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Home >> Antibodies >> p504S Antibody / Prostate Cancer Marker Antibody

p504S Antibody / Prostate Cancer Marker Antibody [clone 13H4] (V8770)

  Catalog No Formulation Size Price (USD)  
Image V8770-100UG 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide 100 ug 559
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V8770-20UG 0.2 mg/ml in 1X PBS with 0.1 mg/ml BSA (US sourced) and 0.05% sodium azide 20 ug 259
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V8770SAF-100UG 1 mg/ml in 1X PBS; BSA free, sodium azide free 100 ug 559
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p504S Antibody Prostate Carcinoma IHC. Immunohistochemistry staining of formalin-fixed, paraffin-embedded human prostate carcinoma tissue using clone 13H4 demonstrates strong granular cytoplasmic red chromogenic staining in malignant prostatic epithelial cells, consistent with the characteristic expression pattern of Alpha-methylacyl-CoA racemase / AMACR in prostate adenocarcinoma. The staining highlights neoplastic glandular architecture with comparatively minimal background signal in surrounding stromal tissue.
p504S Antibody Prostate Carcinoma IHC. Immunohistochemistry staining of formalin-fixed, paraffin-embedded human prostate carcinoma tissue using clone 13H4 demonstrates granular cytoplasmic red chromogenic staining within malignant prostatic epithelial cells, consistent with the established expression pattern of Alpha-methylacyl-CoA racemase / AMACR in prostate adenocarcinoma. Variable staining intensity among neoplastic glands highlights the heterogeneous expression profile commonly observed for carcinoma-associated metabolic markers in prostate tumor tissue.
p504S Antibody Prostate Carcinoma IHC. Immunohistochemistry staining of FFPE human prostate carcinoma tissue using clone 13H4 demonstrates strong granular cytoplasmic HRP-DAB brown staining in malignant prostatic epithelial cells, consistent with the characteristic expression pattern of Alpha-methylacyl-CoA racemase / AMACR in prostate adenocarcinoma. The staining prominently highlights neoplastic glandular architecture with comparatively limited background signal in surrounding stromal tissue. HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing.
p504S Antibody Renal Cell Carcinoma IHC. Immunohistochemistry staining of FFPE human renal cell carcinoma tissue using clone 13H4 demonstrates strong granular cytoplasmic HRP-DAB brown staining in malignant epithelial cells, consistent with carcinoma-associated expression of Alpha-methylacyl-CoA racemase / AMACR in renal malignancy tissue. The staining pattern highlights tumor glandular and tubular structures with comparatively limited background signal in surrounding stromal elements. HIER: boil tissue sections in pH 9 10mM Tris with 1mM EDTA for 20 min and allow to cool before testing.
p504S Antibody Human Kidney WB. Western blot analysis of human kidney lysate using clone 13H4 demonstrates a distinct band at approximately 40-43 kDa, consistent with the predicted molecular weight of Alpha-methylacyl-CoA racemase / AMACR. The observed signal supports expression of this carcinoma-associated metabolic enzyme in renal tissue and aligns with the established molecular profile of p504S.
p504S Antibody Kidney Tissue WB. Western blot analysis of human, mouse, rat, hamster, and guinea pig kidney tissue lysates using p504S Antibody clone 13H4 demonstrates a major band at approximately 40-42 kDa in human, mouse, rat, and guinea pig samples, consistent with the predicted molecular weight of Alpha-methylacyl-CoA racemase / AMACR. Variable signal intensity across species may reflect differential epitope conservation or tissue expression levels of this peroxisomal and mitochondrial metabolic enzyme involved in branched-chain fatty acid and bile acid metabolism.
p504S Antibody Protein Array Specificity Analysis. Analysis of protein microarray containing more than 19,000 full-length human proteins using p504S Antibody clone 13H4 identified AMACR as the top-ranked target with a Z-score of 60.59 and an S-score of 37.19, supporting highly specific recognition of Alpha-methylacyl-CoA racemase / AMACR. The Z-score represents the signal intensity generated by antibody binding relative to the mean signal across the array, while the S-score reflects the difference in signal strength between successive ranked targets. Because an S-score greater than 2.5 is considered supportive of target specificity, the markedly elevated S-score observed for clone 13H4 demonstrates strong preferential binding to AMACR relative to other proteins present on the array.
Availability 1-3 business days
Species Reactivity Human, Mouse, Guinea pig
Format Purified
Host Rabbit
Clonality Rabbit Monoclonal
Isotype Rabbit IgG
Clone Name 13H4
Purity Protein A affinity chromatography
UniProt Q9UHK6
Localization Cytoplasmic
Applications Immunohistochemistry (FFPE) : 1-2ug/ml (Human)
Western Blot : 1-2ug/ml (Human/Mouse/Guinea pig)
Limitations This p504S Antibody / Prostate Cancer Marker Antibody is available for research use only.
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Description

