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TRPC1 encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Zusätzlich bieten wir Ihnen Transient Receptor Potential Cation Channel, Subfamily C, Member 1 Antikörper (85) und Transient Receptor Potential Cation Channel, Subfamily C, Member 1 Kits (3) und viele weitere Produktgruppen zu diesem Protein an.
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these results suggest that dopaminergic neurotoxins initially decreased Ca(2 (zeige CA2 Proteine)+) entry, which inhibited the binding of NF-kappaB (zeige NFKB1 Proteine) to the TRPC1 promoter, thereby inhibiting TRPC1 expression and resulting in cell death by preventing autophagy.
TRPC1 regulated HIF1alpha (zeige HIF1A Proteine) levels in PTEN-deficient MDA-MB-468 and HCC1569 breast cancer cell lines. This regulation arises from effects on the constitutive translation of HIF1alpha (zeige HIF1A Proteine) under normoxic conditions via an Akt (zeige AKT1 Proteine)-dependent pathway.
Store-operated calcium entry (SOCE), a unique plasma membrane Ca(2 (zeige CA2 Proteine)+) entry mechanism, is activated when ER-[Ca(2 (zeige CA2 Proteine)+)] is decreased. SOCE is mediated via the primary channel, Orai1, as well as others such as TRPC1.
the role of TRPC1 in the development of podocyte injury and disorders of the podocyte cytoskeleton, which may contribute to the development of novel therapeutics for podocyte injury-associated kidney diseases.
TRPC1 is a primary candidate in forming SOCC that stimulates CaSRinduced SOCE and NO production in HUVECs
TRPC1-STIM1 activation modulates transforming growth factor beta-induced epithelial-to-mesenchymal transition and cell migration.
Data show that RNAi-mediated knockdown of KCa3.1 (zeige KCNN4 Proteine) and/or TRPC1 leads to a significant decrease in cell proliferation due to cell cycle arrest in the G1 phase
Data indicate that the inhibition of the Store Operated Calcium Entry (SOCE)-dependent colon cancer cell migration through SK3 (zeige KCNN3 Proteine)/TRPC1/Orai1 channel complex by the alkyl-lipid Ohmline may be a strategy to modulate Anti-EGFR (zeige EGFR Proteine) mAb action in metastatic colorectal cancer (mCRC).
This study provided direct evidence that increasing extracellular Ca(2 (zeige CA2 Proteine)+) enhanced TNF-alpha (zeige TNF Proteine)-induced VCAM-1 (zeige VCAM1 Proteine) activation and monocytes adhesion. Moreover, we identified a novel TRPC1/ERK1/2/NFkappaB (zeige NFKB1 Proteine) signaling pathway mediating VCAM-1 (zeige VCAM1 Proteine) activation and monocyte adhesion in this pathological process.
These observations suggest that mechanical stretch may induce an influx of Ca(2 (zeige CA2 Proteine)+) and up-regulation of IL-13 (zeige IL13 Proteine) and MMP-9 (zeige MMP9 Proteine) expression in 16HBE cells via activation of TRPC1
Endogenous as well as overexpressed xTRPV6 interacts with xTRPC1.
our results suggest that calcium influx through mechanosensitive TRPC1 channels on filopodia activates calpain to control growth cone turning during development.
This study suggested that BDNF (zeige BDNF Proteine)-induced synaptic potentiation involves coordinated presynaptic and postsynaptic responses and identifies TRPC1 as a molecular mediator for postsynaptic Ca2 (zeige CA2 Proteine)+ elevation required for BDNF (zeige BDNF Proteine)-induced synaptic plasticity.
