This gene encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. The encoded protein is a Ca2+-permeable, nonselective cation channel that is thought to be involved in the regulation of systemic osmotic pressure. Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC. Multiple transcript variants encoding different isoforms have been found for this gene.
The use of this Antibodies
has been cited in the following citations:
Photobiomodulation with 630-nm LED radiation inhibits the proliferation of human synoviocyte MH7A cells possibly via TRPV4/PI3K/AKT/mTOR signaling pathway,Meng, C;Xia, Q;Wu, H;Huang, H;Liu, H;Li, Y;Zhang, F;Song, W;,Lasers Med Sci 2020,PubMed ID 32162133[TRPV4]
beta Actin Mouse Monoclonal Antibody, Clone OTI1, Loading Control
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