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WB analysis of human brain lysate using GTX89544 Neuroserpin antibody, C-term. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human brain lysate using GTX89544 Neuroserpin antibody, C-term. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human brain lysate using GTX89544 Neuroserpin antibody, C-term. Dilution : 1microg/ml Loading : 35microg protein in RIPA buffer

Neuroserpin antibody, C-term

GTX89544
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetSERPINI1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Neuroserpin antibody, C-term
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID5274
  • Target name
    SERPINI1
  • Target description
    serpin family I member 1
  • Target synonyms
    HNS-S1, HNS-S2, PI12, neuroserpin, neuroserpin, PI-12, peptidase inhibitor 12, serine (or cysteine) proteinase inhibitor, clade I (neuroserpin), member 1, serpin I1, serpin peptidase inhibitor clade I member 1, serpin peptidase inhibitor, clade I (neuroserpin), member 1
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ99574
  • Protein Name
    Neuroserpin
  • Scientific Description
    This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203