RPL7A is a conserved ribosomal protein encoded by the RPL7A gene (NCBI Gene ID: 6130) and is essential for ribosome assembly and translational fidelity . Beyond its canonical role, RPL7A interacts with nuclear hormone receptors (e.g., thyroid hormone receptor, retinoic acid receptor) to regulate gene expression and cellular differentiation .
| Property | Details |
|---|---|
| Molecular Weight | ~30 kDa (observed: 30–32 kDa) |
| Gene Location | Chromosome 9q34.2 (human) |
| Protein Function | Ribosome assembly, translation regulation, cell growth, and differentiation |
RPL7A antibodies are widely used in basic and clinical research. Their applications include:
Western Blot (WB): Detects RPL7A at ~30 kDa in human, mouse, and rat samples .
Immunohistochemistry (IHC): Localizes RPL7A in formalin-fixed tissues (e.g., lung carcinoma, breast cancer) .
Immunofluorescence (IF): Visualizes RPL7A in cytoplasmic and nucleolar compartments .
Immunoprecipitation (IP): Isolates RPL7A-protein complexes (e.g., ribosomal subunits) .
Recommended Dilutions:
RPL7A antibodies exhibit high specificity across species and experimental conditions:
Depletion of RPL7A disrupts 60S subunit assembly, impairing rRNA processing and Ty1 retrotransposon mobility in yeast .
In Alzheimer’s disease, RPL7A dysfunction correlates with ribosome stalling and toxic APP fragment accumulation .
Upregulating RPL7A in injured RGCs promotes axon regeneration and neuronal survival in murine models .
Anti-RPL7A autoantibodies are implicated in systemic lupus erythematosus (SLE) diagnostics. Panels combining anti-RPL7A with anti-RPLP2 and anti-PARP1 improve SLE detection specificity .