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WB analysis of rat brain tissue lysate using GTX17027 AIPL1 antibody. Working concentration : (A) 1 and (B) 2 microg/ml
WB analysis of rat brain tissue lysate using GTX17027 AIPL1 antibody. Working concentration : (A) 1 and (B) 2 microg/ml
WB analysis of rat brain tissue lysate using GTX17027 AIPL1 antibody. Working concentration : (A) 1 and (B) 2 microg/ml

AIPL1 antibody

Research Use Only
GTX17027
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetAIPL1
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Overview

  • Supplier
    GeneTex
  • Product Name
    AIPL1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 - 2 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
  • Formulation
    Liquid
  • Gene ID23746
  • Target name
    AIPL1
  • Target description
    aryl hydrocarbon receptor interacting protein like 1
  • Target synonyms
    AIPL2; aryl-hydrocarbon-interacting protein-like 1; LCA4
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NZN9
  • Protein Name
    Aryl-hydrocarbon-interacting protein-like 1
  • Scientific Description
    Leber congenital amaurosis (LCA) accounts for at least 5% of all inherited retinal disease and is the most severe inherited retinopathy with the earliest age of onset. Individuals affected with LCA are diagnosed at birth or in the first few months of life with severely impaired vision or blindness, nystagmus and an abnormal or flat electroretinogram. The photoreceptor/pineal -expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, was mapped within the LCA4 candidate region. The protein contains three tetratricopeptide motifs, consistent with nuclear transport or chaperone activity. AIPL1 mutations may cause approximately 20% of recessive LCA. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203