| Code | CSB-RA015270MA1HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:2000 |
| FC | 1:50-1:200 |
MYC stands as one of the most extensively studied oncogenes in cancer biology, encoding a transcription factor that orchestrates cellular proliferation, growth, and metabolism. Dysregulation of MYC expression drives tumorigenesis across a remarkable spectrum of human malignancies, making it an essential target for researchers investigating cell cycle control, oncogenic signaling pathways, and therapeutic vulnerabilities in cancer cells.
This recombinant monoclonal antibody against human MYC offers the reproducibility that demanding research applications require. Generated through recombinant technology with a defined sequence, the antibody delivers consistent performance across experiments and eliminates the lot-to-lot variability that can compromise longitudinal studies. The human IgG1 isotype format, combined with affinity chromatography purification, ensures high specificity for your target while minimizing background interference.
Validation studies demonstrate robust performance across multiple experimental platforms. In western blot applications, the antibody reliably detects MYC protein across a diverse panel of human cell lines including K562, PC-3, HepG2, HeLa, Jurkat, A549, and HEK293 lysates at dilutions ranging from 1:500 to 1:2000. The observed band at 56 kDa, slightly higher than the predicted 51 kDa molecular weight, reflects post-translational modifications including phosphorylation events known to regulate MYC stability and activity. Flow cytometry validation in K562 cells confirms the antibody's utility for intracellular detection of MYC protein with clear separation from isotype control, supporting quantitative analysis of MYC expression at the single-cell level.
Whether investigating MYC-driven transcriptional programs, screening for pathway inhibitors, or characterizing tumor cell populations, this antibody provides a reliable tool for advancing your understanding of this critical oncogenic regulator.
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