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TRPV3 product belongs to a family of nonselective cation channels that function in a variety of processes, including temperature sensation and vasoregulation. Additionally we are shipping Transient Receptor Potential Cation Channel, Subfamily V, Member 3 Proteins (8) and Transient Receptor Potential Cation Channel, Subfamily V, Member 3 Kits (3) and many more products for this protein.
Showing 10 out of 195 products:
Human Polyclonal TRPV3 Primary Antibody for EIA, IHC (p) - ABIN356905
Frederick, Buck, Matson, Cortright: Increased TRPA1, TRPM8, and TRPV2 expression in dorsal root ganglia by nerve injury. in Biochemical and biophysical research communications 2007
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Human Monoclonal TRPV3 Primary Antibody for AA, ICC - ABIN863127
Masamoto, Kawabata, Fushiki: Intragastric administration of TRPV1, TRPV3, TRPM8, and TRPA1 agonists modulates autonomic thermoregulation in different manners in mice. in Bioscience, biotechnology, and biochemistry 2009
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Human Polyclonal TRPV3 Primary Antibody for EIA, IHC (p) - ABIN356906
Asakawa, Yoshioka, Matsutani, Hikita, Suzuki, Oshima, Tsukahara, Arimura, Horikawa, Hirasawa, Sakata: Association of a mutation in TRPV3 with defective hair growth in rodents. in The Journal of investigative dermatology 2006
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Human Monoclonal TRPV3 Primary Antibody for AA, ICC - ABIN361778
Xiao, Tang, Wang, Colton, Tian, Zhu: Calcium plays a central role in the sensitization of TRPV3 channel to repetitive stimulations. in The Journal of biological chemistry 2008
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The results of the present study show that polymorphism of TRPV3 contributed towards symptom severity in FM.
A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome in a Chinese family.
High Transient receptor potential vanilloid 3 protein expression could promote the proliferation of lung cancer cells. Transient receptor potential vanilloid 3 inhibition decreased [Ca2 (show CA2 Antibodies)+]i of lung cancer cells and cell cycle arrest at the G1/S boundary.
these data suggest that TRPV3 sparklets cause dilation of cerebral parenchymal arterioles by activating IK and SK channels in the endothelium
TRPV3 missense mutation identified as a cause of the rare Olmsted syndrome.
Hypoxia, FIH (show CASR Antibodies) inhibitors and mutation of asparagine 242 all potentiated TRPV3-mediated current, without altering TRPV3 protein levels, indicating that oxygen-dependent hydroxylation inhibits TRPV3 activity.
Using multiple sequence alignments as source for evolutionary, bioinformatics and statistical analysis, we have analyzed the evolutionary profiles for TRPV1 (show TRPV1 Antibodies), TRPV2 (show TRPV2 Antibodies), TRPV3 and TRPV4 (show TRPV4 Antibodies)
Study illustrates the antiadipogenic role of TRPV3 in the adipocytes.
this study provides powerful tools to broaden our understanding of ligand interaction with TRPV channels, and the availability of purified human TRPV3 opens up perspectives for further structural and functional studies
A mutation in TRPV3 causes focal palmoplantar keratoderma in a Chinese family.
TRPV3 is involved in the development of ear edema caused by arachinonic acid.
It was concluded that TRPV3 is expressed in a discrete subpopulation of vagal afferent neurons and may contribute to vagal afferent signaling either directly or in combination with TRPV1 (show TRPV1 Antibodies).
findings suggest that although TRPV3 agonism induces hypothermia in rodents, it may have a limited potential as a novel pharmacological method for induction of hypothermia
TRPV3 activation led to a decrease in embryonic stem cell proliferation. Cell cycle analysis revealed that TRPV3 activation increased the percentage of cells in G2/M phase.
In vivo evidence of a cooperative role between skin-derived TRPV3 and primary sensory neurons-enriched TRPV1 (show TRPV1 Antibodies) in modulation of moderate and noxious heat temperature sensation.
We found that NA indeed potentiated TRPV3 while inhibited TRPV2 (show TRPV2 Antibodies) and TRPV4 (show TRPV4 Antibodies)
Investigated the role of TRPV3 to wound healing using a tooth extraction model and found that oral wound closure was delayed in TRPV3KO compared with that in WT. TRPV3 mRNA was up-regulated in wounded tissues, so TRPV3 may contribute to oral wound repair.
Demonstrate similarities but also notable differences in TRPV3 pharmacology between recombinant and native systems.
a gain-of-function mutation in TRPV3 (TRPV3Gly573Ser) shows that increasing skin temperature is associated with the modulation of dermal dendritic cells
This gene product belongs to a family of nonselective cation channels that function in a variety of processes, including temperature sensation and vasoregulation. The thermosensitive members of this family are expressed in subsets of sensory neurons that terminate in the skin, and are activated at distinct physiological temperatures. This channel is activated at temperatures between 22 and 40 degrees C. This gene lies in close proximity to another family member gene on chromosome 17, and the two encoded proteins are thought to associate with each other to form heteromeric channels. Multiple transcript variants encoding different isoforms have been found for this gene.
transient receptor potential cation channel, subfamily V, member 3
, transient receptor potential cation channel subfamily V member 3-like
, transient receptor potential cation channel subfamily V member 3
, vanilloid receptor-like 3
, vanilloid receptor-related osmotically activated channel protein
, TRP ion channel TRPV3
, heat sensitive channel TRPV3