KCNT1 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES6922
Catalog Number: ELK-ES6922
Reactivity: Human, Mouse, Rat
Applications: WB, IHC-p, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Reactivity: Human, Mouse, Rat
Applications: WB, IHC-p, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
potassium sodium-activated channel subfamily T member 1(KCNT1) Homo sapiens Potassium 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. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012],
Alternative Names:
KCNT1, KIAA1422, Potassium channel subfamily T member 1, KCa4.1
Immunogen: The antiserum was produced against synthesized peptide derived from human KCNT1. AA range:1019-1068
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 140
GeneID: KCNT1
Storage: -20°C/1 year
NOTE: For Research Use Only
potassium sodium-activated channel subfamily T member 1(KCNT1) Homo sapiens Potassium 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. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012],
Alternative Names:
KCNT1, KIAA1422, Potassium channel subfamily T member 1, KCa4.1
Immunogen: The antiserum was produced against synthesized peptide derived from human KCNT1. AA range:1019-1068
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 140
GeneID: KCNT1
Storage: -20°C/1 year
NOTE: For Research Use Only
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