PhosphoSens ABL1 Protein Kinase Assays, Substrates & Recombinant Enzymes
Continuous, real-time assays that directly quantify ABL1 catalytic activity — generating a full progress curve in every well for IC₅₀, mechanism, and selectivity studies.
Real-time kinetic or TRF endpoint formats
Optimized substrates and assay-ready kits
Compatible with physiological ATP and cofactors
Designed for: drug discovery, lead optimization, and mechanistic kinase research teams
ABL1 (ABL proto-oncogene 1) is a non-receptor tyrosine kinase belonging to the Abl family, which includes ABL1 and ABL2 (ARG). Under normal physiological conditions, ABL1 activity is tightly regulated through intramolecular autoinhibition, with the SH3 and SH2 domains clamping the kinase domain in an inactive conformation. Activation occurs via displacement of this autoinhibitory clamp by upstream signals, scaffolding proteins, or oncogenic rearrangements. Key substrates include CRKL, STAT5, FAK, and the adaptor protein DOK1, linking ABL1 to cell proliferation, survival, cytoskeletal remodeling, and DNA damage response. In chronic myelogenous leukemia (CML) and a subset of acute lymphoblastic leukemias (ALL), the chromosomal translocation t(9;22) generates the BCR-ABL1 fusion oncoprotein, constitutively activating kinase activity and driving uncontrolled myeloid expansion. This makes ABL1 one of the most validated oncology drug targets in history, and the success of imatinib as a molecularly targeted therapy established the proof-of-concept for kinase inhibitor drug discovery across oncology.
Why PhosphoSens for ABL1?
Profiling ABL1 inhibitors presents several assay challenges: the kinase is frequently studied at physiological ATP concentrations to accurately capture competitive inhibitor potency, and the BCR-ABL1 fusion introduces complex regulatory dynamics that can confound endpoint measurements. Traditional ADP-Glo and HTRF assays require incubation stop points that miss transient kinetic phenomena such as slow-on/slow-off binding, covalent inactivation (kinact/KI), and induced-fit mechanisms critical for third-generation inhibitors like ponatinib and asciminib. Radiometric formats add safety and throughput limitations. AssayQuant's PhosphoSens continuous fluorescent assay monitors substrate phosphorylation in real time using physiological ATP, generating full progress curves that capture time-dependent inhibition, covalent kinact/KI parameters, and inhibitor mechanism of action without the endpoint artifacts that can misclassify allosteric STAMP inhibitors like asciminib.
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.
Wild-type and mutant forms of ABL1 for assay development, kinase profiling, and mechanistic studies.
Enzymes are supplied active and optimized for PhosphoSens® substrates.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Purity/Activity: For specific information on a given lot, see related technical data sheet.
Storage Conditions: Store product at -70°C. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
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Frequently Asked Questions: ABL1 Assays
Why is it important to use physiological ATP concentrations when profiling ABL1 inhibitors?
Most cellular ATP concentrations range from 1 to 5 mM, and competitive inhibitor IC50 values are highly sensitive to ATP concentration due to the Cheng-Prusoff relationship. Assays run at artificially low ATP levels can dramatically underestimate inhibitor potency relative to the cellular environment. AssayQuant PhosphoSens assays are validated at physiological ATP concentrations, providing IC50 and Ki values with direct translational relevance.
Can the PhosphoSens assay distinguish allosteric ABL1 inhibitors like asciminib from ATP-competitive inhibitors?
Yes. Because PhosphoSens generates continuous real-time progress curves, the kinetic signatures of allosteric inhibitors targeting the ABL1 myristoyl-binding pocket differ measurably from ATP-competitive mechanisms, enabling mechanistic classification. This is particularly valuable for characterizing STAMP inhibitors and combination inhibitor strategies where distinguishing mechanism of action is critical for lead optimization.
How does the PhosphoSens platform handle covalent or time-dependent ABL1 inhibitor characterization?
PhosphoSens continuously monitors phosphorylation over time, allowing direct observation of the time-dependent loss of enzyme activity characteristic of covalent or slow-binding inhibitors. From these progress curves, kinact and KI parameters can be extracted, which are not accessible from single-timepoint endpoint assays such as ADP-Glo or HTRF, making PhosphoSens essential for covalent ABL1 inhibitor programs.
Data & Resources
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.
Discover how continuous assay formats power deep understanding of kinase function. See how
PhosphoSens® assays guide inhibitor profiling, selectivity assessment, and
mechanistic characterization.