- Tel: 858.663.9055
-
Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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p504S antibody detects alpha-methylacyl-CoA racemase, an enzyme encoded by the AMACR gene. p504S is strongly expressed in prostate carcinoma and is considered one of the most reliable markers for prostate cancer pathology. Because p504S is absent or weak in benign prostate tissue but upregulated in malignancy, p504S antibody is indispensable in oncology, diagnostic pathology, and urology.
AMACR functions in the beta-oxidation of branched-chain fatty acids and bile acid intermediates. Its enzymatic activity contributes to lipid metabolism in peroxisomes and mitochondria. Dysregulated AMACR expression has been linked not only to prostate cancer but also to other malignancies, including colorectal carcinoma and renal cell carcinoma. p504S serves as a robust marker of prostatic malignancy in pathology practice.
The p504S antibody clone 13H4 provides specific and reproducible recognition. Clone 13H4 has been cited extensively in peer-reviewed publications investigating prostate cancer diagnosis, biomarker validation, and cancer metabolism. Its reproducibility makes it suitable for immunohistochemistry, immunoblotting, and tissue-based diagnostics where accuracy is critical.
Research using clone 13H4 has confirmed that p504S expression distinguishes malignant from benign prostatic glands, even in challenging or borderline cases. In oncology, detection of AMACR complements PSA and basal cell markers in diagnostic panels. This antibody has also supported studies investigating metabolic reprogramming in cancer, where AMACR overexpression contributes to altered lipid metabolism and tumor growth.
NSJ Bioreagents provides this p504S antibody to support oncology, urology, and cancer metabolism research. Alternate names include AMACR antibody, alpha-methylacyl-CoA racemase antibody, prostate cancer marker antibody, fatty acid metabolism enzyme antibody, and metabolic biomarker antibody.
Optimal dilution of the p504S antibody should be determined by the researcher.
1. Staining of formalin-fixed tissues requires boiling tissue sections in 10mM Tris with 1mM EDTA, pH 9.0, for 10-20 min followed by cooling at RT for 20 min
2. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.
Full length human recombinant protein was used as the immunogen for the p504S antibody.
Store the p504S antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
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