XTRPC1, a Xenopus homolog of mammalian TRPC1, is required for proper growth cone turning responses of Xenopus spinal neurons to netrin-1 (zeige NTN1 Proteine), brain-derived neurotrophic factor (zeige BDNF Proteine) and myelin-associated glycoprotein (zeige MAG Proteine), but not to semaphorin 3A (zeige SEMA3A Proteine).
downregulation of Xenopus TRP-1 (zeige TYRP1 Proteine) (xTRPC1) expression with a specific morpholino oligonucleotide abolished the growth-cone turning and Ca2 (zeige CA2 Proteine)+ elevation induced by a netrin-1 (zeige NTN1 Proteine) gradient
By use of electrophysiology and intracellular Ca2 (zeige CA2 Proteine)+ imaging, this study characterises a Ca2 (zeige CA2 Proteine)+ permeable channel in white adipocytes. The current shows functional characteristics resembling the Ca2 (zeige CA2 Proteine)+ -permeable transient receptor potential channel 1 (TRPC1).
Silencing of beta 1 integrin gene regulates the gene expression of storeoperated Ca2 (zeige CA2 Proteine)+ entry (SOCE)-associated genes (STIM1 (zeige STIM1 Proteine), ORAI1 (zeige TMEM132A Proteine) and TRPC1).
TRPC3-induced Ca2+ entry promotes astrocyte proliferation and migration i.e. astrocyte activity in vitro which is attenuated by the presence of TRPC1. Following brain injury, the absence of TRPC3 results in a significant reduction of astrogliosis and cortical edema in vivo, suggesting that a targeted therapy to reduce TRPC3 channel activity might be beneficial in traumatic brain injury.
Data show that transient receptor potential channel 1 (TRPC1) deficiency caused neuronal apoptosis in basal ganglia.
TRPC1 is indispensable for the enriched environment-induced hippocampal neurogenesis and cognitive enhancement.
Data (including data from studies using knockout mice) suggest that TRPC1 inhibits positive effects of exercise on insulin (zeige INS Proteine) resistance and type II diabetes in a high-fat diet-induced obesity environment.
TRPC1 regulated directly or indirectly the expression of multiple proteins, which may be crucial for the maintenance of memory ability.
we confirmed that the activation of OTX2 (zeige OTX2 Proteine), a determinant of DA neuron development and the expression of which is induced by thyroid hormone (zeige PTH Proteine), is dependent on TRPC1-mediated calcium signaling.
the link between HG-induced changes in TRPC1 expression, enhanced Ca(2 (zeige CA2 Proteine)+) entry, and endothelial dysfunction require further study
These results provide the first in vivo evidence that TRPC1 is essential for angiogenesis in zebrafish.
Demonstrate a novel role of the NO-cGMP-PKG (zeige PRKG1 Proteine) pathway in the inhibition of 11,12-EET-induced smooth muscle hyperpolarization and relaxation via PKG (zeige PRKG1 Proteine)-mediated phosphorylation of TRPC1.
Data found that the pig adrenal medulla expressed predominantly TRPC1, TRPC5 (zeige TRPC5 Proteine), and TRPC6 (zeige TRPC6 Proteine) transcripts. The expression level of these TRPCs was significantly elevated in the adrenal medulla from pigs with metabolic syndrome.
Heteromeric TRPV4 (zeige TRPV4 Proteine)-TRPC1 channels mediate CaSR (zeige CASR Proteine)-induced vasorelaxation through NO production but not IKCa channel activation in rabbit mesenteric arteries.
a novel activation mechanism for TRPC1 SOCs in VSMCs, in which store depletion induces formation of TRPC1-Galphaq-PLCbeta1 complexes that lead to PKC stimulation and channel gating.
The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations. The encoded protein appears to be induced to form channels by a receptor tyrosine kinase-activated phosphatidylinositol second messenger system and also by depletion of intracellular calcium stores. Two transcript variants encoding different isoforms have been found for this gene.
, short transient receptor potential channel 1
, transient receptor potential canonical 1
, transient receptor protein 1
, transient receptor potential protein
, trp-related protein 1
, transient receptor potential channel 1
, store-operated calcium channel
, transient receptor potential channel subfamily C member 1
, transient receptor potential cation channel, subfamily C, member 1
, transient receptor potential cation channel subfamily C member 1
, short transient receptor potential channel 1-like
, calcium influx channel TRPC1A
, putative calcium influx channel TRPC1A