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BMX (Bone Marrow X-linked kinase), also known as ETK, is a non-receptor tyrosine kinase belonging to the Tec family, which includes BTK, ITK, TEC, and TXK. Like other Tec kinases, BMX contains an N-terminal pleckstrin homology (PH) domain, a Tec homology (TH) domain, SH3 and SH2 domains, and a C-terminal catalytic kinase domain. BMX is activated downstream of PI3K-generated PIP3, which recruits BMX to the plasma membrane via its PH domain, facilitating transphosphorylation at Y566 in the activation loop. Key substrates include STAT3, AKT, and FAK. BMX participates in PI3K/AKT, JAK/STAT, and androgen receptor signaling pathways. It is highly expressed in hematopoietic progenitors, endothelial cells, and epithelial tissues. BMX has been implicated in prostate cancer progression, acute myeloid leukemia (AML), glioblastoma, and inflammatory signaling. Its role in promoting tumor cell survival, invasion, and resistance to apoptosis makes BMX a compelling oncology drug target, particularly in castration-resistant prostate cancer and hematologic malignancies.
BMX presents several assay challenges in drug discovery: its requirement for physiological ATP concentrations (1-5 mM intracellularly) means that endpoint assays using low ATP can overestimate inhibitor potency, particularly for ATP-competitive compounds. ADP-Glo and HTRF detect single time-point signals, missing biphasic kinetics, substrate depletion artifacts, and covalent inhibitor mechanisms critical for BTK-class covalent probes targeting BMX C496. Radiometric assays add safety and throughput limitations. PhosphoSens continuous fluorescent assays use CSox-based peptide substrates to monitor BMX-catalyzed phosphorylation in real time at physiological ATP, generating full progress curves. This enables accurate Km(ATP) determination, detection of covalent kinact/KI parameters for irreversible inhibitors, and identification of time-dependent inhibition — all in a homogeneous, mix-and-read format compatible with high-throughput screening and mechanistic profiling.
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Ask Our Scientists →Continuous, real-time fluorescent assays optimized for quantitative BMX activity measurements, IC50 determination, and mechanistic studies.
PhosphoSens-Kinetic assays directly quantify enzyme activity by continuously monitoring substrate phosphorylation or dephosphorylation in real time, generating a full progress curve in every well.
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Kits
Ready-to-use assay kits containing substrate and all essential reagents.
Automatically save 10% when bundling 10ug recombinant enzyme with your 1,000 assay kit. View enzymes
Substrate
Bulk PhosphoSens® substrate for assay development and high-throughput workflows.
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Request a QuoteRobust endpoint TRF assays optimized for high-throughput screening and quantitative BMX activity measurement in plate-based workflows.
PhosphoSens-Red assays use europium-based time-resolved fluorescence detection to enable robust, plate-based quantification of enzyme activity, making them well suited for high-throughput screening workflows.
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Kits
Ready-to-use TRF assay kits containing substrate and essential reagents.
Automatically save 10% when bundling 10ug recombinant enzyme with your 1,000 assay kit. View enzymes
Substrate
Bulk substrate for PhosphoSens-Red TRF assays and high-throughput workflows.
Automatically save 10% when bundling Reagent Packs with your substrate. View Reagent Packs
Select a kit, substrate, or enzyme above. Our team will confirm pricing, availability, and any applicable bundle discounts.
Request a QuoteWild-type and mutant forms of BMX for assay development, kinase profiling, and mechanistic studies. Enzymes are supplied active and optimized for PhosphoSens® substrates.
Rat • Baculovirus-Insect Cells
Price: $$348.00
Request a QuotePhosphoSens uses proprietary CSox-containing peptide substrates that undergo a fluorescence change upon phosphorylation by BMX, enabling continuous monitoring of kinase activity without stopping the reaction. This generates full progress curves at each inhibitor concentration, providing richer kinetic data than endpoint methods. The approach is antibody-free, homogeneous, and compatible with both purified BMX and cell lysate formats.
Yes u2014 because PhosphoSens monitors phosphorylation continuously over time, it directly captures the time-dependent loss of BMX activity characteristic of covalent inhibitors targeting C496, the equivalent of the BTK C481 covalent warhead site. Full progress curve analysis allows extraction of kinact and KI parameters that endpoint assays cannot resolve. This is particularly valuable for profiling irreversible Tec family inhibitors under development for BMX-driven cancers.
BMX inhibitor potency is strongly influenced by ATP concentration because most small-molecule inhibitors compete with ATP for the kinase active site. Assays run at artificially low ATP concentrations overestimate inhibitor affinity relative to cellular conditions where ATP is present at 1-5 mM. PhosphoSens assays are validated at physiological ATP concentrations, ensuring that Ki and IC50 values better predict cellular and in vivo inhibitor efficacy.
Explore data and documents to support your kinase and phosphatase experiments. Download sample data, protocols and other resources to see how our assays perform and to help you get started in your own lab. All validation data generated using PhosphoSens® assays under recommended conditions.
Each validation report provides experimental conditions and data showing:
Protocol
See how the PhosphoSens-Kinetic Assay can be used to find the IC50 of a kinase inhibitor.
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Discover how continuous assay formats power deep understanding of kinase function. See how PhosphoSens® assays guide inhibitor profiling, selectivity assessment, and mechanistic characterization.
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Need broader selectivity data? KinSight profiling runs your compounds across our full kinase panel under identical PhosphoSens conditions.
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