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TRPV4 encodes a member of the OSM9-like transient receptor potential channel (OTRPC) subfamily in the transient receptor potential (TRP) superfamily of ion channels. Zusätzlich bieten wir Ihnen TRPV4 Proteine (6) und TRPV4 Kits (2) und viele weitere Produktgruppen zu diesem Protein an.
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Mouse (Murine) Polyclonal TRPV4 Primary Antibody für IHC, WB - ABIN351282
Arniges, Fernuandez-Fernuandez, Albrecht, Schaefer, Valverde: Human TRPV4 channel splice variants revealed a key role of ankyrin domains in multimerization and trafficking. in The Journal of biological chemistry 2006
Zeige alle 6 Referenzen für ABIN351282
Chicken Polyclonal TRPV4 Primary Antibody für IHC, WB - ABIN2776284
Sampat, Dermksian, Oungoulian, Winchester, Bulinski, Ateshian, Hung: Applied osmotic loading for promoting development of engineered cartilage. in Journal of biomechanics 2013
TRPP2 and TRPV4 are mechanosensitive channels in the endocardium.Oscillatory flow modulates mechanosensitive klf2a expression through trpv4 and trpp2 during heart valve development.
TRPP2 utilizes TRPV4 to form a mechano- and thermosensitive molecular sensor in the cilium.
Age-dependence of heat-activated seizure susceptibility mimicks the mRNA expression of TRPV4 and glutamate (zeige GRIN2A Antikörper) receptors.
TRPV4 present in all sensory organs of adult zebrafish.
Study reports cloning of a zebrafish trpv4 cDNA and assaying its expression during embryogenesis; trpv4 is expressed as maternal mRNA in 4-cell embryos and later zygotic expression is first observed in the forming notochord at the one somite stage.
OS-9 (zeige OS9 Antikörper) regulates the secretory transport of TRPV4 and appears to protect TRPV4 subunits from the precocious ubiquitination and ER-associated degradation.
the activation of myenteric TRPV4 and the subsequent production of NO by these neurons have the potential to become an important target for the pharmacological treatment of GI disorders with predominant hypermotility symptoms.
these data strongly suggest endogenous TRPV4 channels as a mechanosensor, mediating cyclic stretch-induced realignment of hESC-CMs (zeige Cd2ap Antikörper).
Identify TRPV4 as novel regulator of neutrophil activation and suggest contributions of both parenchymal and neutrophilic TRPV4 in the pathophysiology of acute lung injury.
TRPV4 regulates dynamics of trailing adhesions.
A mutation in TRPV4 results in altered chondrocyte calcium signaling in severe metatropic dysplasia.
Calcium sensitive TRPV4 translocation is associated with the regulation of endothelial response to mechanical stimulation.
The inflammatory cytokine TNF-a (zeige TNF Antikörper) can modulate the activity of the mechanosensitive ion channels TRPA1 (zeige TRPA1 Antikörper) and TRPV4 in odontoblasts via the p38 MAPK (zeige MAPK14 Antikörper) pathway but has differential effects on their expression.
Interaction between the linker, pre-S1, and TRP (zeige TBPL1 Antikörper) domains determines folding, assembly, and trafficking of TRPV1 (zeige TRPV1 Antikörper) and TRPV4 channels.
Neurography revealed a late-onset sensory neuropathy in the father, which was so far not described in TRPV4 neuropathies.
P2Y1 (zeige P2RY1 Antikörper) couples to and activates TRPV4. PKC (zeige PRRT2 Antikörper) inhibitors prevented P2Y1 receptor (zeige P2RY1 Antikörper) activation of TRPV4.
In subcutaneous adipose tissue, a high fat diet elevated TRPV4, exercise, and exercise plus rutin completely reduced TRPV4 to normal level.
TRPV4 regulates neuronal excitability and social behavior through its activation at the physiological temperature in vivo.
TRPV4-mediated nociceptive information from the peripheral tissue excluding the spinal pathway might be involved the formalin behavioral response during phase I. Only TRPV1 (zeige TRPV1 Antikörper) might regulate the formalin behavioral response in peripheral neuron.
TRPV4 channels regulate tumor angiogenesis by selectively inhibiting tumor endothelial cell proliferation.
Our findings demonstrate TRPV4 channels to be critical regulators of tumor angiogenesis and represent a novel target for anti-angiogenic and vascular normalization therapies.
GPCR (zeige GPBAR1 Antikörper)-TRPV4 channel interactions comprise a key signalling pathway for the endothelium-dependent regulation of vascular tone.
The findings suggest that signaling through TRPV4, triggered by changes in extracellular matrix stiffness, cooperates with LPS (zeige TLR4 Antikörper)-induced signals to mediate macrophage phagocytic function and lung injury resolution.
Data suggest that blockage of transient receptor potential (TRP) channels TRPA1 (zeige TRPA1 Antikörper), TRPV4 and possibly TRPM8 (zeige TRPM8 Antikörper) may represent a therapeutic option for patients with colonic discomfort and pain.
This study strongly suggests that DRG TRPV1 (zeige TRPV1 Antikörper) overexpression and pERK (zeige EIF2AK3 Antikörper) signaling, as well as spinal cord TRPV1 (zeige TRPV1 Antikörper) and TRPV4 overexpression, mediate hyperalgesia in a mouse fibromyalgia pain model.
Data indicate a physiologic function of transient receptor potential vanilloid 4 (TRPV4) in the regulation of blood-cerebrospinal fluid barrier (BCSFB) permeability.
Hyposmotic shock-induced TRPV4 channel activation regulates hemichannel-mediated ATP release and Na-K-ATPase (zeige ATP1A1 Antikörper) activity in lens epithelium.
The large amounts of transported calcium and the short signaling ways suggest a potentially important role of TRPV4 in many physiological processes.
TRPV4 is present in articular chondrocytes in swine, and chondrocyte response to hypo-osmotic stress is mediated by this channel, which involves both an extracellular Ca(2 (zeige CA2 Antikörper)+) and intracellular Ca(2 (zeige CA2 Antikörper)+) release.
TRPV4 channels activity in bovine articular chondrocytes are regulated by obesity-associated mediators.
TRPV4 channels mediate cyclic strain-induced endothelial cell reorientation through integrin-to-integrin signaling.
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.
transient receptor potential cation channel subfamily V member 4
, transient receptor potential cation channel, subfamily V, member 4
, transient receptor potential cation channel subfamily V member 4-like
, OSM9-like transient receptor potential channel 4
, osm-9-like TRP channel 4
, osmosensitive transient receptor potential channel 4
, transient receptor potential protein 12
, vanilloid receptor-like channel 2
, vanilloid receptor-related osmotically activated channel
, vanilloid receptor-like protein 2
, vanilloid receptor-related osmotically-activated channel
, transient receptor potential cation channel, subfamily 5, member 4
, vanilloid receptor-related osmotically activated channel (Vroac)
, vanilloid receptor-related osmotically activated channel protein