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IHC-P analysis of human brain tissue using GTX87812 KCNT1 antibody. The picture on the right is blocked with the synthesized peptide.
IHC-P analysis of human brain tissue using GTX87812 KCNT1 antibody. The picture on the right is blocked with the synthesized peptide.
IHC-P analysis of human brain tissue using GTX87812 KCNT1 antibody. The picture on the right is blocked with the synthesized peptide.

KCNT1 antibody

GTX87812
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetKCNT1
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Overview

  • Supplier
    GeneTex
  • Product Name
    KCNT1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:50~1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID57582
  • Target name
    KCNT1
  • Target description
    potassium sodium-activated channel subfamily T member 1
  • Target synonyms
    bA100C15.2; DEE14; EIEE14; ENFL5; KCa4.1; 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
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ5JUK3
  • Protein Name
    Potassium channel subfamily T member 1
  • Scientific Description
    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]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203