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WB analysis of NIH-3T3 (A), HEK293 (B), HepG2 (C) and MCF7 (D) lysates using GTX89049 SOD1 antibody, Internal. Dilution : 0.01microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of NIH-3T3 (A), HEK293 (B), HepG2 (C) and MCF7 (D) lysates using GTX89049 SOD1 antibody, Internal. Dilution : 0.01microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of NIH-3T3 (A), HEK293 (B), HepG2 (C) and MCF7 (D) lysates using GTX89049 SOD1 antibody, Internal. Dilution : 0.01microg/ml Loading : 35microg protein in RIPA buffer

SOD1 antibody, Internal

GTX89049
GeneTex
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman, Mouse
TargetSOD1
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Overview

  • Supplier
    GeneTex
  • Product Name
    SOD1 antibody, Internal
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 0.01-0.03microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID6647
  • Target name
    SOD1
  • Target description
    superoxide dismutase 1
  • Target synonyms
    ALS; ALS1; Cu/Zn superoxide dismutase; epididymis secretory protein Li 44; HEL-S-44; homodimer; hSod1; indophenoloxidase A; IPOA; SOD; SOD, soluble; STAHP; superoxide dismutase [Cu-Zn]; superoxide dismutase 1, soluble; superoxide dismutase, cystolic
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDP00441
  • Protein Name
    Superoxide dismutase [Cu-Zn]
  • Scientific Description
    The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203