| Code | CSB-RA898865A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:2000 |
| IHC | 1:50-1:200 |
| IF | 1:50-1:200 |
| FC | 1:50-1:200 |
RAB7A is a small GTPase that serves as a master regulator of late endosomal and lysosomal trafficking, playing essential roles in autophagy, endosome maturation, and lysosomal biogenesis. Its involvement in cellular degradation pathways makes it a critical target for researchers investigating neurodegenerative diseases, cancer progression, and metabolic disorders where vesicular trafficking is disrupted.
This recombinant rabbit monoclonal antibody, clone 15A6, offers the consistency and reproducibility that demanding experimental workflows require. Because it is produced from a defined sequence rather than traditional hybridoma methods, you can expect reliable lot-to-lot performance across long-term studies and multi-site collaborations. The antibody was raised against a synthetic peptide derived from human RAB7A and demonstrates cross-species reactivity with both human and rat samples.
Validation data confirms robust performance across multiple applications. In western blot experiments, the antibody detects a clean band at the predicted 23 kDa molecular weight across diverse human cell lines including U-87MG, PC-3, A549, HeLa, A431, and HT-29, as well as rat brain tissue lysate, providing confidence when working with different model systems. Immunohistochemical staining has been validated in paraffin-embedded human liver cancer and stomach tissue sections using citrate buffer antigen retrieval. For cellular localization studies, immunofluorescence staining in A431 cells and flow cytometry analysis in K562 cells demonstrate clear signal with appropriate controls.
Whether you are characterizing autophagy flux, investigating endolysosomal dysfunction in disease models, or examining RAB7A expression patterns in tumor samples, this antibody provides the versatility and reliability needed for publication-quality results across your experimental platforms.
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