mProX™ Human CLK2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
Made to Order Inquiry
InquiryProduct Information
Product Properties
Protocols
Please visit our protocols page.
Customer Reviews
Dorothy
Verified Customer
Barbara
Verified Customer
Any questions about our products? Please visit our frequently asked questions page.
Published Data
Fig.1 CLK2 had a high expression in NSCLC tissues and cell lines.
qRT-PCR revealed a substantial increase in CLK2 expression in 32 lung cancer cases' tissues as compared to the control group. When comparing stage III-IV lung cancer patients to those in stage I-II, there was a significant increase in CLK2 expression.
Ref: Liu, Bing, et al. "CLK2 promotes occurrence and development of non-small cell lung cancer." Journal of the Balkan Union of Oncology 26.1 (2021): 58-64.
Pubmed: 33721432
Research Highlights
These findings suggest that EMT splicing pattern modulation and growth inhibition of breast tumors may be achieved by therapeutic targeting of CLK2.
Yoshida, Taku, et al. "CLK2 is an oncogenic kinase and splicing regulator in breast cancer." Cancer research 75.7 (2015): 1516-1526.
Pubmed:
25670169
DOI:
10.1158/0008-5472.CAN-14-2443
A significant risk of autism spectrum disorder (ASD) is one of the neurological hallmarks of Phelan-McDermid syndrome (PMDS), which is caused by SH3 and multiple ankyrin repeat domains 3 (SHANK3) haploinsufficiency.
Bidinosti, Michael, et al. "CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency." Science 351.6278 (2016): 1199-1203.
Pubmed:
26847545
DOI:
10.1126/science.aad5487