| Code | CSB-RA145644A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| IF | 1:50-1:200 |
| FC | 1:50-1:200 |
Alcohol dehydrogenase 4 (ADH4) belongs to the class II alcohol dehydrogenase family and plays a central role in ethanol metabolism, catalyzing the oxidation of alcohols to aldehydes in the liver. Beyond its well-characterized function in alcohol processing, ADH4 also exhibits aldehyde reductase activity, positioning it as a relevant target for researchers investigating hepatic metabolism, toxicology, and signal transduction pathways. Understanding ADH4 expression and localization provides valuable insights into metabolic disorders, liver function, and individual variations in alcohol metabolism.
This recombinant monoclonal antibody, clone 7A5, offers the reproducibility and consistency that demanding experimental workflows require. Developed using recombinant technology with a defined sequence, this rabbit IgG eliminates the lot-to-lot variability that can compromise longitudinal studies or multi-site collaborations. The antibody was raised against a synthetic peptide derived from human ADH4 and has been validated for human sample reactivity, making it particularly suited for clinical and translational research applications.
Validation studies demonstrate reliable performance across multiple detection platforms. Immunofluorescence analysis of HepG2 cells, a human hepatocellular carcinoma line with preserved hepatic characteristics, reveals clear cytoplasmic staining at dilutions of 1:50 to 1:200. Flow cytometry experiments using the same cell line confirm specific detection, with distinct positive population shifts compared to isotype controls when used at 1:50 to 1:200 dilutions. The antibody is additionally compatible with ELISA applications, providing flexibility for quantitative expression studies.
Supplied in a stabilized liquid format with glycerol for convenient long-term storage, this affinity-purified antibody supports researchers exploring hepatic metabolism, alcohol-related pathologies, and broader signal transduction mechanisms involving ADH4.
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