mProX™ Human P2RY6 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR 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
Alexander
Verified Customer
Harper
Verified Customer
Any questions about our products? Please visit our frequently asked questions page.
Published Data
Fig.1 The invalidation of the P2ry6 gene modulates AKT signaling.
Mice treated with AOM-DSS according to the instructions or control animals left untreated had their distal colons isolated. Western blots were used to analyze the expression of -catenin, AKT, and AKT phosphorylation on Thr308. To guarantee comparable protein loading and lysate integrity, GAPDH expression was employed.
Ref: Placet, Morgane, et al. "The G protein-coupled P2Y6 receptor promotes colorectal cancer tumorigenesis by inhibiting apoptosis." Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1864.5 (2018): 1539-1551.
Pubmed: 29454075
DOI: 10.1016/j.bbadis.2018.02.008
Research Highlights
Through the modification of the Hippo/YAP and Wnt/β-catenin signaling pathways, P2RY6 is a significant positive regulator of skin carcinogenesis.
Xu, Peng, et al. "P2RY6 has a critical role in mouse skin carcinogenesis by regulating the YAP and β-catenin signaling pathways." Journal of Investigative Dermatology 142.9 (2022): 2334-2342.
Pubmed:
35304248
DOI:
10.1016/j.jid.2022.02.017
This study provided fresh insight into the precise pro-inflammatory role that P2RY6-mediated signaling plays in neuroinflammation, which may open up new possibilities for the management of inflammatory reactions in the brain.
Timmerman, Raissa, Ella A. Zuiderwijk-Sick, and Jeffrey J. Bajramovic. "P2Y6 receptor-mediated signaling amplifies TLR-induced pro-inflammatory responses in microglia." Frontiers in Immunology 13 (2022): 967951.
Pubmed:
36203578
DOI:
10.3389/fimmu.2022.967951