KCND3 Produkte
(Potassium Voltage-Gated Channel, Shal-Related Subfamily, Member 3 (KCND3))
Kategorien
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Ausgewählte KCND3 Kategorien
KCND3 Antikörper
High quality antibodies with extensive validation data.
KCND3 Proteine
Proteins for various applications incl. WB, ELISA, IF etc.
Empfohlene KCND3 Antikörper
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- (2)
- (1)
Empfohlene KCND3 ELISA Kits
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Empfohlene KCND3 Proteine
Neueste Publikationen zu unseren KCND3 Produkten
: "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).
Synonyme und alternative Namen zu KCND3
potassium voltage-gated channel subfamily D member 3 (KCND3), potassium voltage-gated channel subfamily D member 3 (kcnd3), potassium voltage-gated channel, Shal-related subfamily, member 3 (kcnd3), potassium channel, voltage gated Shal related subfamily D, member 3 (kcnd3), potassium voltage-gated channel, Shal-related family, member 3 (Kcnd3), potassium voltage-gated channel subfamily D member 3 (Kcnd3), potassium channel, voltage gated Shal related subfamily D, member 3 L homeolog (kcnd3.L), AW045978, K(v)4.3, KCND3, kcnd3-A, KCND3L, KCND3S, Kncd3, KSHIVB, kv4.3, Kv4.3, KV4.3, wu:fi06g01, xKv4.3, zgc:55306Bezeichner auf Proteinebene für KCND3
- potassium voltage-gated channel, Shal-related subfamily, member 3
- potassium voltage-gated channel subfamily D member 3-like
- potassium voltage-gated channel subfamily D member 3
- potassium voltage-gated channel, Shal-related family, member 3
- zShal3
- potassium channel Kv4.3
- potassium voltage-gated channel Shal-related subfamily member 3
- potassium channel Kv4.3L
- potassium channel Kv4.3M
- voltage-gated potassium channel subunit Kv4.3
- potassium ionic channel Kv4.3
- sha1-related potassium channel Kv4.3
- voltage-gated K+ channel
- potassium voltage gated channel, Shal-related family, member 3