- Quantitative determination of HNE-histidine in human cell lysates - Indirect enzyme immunoassay- Based on a well described monoclonal antibody used in ICC, IHC & WB- Range of detection between 71pmol/mg and 857pmol/mg- Human plasma spiking tested- Tissue homogenates have not been tested yet
(E)-4-Hydroxynonenal (HNE) is one of the most important breakdown products and reliable marker of lipid peroxidation (LPO). This indirect enzyme immunoassay (EIA) allows for the first time the quantitative determination of HNE-histidine conjugates from lysates of human cells which were exposed to strong oxidative stress.
Prepare 500-5'000-fold dilution (~10-1µM) in phosphate buffer (0.1M phosphate, pH 7.4) immediately before use. BSA, phenol red and amines may affect the fluorescence and must be used with caution. Do not store the dilutions.