Protein phosphatases (PPs) act as key regulators in the dynamic balance of protein phosphorylation, reversing the actions of kinases and fine-tuning intracellular signaling. In immune regulation and cancer, phosphatases such as PP1, PP2A, and SHP2 (PTPN11) are known to influence T cell receptor (TCR) signaling, immune checkpoint signaling (e.g., PD-1/PD-L1), and cytokine responsiveness.
Aberrant phosphatase activity contributes to tumor immune evasion by dampening effector T cell function or promoting immune suppressive environments. Inhibiting or modulating PP activity has emerged as a novel strategy to restore anti-tumor immune responses. To support these investigations, Creative Biolabs offers comprehensive PP assay services focused on phosphatase kinetics, activity screening, and immune response correlation.
We provide a versatile set of services targeting serine/threonine and tyrosine phosphatases, enabling detailed functional and mechanistic evaluations:
Measure dephosphorylation of pNPP or phosphopeptides via absorbance at 405 nm; useful for endpoint or kinetic analysis.
Utilize fluorogenic phospho-substrates for continuous-read formats; ideal for high-throughput platforms.
Evaluate endogenous or recombinant phosphatase modulation through western blot or flow cytometry-based phospho-specific antibodies.
T cell activation, cytokine profiling, or cytotoxicity assays in co-culture systems following phosphatase inhibitor treatment.
HTS-compatible enzyme-based assays with IC₅₀ determination and functional follow-up.
Identify preferred phospho-substrates of PP isoforms via peptide libraries or proteomics analysis.
Our assays cover major phosphatase families including PP1, PP2A, PTPN11 (SHP2), DUSP family, and calcineurin, all of which are functionally relevant in immune escape and tumor progression.
A1: SHP2 (PTPN11) and PP2A are heavily implicated in inhibiting T cell signaling and promoting immune escape in solid tumors.
A2: Yes. We support both lysate-based and intact cell assays, including phospho-flow cytometry and immune activation readouts.
A3: Certainly. We can measure T cell proliferation, IFN-γ release, PD-1 expression, or cytotoxicity post-treatment.
A4: Yes, our platform supports experiments in primary PBMCs, CD8+ T cells, macrophages, and tumor co-cultures.
A5: We offer phospho-peptide substrate libraries and recombinant protein assays to validate isoform-specific activity.
At Creative Biolabs, we specialize in bridging enzymatic assay precision with immunological relevance. Our PP assay service empowers oncology researchers to uncover how phosphatase modulation reshapes immune signaling and enhances therapeutic strategies.