Bio-Connect

Nav1.8 Antibody: APC

ORB148840
Biorbyt
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Monkey, Mouse, Rat
TargetScn10a
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Overview

  • Supplier
    Biorbyt
  • Product Name
    Nav1.8 antibody
  • Delivery Days Customer
    16
  • Application Supplier Note
    1 microg/ml of SMC-342 was sufficient for detection of Nav1.8 in 10 microg of COS cell lysate transiently expressing Nav1.8 by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Applications Supplier
    WB (1:1000), IHC (1:1000), ICC/IF (1:100) ICC, IF, IHC
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    S134
  • Concentration
    1 mg/ml
  • Conjugate
    APC (Allophycocyanin)
  • Gene ID29571
  • Target name
    Scn10a
  • Target description
    sodium voltage-gated channel alpha subunit 10
  • Target synonyms
    Na(V)1.8; Nav1.8; peripheral nerve sodium channel 3; PN3; sensory neuron sodium channel; sodium channel protein type 10 subunit alpha; sodium channel protein type X subunit alpha; sodium channel type X alpha polypeptide; sodium channel voltage-gated type X alpha polypeptide; sodium channel, voltage-gated, type 10, alpha polypeptide; sodium channel, voltage-gated, type X, alpha subunit; voltage-gated sodium channel subunit alpha Nav1.8
  • Host
    Mouse
  • Isotype
    IgG2a
  • Protein IDQ62968
  • Protein Name
    Sodium channel protein type 10 subunit alpha
  • Scientific Description
    Mouse monoclonal to Nav1 (APC). 8. Nav1. 8 is a voltage-gated sodium channel and plays a critical role in the generation and conduction of action potentials and is thus important for electrical signaling by most excitable cells. Therapeutically, the association of pain insensitivity with the loss of function of a certain sodium channel may have implications. Since Nav1. 8 is not present in cardiac muscle or neurons in the central nervous system, blockers of Nav1. 8 will not have direct action on these cells and thus can have less side effects than current pain medications. By performing more studies, there is a possibility to develop a new generation of drugs that can reduce the pain intensity in animals..
  • Reactivity
    Human, Monkey, Mouse, Rat
  • Storage Instruction
    See Manual
  • UNSPSC
    12352203