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WB analysis of HeLa lysate using GTX88225 SPARTIN antibody, Internal. Dilution : 2microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of HeLa lysate using GTX88225 SPARTIN antibody, Internal. Dilution : 2microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of HeLa lysate using GTX88225 SPARTIN antibody, Internal. Dilution : 2microg/ml Loading : 35microg protein in RIPA buffer

SPARTIN antibody, Internal

GTX88225
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman
TargetSPART
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Overview

  • Supplier
    GeneTex
  • Product Name
    SPARTIN antibody, Internal - KO/KD Validated
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID23111
  • Target name
    SPART
  • Target description
    spartin
  • Target synonyms
    spartin; spastic paraplegia 20 (Troyer syndrome); SPG20; TAHCCP1; trans-activated by hepatitis C virus core protein 1
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ8N0X7
  • Protein Name
    Spartin
  • Scientific Description
    This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome). [provided by RefSeq, Nov 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203