Creative Biolabs offers a highly sensitive and versatile HDAC Assay Service to support functional analysis, compound screening, and pathway interrogation in immuno-oncology settings. Our platform allows precise measurement of HDAC class I, II, and IV isoforms using enzymatic and cell-based models.
Histone deacetylases (HDACs) are a family of epigenetic enzymes that remove acetyl groups from lysine residues on histone and non-histone proteins, profoundly altering chromatin structure and gene expression. In the context of cancer immunology, HDACs suppress key immune signaling pathways, including MHC class I/II expression, immune checkpoint regulation, cytokine production, and T cell activation. Dysregulated HDAC activity is implicated in immune escape, immune cell exhaustion, and poor antigen presentation in tumors.
We offer HDAC assays tailored for studying immune-associated gene regulation, epigenetic drug discovery, and mechanistic screening:
Scalable formats for screening HDAC inhibitors with Z' > 0.8 and robust assay performance metrics
A1: Yes. We offer isoform-specific detection using selective inhibitors, substrates, or antibody-based readouts for class I, II, and IV HDACs.
A2: We analyze changes in MHC I/II expression, checkpoint molecule transcription, and cytokine levels using flow cytometry, qPCR, and ELISA following HDAC inhibition in immune cells or tumor models.
A3: Absolutely. We provide dose–response profiling, IC₅₀ determination, and mechanism-of-action studies for HDAC-targeted compounds.
A4: Yes. We can test HDAC inhibitor effects in specific immune contexts such as exhausted CD8⁺ T cells or M1/M2 macrophage models.
A5: Yes, we support both primary PBMC-derived subsets and established immune cell lines for HDAC profiling.
Creative Biolabs provides advanced HDAC profiling solutions to support your immuno-oncology discovery programs. Whether you're exploring epigenetic reprogramming, immune enhancement, or HDAC-targeted drug candidates, our expert team offers full technical support and customized workflows.