The antibody has been pivotal in elucidating C12orf43’s role in breast cancer chemoresistance:
Mechanism: C12orf43 interacts with NAT10, an enzyme responsible for N4-acetylcytidine (ac4C) RNA modification. This interaction stabilizes BMI1 mRNA, leading to P53 ubiquitination and degradation, thereby promoting tumor progression .
Experimental Techniques:
While primarily studied in oncology, C12orf43 has been linked to coronary artery disease in genetic association studies . The antibody may aid in investigating its role in vascular pathologies.
Quercetin Synergy: The antibody has been used to validate quercetin’s disruption of the C12orf43/NAT10 interaction, which reverses doxorubicin (ADM) resistance in breast cancer models .
Diagnostic Utility: Elevated C12orf43 expression correlates with chemoresistance, positioning it as a potential biomarker for personalized therapy .
Specificity: Cross-reactivity with orthologs (e.g., mouse: 69%, rat: 58%) requires careful validation in non-human studies .
Clinical Translation: No approved therapeutic applications yet; preclinical data focus on mechanistic insights .
| Format | Advantages | Limitations |
|---|---|---|
| Biotin-conjugated | Enhanced sensitivity in ELISA; cost-effective | Limited to ELISA and avidin-based assays |
| Unconjugated | Versatile for Western blotting, Co-IP | Requires secondary antibody labeling |