- Tel: 858.663.9055
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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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Opa-interacting protein 4 (OIP-4), also known as Preferentially expressed antigen in melanoma (PRAME), is a cancer-testis antigen involved in transcriptional regulation, cellular differentiation control, and tumor-associated immune signaling pathways. OIP-4 Antibody / Cancer-Testis Antigen is useful for studying malignancy-associated antigen expression, tumor immunology, and cancer-associated transcriptional regulation mechanisms. OIP-4 antibody, also referred to as PRAME antibody and Preferentially expressed antigen in melanoma antibody in the literature, recognizes a tumor-associated antigen broadly expressed across multiple malignancies while demonstrating restricted expression in most normal tissues.
PRAME is predominantly localized within the nucleus where it participates in transcription-associated signaling pathways regulating cellular proliferation, retinoic acid responsiveness, and differentiation programs. Expression of OIP-4 is generally limited in normal tissues but becomes elevated in melanoma, leukemia, sarcoma, ovarian carcinoma, breast carcinoma, lung cancer, and additional malignancies associated with tumor progression and immune recognition pathways. Because of this restricted normal tissue distribution and broad tumor-associated expression profile, PRAME has become highly relevant in cancer immunology and diagnostic pathology research.
OIP-4-associated signaling pathways have been investigated in tumor immune evasion, oncogenic transcriptional reprogramming, and antigen-directed therapeutic strategies. PRAME expression has also become important in studies examining melanoma classification, metastatic progression, and immunotherapy development. In pathology research, PRAME immunohistochemistry is commonly used to evaluate melanocytic lesions and assist in distinguishing malignant melanoma from benign melanocytic proliferations. Expression patterns have additionally been studied in hematologic malignancies and soft tissue tumors associated with aberrant transcriptional regulation pathways.
Because OIP-4 functions as a tumor-associated nuclear antigen linked to cancer-testis biology, this target remains highly relevant for studies focused on tumor classification, cancer-associated immune signaling, and transcriptional regulation within malignant cells. Immunohistochemistry studies commonly demonstrate nuclear staining patterns consistent with the transcription-associated functions of PRAME signaling pathways in tumor cell populations.
A recombinant rabbit monoclonal clone PRAME/6928R antibody can be used for studies examining cancer-testis antigen biology and tumor-associated immune regulation pathways. Researchers studying broader melanoma biology, tumor immunology, and PRAME-associated signaling pathways may also be interested in our PRAME Antibody / Tumor Immunology Marker page featuring validated immunohistochemistry and western blot applications for cancer-testis antigen research.
Researchers studying melanoma-associated antigens, cancer-testis antigen biology, and tumor-associated immune signaling pathways may also be interested in our PRAME Antibody / Tumor Immunology Marker page featuring validated immunohistochemistry and western blot applications for PRAME-associated cancer research.
Optimal dilution of the OIP-4 Antibody / Cancer-Testis Antigen should be determined by the researcher.
A recombinant partial protein sequence (within amino acids 100-509) from the human protein was used as the immunogen for the OIP-4 antibody.
Aliquot the OIP-4 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
PRAME antibody, Preferentially expressed antigen in melanoma antibody, Opa-interacting protein 4 antibody, Tumor immunology marker antibody, Melanoma antigen antibody
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