ONECUT1 antibodies are widely used to study:
Pancreatic Development: ONECUT1 regulates pancreatic progenitor differentiation by priming enhancers of genes like NKX6.1, NEUROG3, and PDX1, which are essential for β-cell maturation .
Diabetes Mechanisms: Pathogenic ONECUT1 mutations impair β-cell development and are linked to neonatal diabetes and type 2 diabetes (T2D) .
Liver Function: ONECUT1 modulates liver-expressed genes, including those involved in glucose homeostasis and drug metabolism .
Western Blot: Anti-ONECUT1 antibodies detect bands at 51–60 kDa, consistent with its theoretical molecular weight (~51 kDa). For example, PA2214 identifies ONECUT1 in HepG2 (human), RH35 (rat), and mouse liver lysates .
Immunocytochemistry (ICC): AF6277 localizes ONECUT1 to nuclei and cytoplasm in HepG2 cells, confirming its role as a nuclear transcription factor .
Immunohistochemistry (IHC): Proteintech’s 25137-1-AP shows strong staining in human liver cancer tissues, supporting ONECUT1’s oncogenic associations .
Binds to enhancers of FOXA2, PROX1, and SOX9 during pancreatic progenitor differentiation, facilitating endocrine specification .
Cooperates with PDX1 and GATA6 to activate β-cell-specific programs, with disruptions causing pancreatic hypoplasia .
Rare ONECUT1 missense variants (e.g., p.P75A) are implicated in T2D susceptibility .
Biallelic mutations cause neonatal syndromic diabetes, while monoallelic variants contribute to MODY-like phenotypes .
Cross-Reactivity: Some antibodies (e.g., PA2214) show no cross-reactivity with non-target proteins, while others (e.g., 25137-1-AP) may require species-specific validation .
Cell-Type Specificity: Bulk sequencing data may obscure heterogeneous cell populations, necessitating single-cell analyses for precise mechanistic insights .