| Code | CSB-RA126181A0HU |
| 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 |
MCM2 serves as an essential component of the pre-replicative complex, functioning as a DNA helicase that unwinds double-stranded DNA during S phase to enable faithful genome duplication. As a licensing factor, MCM2 ensures that DNA replication occurs only once per cell cycle, making it a valuable marker for studying cell proliferation, cancer biology, and DNA damage response pathways.
This recombinant monoclonal antibody, generated from clone 7D10, offers the reproducibility and consistency that demanding research applications require. Because the antibody sequence is defined and produced recombinantly in rabbit host, you can expect uniform performance across experiments and between lots, eliminating the variability often encountered with traditional hybridoma-derived reagents.
Validation across multiple platforms demonstrates this antibody's versatility in your experimental workflows. Western blot analysis successfully detects MCM2 in human cell lines including Jurkat, Raji, and HL-60, as well as mouse NIH/3T3 cells, confirming cross-species reactivity. The observed band at approximately 130 kDa runs higher than the predicted 102 kDa molecular weight, which likely reflects post-translational modifications such as phosphorylation or glycosylation that are characteristic of this heavily regulated protein. Immunohistochemistry staining has been validated in human cervical cancer and testis tissue sections, revealing nuclear localization patterns consistent with MCM2's role in replication licensing. Additional validation in HeLa cells by immunofluorescence and Jurkat cells by flow cytometry provides flexibility for both imaging and quantitative single-cell analysis approaches.
Whether investigating replication stress, characterizing proliferative indices in tumor samples, or exploring cell cycle regulation, this antibody delivers reliable MCM2 detection across diverse experimental contexts.
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