Monoclonal Antibody to AMACR / p504S (Prostate Cancer Marker)(Clone : 13H4), Clone: [13H4], Rabbit

Artikelnummer: ABI-36-1144
Artikelname: Monoclonal Antibody to AMACR / p504S (Prostate Cancer Marker)(Clone : 13H4), Clone: [13H4], Rabbit
Artikelnummer: ABI-36-1144
Hersteller Artikelnummer: 36-1144
Alternativnummer: ABI-36-1144-100UG
Hersteller: Abeomics
Wirt: Rabbit
Kategorie: Antikörper
Applikation: IHC, WB
Spezies Reaktivität: Human
Immunogen: Full length human recombinant AMACR protein
Alternative Synonym: AMACR
This antibody recognizes a protein of 54kDa, which is identified as AMACR, also known as p504S. It is an enzyme that is involved in bile acid biosynthesis and beta-oxidation of branched-chain fatty acids. AMACR is essential in lipid metabolism. It is expressed in cells of premalignant high-grade prostatic intraepithelial neoplasia (HGPIN) and prostate adenocarcinoma. The majority of the carcinoma cells show a distinct granular cytoplasmic staining reaction. AMACR is present at low or undetectable levels in glandular epithelial cells of normal prostate and benign prostatic hyperplasia. A spotty granular cytoplasmic staining is seen in a few cells of the benign glands. AMACR is expressed in normal liver (hepatocytes), kidney (tubular epithelial cells) and gall bladder (epithelial cells). Expression has also been found in lung (bronchial epithelial cells) and colon (colonic surface epithelium). AMACR expression can also be found in hepatocellular carcinoma and kidney carcinoma. Past studies have also shown that AMACR is expressed in various colon carcinomas (well, moderately and poorly differentiated) and over expressed in prostate carcinoma.
Klonalität: Monoclonal
Klon-Bezeichnung: [13H4]
NCBI: 23600
UniProt: Q9UHK6
Reinheit: Affinity Chromatography
Formulierung: Purified
Target-Kategorie: AMACR / p504S (Prostate Cancer Marker)
Application Verdünnung: Western Blot (1:50-1:100), Immunohistochemistry (Formalin-fixed) (1:50-1:100 for 30-60 minutes at RT)(Staining of formalin-fixed tissues requires heating tissue sections in 1mM EDTA, pH 7.5-8.5, for 45 min at 95&degC followed by cooling at RT for 20 m