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CACNA1C encodes an alpha-1 subunit of a voltage-dependent calcium channel. Zusätzlich bieten wir Ihnen Calcium Channel, Voltage-Dependent, L Type, alpha 1C Subunit Proteine (9) und Calcium Channel, Voltage-Dependent, L Type, alpha 1C Subunit Kits (5) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 162 products:
Hamster Monoclonal CACNA1C Primary Antibody für ICC, IF - ABIN361759
Krey, Moussay, Thiel, Ruemenapf: Role of the low-density lipoprotein receptor in entry of bovine viral diarrhea virus. in Journal of virology 2006
Zeige alle 3 Referenzen für ABIN361759
Human Polyclonal CACNA1C Primary Antibody für EIA, IP - ABIN1105621
Lemke, Welling, Christel, Blaich, Bernhard, Lenhardt, Hofmann, Moosmang: Unchanged beta-adrenergic stimulation of cardiac L-type calcium channels in Ca v 1.2 phosphorylation site S1928A mutant mice. in The Journal of biological chemistry 2008
Human Polyclonal CACNA1C Primary Antibody für EIA, WB - ABIN375180
Saud, Minobe, Wang, Han, Horiuchi, Hao, Kameyama: Calpastatin binds to a calmodulin-binding site of cardiac Cav1.2 Ca2+ channels. in Biochemical and biophysical research communications 2007
Human Polyclonal CACNA1C Primary Antibody für IHC, WB - ABIN1742110
Kreuzberg, Theissen, Schicha, Schröder, Mehlhorn, de Vivie, Bokník, Neumann, Grohé, Herzig: Single-channel activity and expression of atrial L-type Ca(2+) channels in patients with latent hyperthyroidism. in American journal of physiology. Heart and circulatory physiology 2000
Competitive and non-competitive regulation of calcium-dependent inactivation in CaV1.2 L-type Ca2 (zeige CA2 Antikörper)+ channels by calmodulin (zeige Calm2 Antikörper) and Ca2 (zeige CA2 Antikörper)+-binding protein 1.
a direct physical interaction between the N terminus (NT) and C terminus (CT) of the main subunit of the L-type Ca(2 (zeige CA2 Antikörper)+) channel CaV1.2, alpha1C, is reported.
These results reveal a new dimension of regulation of Ca(V)1.2 channels through phosphorylation of the Hook domains of their beta subunits.
These findings suggest that N-glycosylation contributes to the surface expression and voltage-dependent gating of Cav1.2.
Data show that cardiac L-type calcium (CaV1.2) channels form clusters that undergo dynamic, reciprocal, allosteric interactions.
these findings provide evidence for a new role of Homer1 (zeige HOMER1 Antikörper) supporting the regulation of Cav1.2 channels by STIM1 (zeige STIM1 Antikörper).
structural flexibility of CaV1.2 and CaV2.2 (zeige CACNA1B Antikörper) I-II proximal linker
These results suggest a complex antagonistic interplay between G(q)-activated PKC and Gbetagamma in regulation of L-VDCC, in which multiple cytosolic segments of alpha(1C) are involved.
There were substantial transmural gradients in Cav1.2, KChIP2 (zeige KCNIP2 Antikörper), ERG (zeige KCNH2 Antikörper), KvLQT1 (zeige KCNQ1 Antikörper), Kir2.1 (zeige KCNJ2 Antikörper), NCX1 (zeige SLC8A1 Antikörper), SERCA2a (zeige ATP2A2 Antikörper) and RyR2 (zeige RYR2 Antikörper) at the mRNA and, in some cases, protein level-in every case the mRNA or protein was more abundant in the epicardium than the endocardium.
Ca v1.2 binding site for PP2A and PP2B
Swapping the I-II intracellular linker between L-type CaV1.2 and R-type CaV2.3 (zeige CACNA1E Antikörper) high-voltage gated calcium channels exchanges activation attributes.
Copy number increase of CACNA1C are associated with esophageal squamous cell carcinoma.
CACNA1C modulates the cellular rhythm amplitude response to lithium, providing a specific link between LTCCs and circadian rhythms in the context of Bipolar disorder and lithium
Findings indicate that CACNA1C-related differences in amygdala structure and function are present by adolescence.
The associations of CACNA1C rs10774035 with outcome in schizophrenia-spectrum and non-association with outcome in bipolar disorders
Single nucleotide polymorphism in an intron of the CACNA1C gene conveyed an increased risk for developing Bipolar disorder.
CACNA1C risk variant affects facial emotion recognition in healthy individuals.
This integrative genomic study confirmed the role of RUNX2 (zeige RUNX2 Antikörper) as a potential driver of AS and identified a new AS susceptibility gene, CACNA1C, belonging to the calcium signaling pathway.
Study suggests initial support for a link between bipolar disorder risk SNPs rs472913 (1p32.1) and rs1006737 (CACNA1C) and brain arousal regulation
we investigated the association of CACNA1C and ANK3 (zeige ANK3 Antikörper) with SZ using meta-analytic techniques.
