| Code | CSB-RA020519MA1HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:2000 |
| IF | 1:50-1:200 |
| FC | 1:50-1:200 |
Ribonucleoside-diphosphate reductase subunit M2 (RRM2) serves as an essential component of the ribonucleotide reductase enzyme complex, which catalyzes the rate-limiting step in deoxyribonucleotide synthesis required for DNA replication and repair. As a tightly regulated cell cycle protein with expression peaking during S phase, RRM2 has emerged as a significant focus in cancer biology and epigenetics research, where its dysregulation correlates with tumor progression and therapeutic resistance.
This recombinant monoclonal antibody (clone 14F4) offers researchers the consistency and reproducibility that sequence-defined production provides. Generated against recombinant human RRM2 protein and expressed as a human IgG1 isotype, this antibody delivers lot-to-lot uniformity critical for longitudinal studies and quantitative comparisons across experiments.
Validation data demonstrates reliable performance across multiple experimental platforms. Western blot analysis of A-431 whole cell lysate detects a band at the predicted molecular weight of 45 kDa, confirming target specificity at dilutions between 1:500 and 1:2000. Immunofluorescence studies in both HeLa and HepG2 cells reveal clear cytoplasmic localization patterns consistent with RRM2's known subcellular distribution, with effective staining achieved at 1:30 dilution. Flow cytometry analysis using Jurkat cells shows distinct positive population shifts compared to isotype controls, enabling quantitative assessment of RRM2 expression at the single-cell level.
The antibody's compatibility with ELISA, Western blot, immunofluorescence, and flow cytometry provides workflow flexibility for researchers investigating RRM2 in contexts ranging from cell cycle regulation to nucleotide metabolism. This versatility makes it particularly valuable for studies in epigenetics and nuclear signaling where RRM2 function intersects with DNA synthesis pathways.
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