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WB analysis of cell lysate either with overexpressed recombinant HTT fragment (lane 1) or without (lane 2) using GTX31097 Huntingtin (neoepitope 513) antibody [3-19]. Dilution : 1:500 Loading: 20 microg
WB analysis of cell lysate either with overexpressed recombinant HTT fragment (lane 1) or without (lane 2) using GTX31097 Huntingtin (neoepitope 513) antibody [3-19]. Dilution : 1:500 Loading: 20 microg
WB analysis of cell lysate either with overexpressed recombinant HTT fragment (lane 1) or without (lane 2) using GTX31097 Huntingtin (neoepitope 513) antibody [3-19]. Dilution : 1:500 Loading: 20 microg

Huntingtin (neoepitope 513) antibody [3-19]

Research Use Only
GTX31097
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse
TargetHTT
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Overview

  • Supplier
    GeneTex
  • Product Name
    Huntingtin (neoepitope 513) antibody [3-19]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody recognizes the 513 cleaved fragment without detecting the full-length form.
  • Application Supplier Note
    WB: 1:500. ICC/IF: 2 microg/ml. ELISA: 1:100. IHC: 1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    3-19
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Formulation
    Liquid
  • Gene ID3064
  • Target name
    HTT
  • Target description
    huntingtin
  • Target synonyms
    HD; huntingtin; huntington disease protein; IT15; LOMARS
  • Host
    Mouse
  • Isotype
    IgG
  • Protein IDP42858
  • Protein Name
    Huntingtin
  • Scientific Description
    Huntingtin is a disease gene linked to Huntingtons disease, a neurodegenerative disorder characterized by loss of striatal neurons. This is thought to be caused by an expanded, unstable trinucleotide repeat in the huntingtin gene, which translates as a polyglutamine repeat in the protein product. A fairly broad range of trinucleotide repeats (9-35) has been identified in normal controls, and repeat numbers in excess of 40 have been described as pathological. The huntingtin locus is large, spanning 180 kb and consisting of 67 exons. The huntingtin gene is widely expressed and is required for normal development. It is expressed as 2 alternatively polyadenylated forms displaying different relative abundance in various fetal and adult tissues. The larger transcript is approximately 13.7 kb and is expressed predominantly in adult and fetal brain whereas the smaller transcript of approximately 10.3 kb is more widely expressed. The genetic defect leading to Huntingtons disease may not necessarily eliminate transcription, but may confer a new property on the mRNA or alter the function of the protein. One candidate is the huntingtin-associated protein-1, highly expressed in brain, which has increased affinity for huntingtin protein with expanded polyglutamine repeats. This gene contains an upstream open reading frame in the 5 UTR that inhibits expression of the huntingtin gene product through translational repression. [provided by RefSeq, Jul 2016]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203