ILF3 antibodies target the protein encoded by the ILF3 gene, which plays dual roles in transcriptional regulation and post-transcriptional RNA stabilization . These antibodies are critical for:
Detecting ILF3 expression in tissues (e.g., cancer vs. normal)
Characterizing subcellular localization (nuclear vs. cytoplasmic)
Validating ILF3 knockdown/overexpression in experimental models
Gastric Cancer (GC):
ILF3 protein overexpression was observed in 72.5% of GC tissues vs. 13.75% in adjacent mucosa (χ²=48.89; P<0.001) .
siRNA-mediated ILF3 suppression reduced GC cell viability by 38.6% (BGC823) and 41.8% (SGC7901) at 48 hours :
| Cell Line | Viability (% vs Control) | G0/G1 Phase Increase | p21 Upregulation |
|---|---|---|---|
| BGC823 | 61.4% | +18.7% | 3.2-fold mRNA |
| SGC7901 | 58.2% | +15.9% | 2.8-fold mRNA |
Dendritic Cell Regulation:
ILF3 antibodies confirmed its role as a negative regulator of DC maturation, with NF110's DZF domain being critical for suppressing innate immune responses .
ILF3 antibodies helped identify its pro-angiogenic function through VEGF-induced mRNA stabilization in endothelial cells .
Western Blot Sensitivity: