KCNT1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-52085
Catalog Number: E-AB-52085
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse, rat
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Background:
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.
Research Area: Neuroscience
Synonyms:
bA100C15.2, EIEE14, ENFL5, KCa4.1, KCNT1, KCNT1, Potassium channel subfamily T member 1, Potassium channel, sodium activated subfamily T, member 1, Potassium channel, subfamily T, member 1 , Sequence like a calcium-activated K+ channel, SLACK , Slo2.2
Immunogen: Synthetic peptide of human KCNT1
Swissprot: Q5JUK3
Gene Accession: NP065873
Purification Method: Antigen affinity purification
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Concentration: 0.9 mg/mL
Dilution: IHC 1:30-1:150, ELISA 1:5000-1:10000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Neuroscience
Synonyms:
bA100C15.2, EIEE14, ENFL5, KCa4.1, KCNT1, KCNT1, Potassium channel subfamily T member 1, Potassium channel, sodium activated subfamily T, member 1, Potassium channel, subfamily T, member 1 , Sequence like a calcium-activated K+ channel, SLACK , Slo2.2
Immunogen: Synthetic peptide of human KCNT1
Swissprot: Q5JUK3
Gene Accession: NP065873
Purification Method: Antigen affinity purification
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Concentration: 0.9 mg/mL
Dilution: IHC 1:30-1:150, ELISA 1:5000-1:10000
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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