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ABL1 Kinase Assay

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Compound Test Services

CT-001

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Product Description


ABL1, also known as c-Abl, is a member of the non‑receptor tyrosine kinase family that plays a critical role in cell proliferation, differentiation, apoptosis, and cytoskeletal regulation. ABL1 is best characterized by its involvement in the BCR‑ABL1 fusion oncoprotein, resulting from a chromosomal translocation that drives the pathogenesis of chronic myeloid leukemia (CML) and Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL). Beyond its role in hematological malignancies, dysregulation of ABL1 signaling has been implicated in solid tumors, neurodegenerative disorders, and inflammatory diseases. The central role of ABL1, particularly in BCR‑ABL1-driven leukemogenesis, has established it as a highly validated target for cancer therapy, leading to the successful development of tyrosine kinase inhibitors such as imatinib and next‑generation agents for resistant mutations.


Screeningbio’s ABL1 Kinase Assay Kit provides a robust, sensitive, and high-throughput platform for quantifying ABL1 kinase activity and evaluating the potency of tyrosine kinase inhibitors (TKIs).


This kit utilizes the ADP-Glo Kinase Assay platform, a luminescent technology that measures the amount of ADP produced during the kinase reaction.

The assay is performed in two distinct steps:

  1. Kinase Reaction: ABL1 catalyzes the transfer of a phosphate group from ATP to a specific substrate, resulting in the production of phosphorylated substrate and ADP.

  2. ADP-Glo™ Reagent Addition: After the kinase reaction, the ADP-Glo™ Reagent is added to terminate the reaction and deplete any remaining unreacted ATP.

  3. Kinase Detection: The Kinase Detection Reagent is added to simultaneously convert the produced ADP back into ATP, which is then used by luciferase to generate a luminescent signal.

The light intensity produced is directly proportional to the ADP concentration and, consequently, to the enzymatic activity of the ABL1 kinase.



Data

TKs Kinase Inhibition Assay. Staurosporine was titrated using established assay protocol. Non-linear regression was used to plot RLU signal vs. [Compound, M], and EC50 /IC50 values were determined, using GraphPad Prism software.
TKs Kinase Inhibition Assay. Staurosporine was titrated using established assay protocol. Non-linear regression was used to plot RLU signal vs. [Compound, M], and EC50 /IC50 values were determined, using GraphPad Prism software.


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