mProX™ Human JAK1 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 JAK1 mutation, protein levels and IFNγ response in endometrial cancer cell lines.
According to JAK1 truncating p. K860fs mutation and JAK1 protein loss, immunoblot demonstrating downstream STAT1 activation, activating Y701 phosphorylation and HLA class I heavy chain levels in response to recombinant IFNγ (75 ng/ml for 16 hours) in endometrial cancer cell lines. The conventional molecular weights are displayed to the right of the panels.
Ref: Glaire, Mark A., et al. "Discordant prognosis of mismatch repair deficiency in colorectal and endometrial cancer reflects variation in antitumour immune response and immune escape." The Journal of pathology 257.3 (2022): 340-351.
Pubmed: 35262923
DOI: 10.1002/path.5894
Research Highlights
Cytokines that rely on JAK1 signaling to support receptor activator of NF-κB ligand production in osteoblasts and T cells-thereby promoting osteoclastogenesis-are also necessary for maintaining bone homeostasis. Here, it's unclear how much JAK1 contributes in comparison to other kinases.
Spinelli, Francesca Romana, Robert A. Colbert, and Massimo Gadina. "JAK1: Number one in the family; number one in inflammation?." Rheumatology 60.Supplement_2 (2021): ii3-ii10.
Pubmed:
33950229
DOI:
10.1093/rheumatology/keab024
Our results show that in two mouse models of HLH, the deleterious effects of macrophage overactivation are suppressed by ruxolitinib at clinically relevant levels. The findings might be easily applied to the treatment of primary and possibly even secondary types of HLH in the clinic.
Maschalidi, Sophia, et al. "Therapeutic effect of JAK1/2 blockade on the manifestations of hemophagocytic lymphohistiocytosis in mice." Blood, The Journal of the American Society of Hematology 128.1 (2016): 60-71.
Pubmed:
27222478
DOI:
10.1182/blood-2016-02-700013