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The protein encoded by TRPC6 forms a receptor-activated calcium channel in the cell membrane. De plus, nous expédions Transient Receptor Potential Cation Channel, Subfamily C, Member 6 Protéines (8) et Transient Receptor Potential Cation Channel, Subfamily C, Member 6 Kits (5) et beaucoup plus de produits pour cette protéine.
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Human Polyclonal TRPC6 Primary Antibody pour IP, ELISA - ABIN314245
Foller, Kasinathan, Koka, Lang, Shumilina, Birnbaumer, Lang, Huber: TRPC6 contributes to the Ca(2+) leak of human erythrocytes. dans Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2008
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Mouse (Murine) Polyclonal TRPC6 Primary Antibody pour FACS, ELISA - ABIN269792
Winn, Conlon, Lynn, Farrington, Creazzo, Hawkins, Daskalakis, Kwan, Ebersviller, Burchette, Pericak-Vance, Howell, Vance, Rosenberg: A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. dans Science (New York, N.Y.) 2005
These findings suggest that lysoPC induces CaM (Montrer KRIT1 Anticorps) phosphorylation at Tyr (Montrer TYR Anticorps)(99) by a Src (Montrer SRC Anticorps) family kinase and that phosphorylated CaM (Montrer KRIT1 Anticorps) activates PI3K to produce PIP3, which promotes TRPC6 translocation to the cell membrane.
analysis of a TRPC6-TRPC5 (Montrer TRPC5 Anticorps) channel cascade that restricts endothelial cell movement
potential implications of transient receptor potential (TRP) channels in the pathogenesis of intestinal fibrosis, since they are known to act as cellular stress sensors/transducers affecting intracellular Ca(2 (Montrer CA2 Anticorps)+) homeostasis/dynamics, and are involved in a broad spectrum of cell pathophysiology including inflammation and tissue remodeling.
Studies provide evidence that the TRPC6-mediated signaling pathway in kidney cells is under control of reactive oxygen species under both physiological and pathological conditions. [review]
SARAF (Montrer TMEM66 Anticorps) modulates TRPC1 (Montrer TRPC1 Anticorps), but not TRPC6, channel function in a STIM1 (Montrer STIM1 Anticorps)-independent manner
Functional interaction of upregulated CaSR (Montrer CASR Anticorps) and upregulated TRPC6 in pulmonary artery smooth muscle cells from idiopathic pulmonary arterial hypertension patients may play an important role in the development and progression of sustained pulmonary vasoconstriction and pulmonary vascular remodeling.
Our comprehensive analysis of human disease-causing TRPC6 mutations reveals loss of TRPC6 function as an additional concept of hereditary focal segmental glomerulosclerosis and provides molecular insights into the mechanism responsible for the loss-of-function phenotype of TRPC6 G757D in humans
study demonstrated that the various mechanisms regulating MDR in HCC (Montrer FAM126A Anticorps) cells are calcium dependent through the TRPC6/calcium/STAT3 (Montrer STAT3 Anticorps) pathway. We propose that targeting TRPC6 in HCC (Montrer FAM126A Anticorps) may be a novel antineoplastic strategy, especially combined with chemotherapy
n response to stretching (20%), ATP was released only from the foremost cells at the wound edge; it then diffused to the cells behind the wound edge and activated the P2Y (Montrer P2RY1 Anticorps) receptors, which caused propagating Ca(2 (Montrer CA2 Anticorps)+) waves via TRPC6
Data suggest that targeted manipulation of protein kinase C (Montrer PKC Anticorps) isoforms PKCalpha (Montrer PKCa Anticorps), PKCbeta, and PKCeta might be beneficial in certain proteinuric kidney diseases with altered transient receptor potential cation channel subfamily C member 6 protein (TRPC6) functions.
Insulin increases the expression of TRPC6 channels in podocytes by activation of the calcineurin-dependent pathway.
This study described the expression and functional relevance of TRPC6 in the pathophysiology of HK-2 (Montrer HK2 Anticorps) cell following ischemia reperfusion.
In the present study, we have explored the hypothesis that TRPC3 (Montrer TRPC3 Anticorps) and TRPC6 channels expressed in VSMCs may have a differential contribution to the regulation of vascular tone, which could be relevant for the changes in vascular reactivity associated with essential hypertension
This study demonstrated that Transient Receptor Potential Canonical 6 (TRPC6) and Orai2 (Montrer ORAI2 Anticorps) form stromal interaction molecule 2 (STIM2 (Montrer Stim2 Anticorps))-regulated neuronal-store-operated Ca(2 (Montrer CA2 Anticorps)+) influx (nSOC) channel complex in hippocampal synapse and the resulting Ca(2 (Montrer CA2 Anticorps)+) influx is critical for long-term maintenance of mushroom spines in hippocampal neurons.
ASIV may prevent HG-induced podocyte apoptosis via downregulation of TRPC6, which is possibly mediated via the calcineurin/NFAT (Montrer NFATC1 Anticorps) signaling pathway.
the mTORC2 (Montrer CRTC2 Anticorps)/Akt (Montrer AKT1 Anticorps)/NFkappaB pathway-mediated activation of TRPC6 participates in adriamycin-induced podocyte apoptosis.
AngII-injured podocyte had a significant increase in apoptosis, while silencing TRPC6 could decrease the apoptosis induced by AngII.
TRPC3 (Montrer TRPC3 Anticorps) and TRPC6 participate diversely in synaptic reorganization in the mossy fiber pathway in temporal lobe epilepsy.
the transient receptor potential canonical-6 (TRPC6) calcium-permeable channel in the alveolar macrophages also functions to shunt the transmembrane potential generated by proton pumping.
Selectively activating endothelial TRPC6 rescues transendothelial migration
MicroRNA-26a prevents endothelial cell apoptosis by directly targeting TRPC6 in the setting of atherosclerosis.
These findings indicate that the mTORC2 (Montrer CRTC2 Anticorps) signaling pathway regulates TRPC6 in podocytes but that the mTORC1 signaling pathway does not appear to exert an effect on TRPC6.
Data found that the pig adrenal medulla expressed predominantly TRPC1 (Montrer TRPC1 Anticorps), TRPC5 (Montrer TRPC5 Anticorps), and TRPC6 transcripts. The expression level of these TRPCs was significantly elevated in the adrenal medulla from pigs with metabolic syndrome.
The protein encoded by this gene forms a receptor-activated calcium channel in the cell membrane. The channel is activated by diacylglycerol and is thought to be under the control of a phosphatidylinositol second messenger system. Activation of this channel occurs independently of protein kinase C and is not triggered by low levels of intracellular calcium. Defects in this gene are a cause of focal segmental glomerulosclerosis 2 (FSGS2).
transient receptor potential cation channel, subfamily C, member 6
, short transient receptor potential channel 6-like
, short transient receptor potential channel 6
, transient receptor protein 6
, calcium entry channel
, transient receptor potential channel subfamily C member 6