The MAGEC2 Antibody is available in two primary forms: polyclonal and monoclonal. Key specifications include:
Both antibodies are validated for human samples, with the polyclonal version optimized for tissue-based assays and the monoclonal version suited for biochemical techniques like immunoprecipitation.
The antibody has been instrumental in elucidating MAGEC2’s role in oncogenesis:
OS: High expression → median survival = 20.3 months (P = 0.0048).
RFS: High expression → median survival = 14.5 months (P = 0.036).
Tumor Growth Promotion: Knockdown of MAGEC2 via shRNA in HCC cell lines (e.g., MHCC97H) reduced xenograft tumor size by 60% compared to controls (P = 0.002) .
Epithelial-to-Mesenchymal Transition (EMT): MAGEC2 knockdown increased epithelial markers (E-cadherin) and decreased mesenchymal markers (N-cadherin, fibronectin), suggesting its role in promoting metastasis .
Protein Interactions: MAGEC2 interacts with TRIM28 (a ubiquitin ligase) and TAF9 (a transcription coactivator), stabilizing its expression and facilitating oncogenic signaling .
Biomarker Potential: Elevated MAGEC2 expression has been linked to aggressive phenotypes in breast, lung, and melanoma cancers, making it a candidate for diagnostic panels .
Immunotherapy Target: As a CTA, MAGEC2 is under investigation for vaccine development and adoptive T-cell therapies. Early-phase trials (e.g., MAGE-C2 peptide vaccines) have shown safety and immune responses in cancer patients .
Heterogeneity in Expression: Regional and racial differences in MAGEC2 expression (higher in East Asian HCC cohorts) necessitate diverse patient sampling in trials .
Mechanistic Gaps: The exact signaling pathways downstream of MAGEC2 (e.g., Cyclin E regulation, apoptosis inhibition) remain understudied .