| Application | Recommended Dilution |
|---|---|
| IHC | 1:50-1:500 |
| IF | 1:30-1:200 |
Histone H1.4, encoded by the HIST1H1E gene, serves as a linker histone that plays a fundamental role in chromatin compaction and gene regulation. Phosphorylation at threonine 17 represents a dynamic post-translational modification that influences chromatin structure during cell cycle progression and transcriptional regulation, making it a valuable marker for researchers investigating epigenetic mechanisms and nuclear signaling pathways.
This recombinant monoclonal antibody, clone 3E1, offers the reproducibility and consistency that demanding epigenetic studies require. Produced using recombinant technology with a sequence-defined approach, it eliminates the lot-to-lot variability that can compromise longitudinal studies or multi-site collaborations. The rabbit IgG format, purified by affinity chromatography, ensures high specificity for the phosphorylated threonine 17 epitope on human Histone H1.4.
Validation across multiple experimental platforms demonstrates this antibody's versatility in your workflow. Immunohistochemistry studies have confirmed reliable nuclear staining in paraffin-embedded human lymph node and pancreatic tissues using citrate buffer antigen retrieval at dilutions of 1:100, with a recommended working range of 1:50 to 1:500. For immunofluorescence applications, testing in MCF-7 human breast cancer cells at 1:56 dilution revealed clear nuclear localization patterns when counter-stained with DAPI, supporting its utility in cell-based epigenetic studies with recommended dilutions between 1:30 and 1:200.
Whether you are mapping phospho-histone dynamics during cell division, investigating chromatin remodeling in cancer models, or exploring transcriptional regulation mechanisms, this antibody provides a dependable tool for detecting this specific phosphorylation event in human samples across tissue-based and cellular immunostaining applications.
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