Meta-analysis associated CACNA1C single nucleotide polymorphisms with schizophrenia family samples
Results provide evidence that decreased Cacna1c expression has a protective role in the modulation of age-related cognitive declines, and support an interaction between Cacna1c, sex and memory impairment
Both the extracellular PFXYD motif and the transmembrane domain of PLM (zeige FXYD1 Antikörper) but not the cytoplasmic tail were necessary for regulation of peak L-type Ca(2 (zeige CA2 Antikörper)+) current amplitude.
Treatment of MSC (zeige MSC Antikörper) with BMP4 (zeige BMP4 Antikörper) caused a significant increase in expression of Cav1.2, a delay in expression of Cav1.1 (zeige CACNA1S Antikörper), and a reduction in the duration of calcium transients when extracellular calcium was removed
data suggest that miR (zeige MLXIP Antikörper)-103 inhibits osteoblast proliferation mainly through suppression of Cav1.2 expression under simulated microgravity condition
The down-regulation of Cav1.2 expression and the inhibition of LTCCs caused by mechanical unloading in osteoblasts are partially due to miR (zeige MLXIP Antikörper)-103 up-regulation.
Ammonium-induced deregulation of astroglial Ca(2 (zeige CA2 Antikörper)+) signalling, is, in part, associated with upregulation of Cav1.2 L-type calcium channels
Methamphetamine alters DNA methylation (zeige HELLS Antikörper), expression, and protein abundance of CACNA1C.
demonstrate for the first time that both Cav1.2 and Cav1.3 (zeige CACNA1D Antikörper) are necessary for neuronal survival but are differentially required for the biophysical properties of neurons
Our findings reveal that the intra-SR protein (zeige RNPS1 Antikörper) Casq2 (zeige CASQ2 Antikörper) is largely responsible for the phenomenon of SR Ca(2 (zeige CA2 Antikörper)+) release refractoriness in murine ventricular myocytes.
results suggest the involvement of Cacna1c (Cav1.2) in fast electroencephalogram oscillations and REM (zeige REM1 Antikörper) sleep regulatory processes
These results suggest that structural rearrangements of CaV1.2 generated through the binding of BayK8644 or FPL64176, by altering the channel activity, could affect depolarization-evoked catecholamine secretion prior to cation transport.
CaV3.1 (zeige CACNA1G Antikörper) structural analysis and comparison to CaV1.2 channel
These results suggest that PKA and phosphatase(s) attached on or near the Ca(V)1.2 channel regulate the basal channel activity, presumably through modulation of the dynamic CaM (zeige CALM Antikörper) interaction with the channel.
CaM (zeige CALM Antikörper) may tether to the channel with its single lobe, leading to multiple CaM (zeige CALM Antikörper) molecule binding to increase the grade of Ca(2 (zeige CA2 Antikörper)+)-dependent regulation of Cav1.2
This gene encodes an alpha-1 subunit of a voltage-dependent calcium channel. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. The alpha-1 subunit consists of 24 transmembrane segments and forms the pore through which ions pass into the cell. The calcium channel consists of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. There are multiple isoforms of each of these proteins, either encoded by different genes or the result of alternative splicing of transcripts. The protein encoded by this gene binds to and is inhibited by dihydropyridine. Alternative splicing results in many transcript variants encoding different proteins. Some of the predicted proteins may not produce functional ion channel subunits.
, island beat
, voltage-dependent L-type calcium channel subunit alpha-1C
, L-type Ca channel alpha 1 subunit
, L-type calcium channel CaV1.2
, atrium L-type calcium channel
, calcium channel, voltage-dependent, L type, alpha 1C subunit
, voltage-dependent L-type calcium channel subunit alpha-1C-like
, calcium channel voltage-dependent L type Cav1.2, alpha 1c subunit
, CaCB receptor
, smooth muscle calcium channel blocker
, DHPR, alpha-1 subunit
, calcium channel, L type, alpha-1 polypeptide, isoform 1, cardiac muscle
, calcium channel, cardic dihydropyridine-sensitive, alpha-1 subunit
, voltage-gated L-type calcium channel Cav1.2 alpha 1 subunit, splice variant 10*
, L-type Cav1.2
, brain class C
, calcium channel voltage-dependent alpha1c subunit
, neuronal voltage-gated calcium channel alpha 1C subunit
, skeletal muscle-specific calcium channel
, voltage-gated calcium channel subunit alpha Cav1.2
, L-type calcium channel alpha-1 subunit
, calcium channel, voltage-dependent, alpha 1C subunit
, voltage-gated calcium channel alpha 1C subunit
, L-type voltage-gated calcium channel alpha1C subunit ChCaChA1C
, L-type voltage-dependent calcium channel alpha-1 subunit
, cardiac L-type calcium channel
, Voltage-dependent L-type calcium channel subunit alpha-1C