Alpha-methylacyl-CoA racemase (AMACR) is a peroxisomal and mitochondrial metabolic enzyme involved in branched-chain fatty acid metabolism and bile acid biosynthesis. p504S Antibody / Prostate Cancer Marker Antibody recognizes AMACR, a widely studied carcinoma-associated metabolic enzyme that is frequently overexpressed in prostate adenocarcinoma and additional epithelial malignancies.

p504S antibody, also referred to as AMACR antibody and Alpha-methylacyl-CoA racemase antibody in the literature, is extensively used in prostate cancer research and diagnostic pathology applications. Clone 13H4 antibody has been cited in numerous peer-reviewed publications and is broadly recognized as a historically important p504S monoclonal antibody for investigating prostate carcinoma-associated metabolic reprogramming and epithelial tumor biology.

AMACR expression is commonly elevated in prostate adenocarcinoma relative to benign prostatic glands, contributing to the widespread use of p504S antibodies in studies examining prostate tumor differentiation and carcinoma-associated biomarker expression. In immunohistochemistry applications, AMACR typically demonstrates granular cytoplasmic staining within malignant epithelial cells, reflecting its localization to intracellular metabolic organelles including peroxisomes and mitochondria.

Beyond prostate cancer, increased AMACR expression has also been reported in colorectal carcinoma, hepatocellular carcinoma, renal tumors, and additional epithelial malignancies. The enzyme participates in lipid metabolic pathways associated with branched-chain fatty acid degradation, supporting growing interest in AMACR as a marker of tumor-associated metabolic adaptation and altered fatty acid utilization.

Western blot analysis using clone 13H4 commonly identifies AMACR near 40-42 kDa, consistent with the predicted molecular weight of the mature protein. Protein microarray analysis containing more than 19,000 full-length human proteins identified AMACR as the dominant target recognized by clone 13H4, supporting strong preferential binding to Alpha-methylacyl-CoA racemase relative to unrelated proteins on the array.

The longstanding use of p504S antibodies in cancer pathology research has contributed to the broad recognition of AMACR as a clinically relevant prostate carcinoma marker and metabolism-associated tumor biomarker. Continued interest in cancer metabolism, lipid utilization pathways, and epithelial differentiation biology further supports the utility of p504S antibodies in modern tumor biology research applications.

Together, the available western blot, immunohistochemistry, publication history, and protein array specificity data support the use of clone 13H4 for investigating AMACR expression and carcinoma-associated metabolic signaling pathways in epithelial tumor biology.

For additional AMACR and p504S research antibodies validated by protein microarray specificity analysis, western blotting, and immunohistochemistry, explore the broader AMACR Antibody page featuring clone AMACR/1864.

Application Notes

Optimal dilution of the p504S Antibody / Prostate Cancer Marker 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.

Immunogen

Full length human recombinant protein was used as the immunogen for the p504S antibody.

Storage

Store the p504S antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).

Alternate Names

p504S antibody, AMACR antibody, Alpha-methylacyl-CoA racemase antibody, prostate carcinoma marker antibody, clone 13H4 antibody

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