |
Sample Source |
Serum; Plasma; Other Biological Fluids |
Assay Method |
Competitive Inhibition ELISA |
Detection Range |
31.25-2000ng/mL |
Sensitivity |
9.15ng/mL |
Assay Duration |
2h |
Storage/Stability |
-20°C/1 year; 4°C/6 months |
Shipping |
Gel Packs |