| Code | CSB-RA972223A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| FC | 1:50-1:200 |
BRD2 belongs to the bromodomain and extra-terminal (BET) family of epigenetic readers, recognizing acetylated lysine residues on histones to regulate transcription, cell cycle progression, and chromatin remodeling. As a key mediator linking histone modifications to gene expression, BRD2 has emerged as a significant target in cancer biology, inflammatory disease research, and studies of transcriptional regulation. Its role in recruiting transcriptional machinery to acetylated chromatin makes it particularly relevant for researchers investigating epigenetic mechanisms and therapeutic interventions targeting BET proteins.
This recombinant monoclonal antibody, clone 3C6, offers the reproducibility and consistency that demanding epigenetic research requires. Generated against a synthesized peptide from human BRD2, the antibody is produced using recombinant technology, ensuring sequence-defined specificity and eliminating the lot-to-lot variability that can compromise longitudinal studies or multi-site collaborations. Affinity chromatography purification delivers a reagent suitable for quantitative applications where signal reliability is essential.
Validation for flow cytometry demonstrates robust detection of BRD2 in HeLa cells, with clear separation from isotype control when used at 1:100 dilution. The protocol employed fixation and permeabilization to access this nuclear target, with acquisition of over 10,000 events confirming statistically meaningful detection. Recommended working dilutions of 1:50 to 1:200 for flow cytometry provide flexibility for optimization across different experimental conditions. The antibody is also validated for ELISA applications.
This reagent supports investigations into BET protein function, chromatin biology, and the growing field of epigenetic drug discovery, where reliable detection of bromodomain-containing proteins is fundamental to understanding therapeutic mechanisms.
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