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IHC-P analysis of human brain tissue using GTX31480 SHANK3 antibody. Working concentration : 2.5 microg/ml
IHC-P analysis of human brain tissue using GTX31480 SHANK3 antibody. Working concentration : 2.5 microg/ml
IHC-P analysis of human brain tissue using GTX31480 SHANK3 antibody. Working concentration : 2.5 microg/ml

SHANK3 antibody

GTX31480
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetSHANK3
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Overview

  • Supplier
    GeneTex
  • Product Name
    SHANK3 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 microg/mL. IHC-P: 2.5 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID85358
  • Target name
    SHANK3
  • Target description
    SH3 and multiple ankyrin repeat domains 3
  • Target synonyms
    DEL22q13.3; proline rich synapse associated protein 2; PROSAP2; PSAP2; SCZD15; SH3 and multiple ankyrin repeat domains protein 3; shank postsynaptic density protein; shank3 postsynaptic density protein; SPANK-2
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9BYB0
  • Protein Name
    SH3 and multiple ankyrin repeat domains protein 3
  • Scientific Description
    This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203