KCND3 抗体
(Potassium Voltage-Gated Channel, Shal-Related Subfamily, Member 3 (KCND3))
Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog(s). This gene encodes a member of the potassium channel, voltage-gated, shal-related subfamily, members of which form voltage-activated A-type potassium ion channels and are prominent in the repolarization phase of the action potential. This member includes two isoforms with different sizes, which are encoded by alternatively spliced transcript variants of this gene. [provided by RefSeq, Jul 2008].
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Quantity
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WB, IHC, IF, ICC, IP
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Quantity
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Quantity
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Quantity
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Quantity
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Quantity
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Reactivity
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Application
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Validations
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Datasheet
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Latest Publications for our KCND3 抗体
: "Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner." in: Cellular and molecular life sciences : CMLS, Vol. 72, Issue 17, pp. 3387-99, (2015) (PubMed).: "NGF-induced synapse-like structures in contralateral sensory ganglia contribute to chronic mirror-image pain." in: Pain, (2015) (PubMed).
: "Kv4.3-Encoded Fast Transient Outward Current Is Presented in Kv4.2 Knockout Mouse Cardiomyocytes." in: PLoS ONE, Vol. 10, Issue 7, pp. e0133274, (2015) (PubMed).
: "Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function." in: International journal of molecular medicine, Vol. 36, Issue 1, pp. 309-15, (2015) (PubMed).
: "Chronic obstructive sleep apnea causes atrial remodeling in canines: mechanisms and implications." in: Basic research in cardiology, Vol. 109, Issue 5, pp. 427, (2014) (PubMed).
: "Somatodendritic ion channel expression in substantia nigra pars compacta dopaminergic neurons across postnatal development." in: Journal of neuroscience research, Vol. 92, Issue 8, pp. 981-99, (2014) (PubMed).
: "Reduced expression of IA channels is associated with postischemic seizures in hyperglycemic rats." in: Journal of neuroscience research, Vol. 92, Issue 12, pp. 1775-84, (2014) (PubMed).
: "Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19. ..." in: Annals of neurology, Vol. 72, Issue 6, pp. 870-80, (2013) (PubMed).
: "Trafficking of the IKs -complex in MDCK cells: site of subunit assembly and determinants of polarized localization." in: Traffic (Copenhagen, Denmark), Vol. 14, Issue 4, pp. 399-411, (2013) (PubMed).
: "The L450P mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer together." in: Neurogenetics, Vol. 14, Issue 3-4, pp. 257-8, (2013) (PubMed).
Aliases for KCND3 抗体
potassium voltage-gated channel subfamily D member 3 (KCND3) 抗体potassium voltage-gated channel subfamily D member 3 (kcnd3) 抗体
potassium voltage-gated channel, Shal-related subfamily, member 3 (kcnd3) 抗体
potassium channel, voltage gated Shal related subfamily D, member 3 (kcnd3) 抗体
potassium voltage-gated channel, Shal-related family, member 3 (Kcnd3) 抗体
potassium voltage-gated channel subfamily D member 3 (Kcnd3) 抗体
potassium channel, voltage gated Shal related subfamily D, member 3 L homeolog (kcnd3.L) 抗体
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kv4.3 抗体
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