At Creative Biolabs, our KAT Assay Service provides a reliable platform for assessing the enzymatic activity of KAT family members and their roles in immune-modulated cancer pathways. Our service supports drug discovery, target validation, and mechanistic research in epigenetic immunology.
Lysine acetyltransferases (KATs), also known as histone acetyltransferases (HATs), catalyze the transfer of acetyl groups to lysine residues on histones and non-histone proteins. This epigenetic modification opens chromatin for transcriptional activation and regulates numerous immune-related processes, including cytokine production, antigen processing, and T cell differentiation. In the tumor microenvironment, dysregulated KAT activity may enhance tumor immune evasion by altering gene expression involved in immune recognition or by modulating immune cell phenotype.
We offer robust solutions to detect, quantify, and characterize the functional activities of major KAT family enzymes, including CBP/p300, GCN5, PCAF, and Tip60:
Quantitative detection of acetyl group transfer to peptide or protein substrates using fluorescent detection reagents
High-sensitivity incorporation of ³H-acetyl-CoA onto lysine residues of synthetic or native substrates
Antibody-based readouts of global or site-specific histone/non-histone protein acetylation (e.g., Ac-H3K27, Ac-p53)
Use of reconstituted nucleosomes or isolated chromatin for functional relevance in immune gene activation studies
Measurement of transcriptional outcomes of KAT inhibition on genes related to antigen presentation, interferon response, and T cell co-stimulation
Assays adaptable to 96/384-well screening for epigenetic modulator libraries with validated controls
A1: Yes. We offer both isoform-specific assays and selective inhibitors to distinguish between CBP/p300, GCN5, and Tip60 activities.
A2: Yes. We can measure KAT activity or acetylation effects in tumor-infiltrating immune cells, dendritic cells, or macrophage systems.
A3: We provide downstream transcriptional profiling using qPCR arrays for genes involved in MHC expression, checkpoint regulation, and interferon signaling.
A4: Yes. We can deliver IC₅₀, Km, and Vmax data using multiple detection platforms to characterize compound–enzyme interactions.
A5: Absolutely. Our platform is optimized for screening libraries targeting immune-related transcriptional activation via histone acetylation.
At Creative Biolabs, we help scientists explore how KAT enzymes regulate immune responses within the tumor microenvironment. Our tailored assay solutions are designed to uncover novel immune-epigenetic interactions and accelerate immunomodulator discovery.