mProX™ Human JAK2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 JAK2 mutant Ba/F3-MPL cell line generation.
Quantification of human JAK2 cDNA levels was done, and no discernible variation was seen between the four cell lines when the levels were normalized using endogenous mouse Jak2 cDNA levels. Western blot analysis was used to determine that all 4 cell lines had similar levels of total JAK2 and MPL protein.
Ref: Etheridge, S. Leah, et al. "A novel activating, germline JAK2 mutation, JAK2 R564Q, causes familial essential thrombocytosis." Blood, The Journal of the American Society of Hematology 123.7 (2014): 1059-1068.
Pubmed: 24381227
DOI: 10.1182/blood-2012-12-473777
Research Highlights
Although the crucial function of Janus kinase-2 (JAK2) in controlling myelopoiesis was recognized twenty years ago, JAK2's involvement in human illness was brought to light by the discovery of mutations in the pseudokinase domain of JAK2 in myeloproliferative neoplasms (MPNs) and other hematologic malignancies.
Silvennoinen, Olli, and Stevan R. Hubbard. "Molecular insights into regulation of JAK2 in myeloproliferative neoplasms." Blood, The Journal of the American Society of Hematology 125.22 (2015): 3388-3392.
Pubmed:
25824690
DOI:
10.1182/blood-2015-01-621110
These findings imply that when treating JAK2-amplified TNBCs, JAK2-specific inhibitors are more effective than dual JAK1/2 inhibitors. Moreover, JAK2 amplification may serve as a biomarker for JAK2 dependence, which may be utilized to identify individuals for JAK2 inhibitor clinical trials.
Balko, Justin M., et al. "Triple-negative breast cancers with amplification of JAK2 at the 9p24 locus demonstrate JAK2-specific dependence." Science translational medicine 8.334 (2016): 334ra53-334ra53.
Pubmed:
27075627
DOI:
10.1126/scitranslmed.aad3001