mProX™ Human BLK Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Blk(Y501F) drives resistance to apoptosis and cytokine-independent proliferation.
IL-3 was not present throughout the culture of non-transfected Ba/F3 cells (NT), Ba/F3 Blk-wt, and Ba/F3 Blk(Y501F). The proportion of viable cells at various times is shown in the graph on the left, where each data point is the mean of a count of duplicate samples. The total number of live cells is represented on the graph to the right.
Ref: Petersen, D. L., et al. "B-lymphoid tyrosine kinase (Blk) is an oncogene and a potential target for therapy with dasatinib in cutaneous T-cell lymphoma (CTCL)." Leukemia 28.10 (2014): 2109-2112.
Pubmed: 24919804
DOI: 10.1038/leu.2014.192
Research Highlights
Many tyrosine kinases, including receptor and nonreceptor kinds, are involved in the etiology and medication resistance of almost all forms of leukemia in malignant hemopoiesis. Scientific literature has examined ABL1 kinase mutations and their pharmacological inhibitors in great detail.
K. Bhanumathy, Kalpana, et al. "Protein tyrosine kinases: their roles and their targeting in leukemia." Cancers 13.2 (2021): 184.
Pubmed:
33430292
DOI:
10.3390/cancers13020184
The non-receptor tyrosine kinase B-lymphoid tyrosine kinase (BLK) is a member of the SRC family of kinases. B-cell development and B-cell receptor signaling are known to be functionally impacted by BLK. According to recent data, B-lymphoid tyrosine kinase may be a possible oncogene in cutaneous T-cell lymphoma and other T-cell cancers, where it is expressed ectopically.
Petersen, David Leander, et al. "A novel BLK-induced tumor model." Tumor Biology 39.7 (2017): 1010428317714196.
Pubmed:
28670978
DOI:
10.1177/1010428317714196