mProX™ Human DYRK3 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 DYRK3 phosphorylates SNAPIN at the threonine 14 residue.
Following a 24-hour transfection of HEK293 cells with a plasmid encoding Myc-SNAPIN, three identical cell lysates were subjected to immunoprecipitation using an anti-Myc antibody. Through immunoblotting with an anti-Myc antibody, the correct expression of transiently produced SNAPIN in cell extracts was confirmed (Input).
Ref: Lee, Ye Hyung, et al. "DYRK3 phosphorylates SNAPIN to regulate axonal retrograde transport and neurotransmitter release." Cell Death Discovery 8.1 (2022): 503.
Pubmed: 36585413
DOI: 10.1038/s41420-022-01290-0
Research Highlights
By controlling the activity of a crucial enzyme involved in condensate disintegration and translation restoration, Hsp90 establishes a connection between stress adaption and cell development.
Mediani, Laura, et al. "Hsp90-mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling." EMBO reports 22.5 (2021): e51740.
Pubmed:
33738926
DOI:
10.15252/embr.202051740
The prognosis for patients with glioblastoma multiforme (GBM), a malignant primary brain tumor, is not good. Even though surgery, chemotherapy, and radiation therapy are the usual treatments for gastric cancer of the breast (GBM), a tiny percentage of tumor cells that survive develop resistance to treatment and become more aggressive.
Kim, Kyeongmin, et al. "Dual specificity kinase DYRK3 promotes aggressiveness of glioblastoma by altering mitochondrial morphology and function." International Journal of Molecular Sciences 22.6 (2021): 2982.
Pubmed:
33804169
DOI:
10.3390/ijms22062982