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Factor I antibody [3R/8]

GTX41627
GeneTex
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, Neutralisation/Blocking
Product group Antibodies
ReactivityHuman
TargetCFI
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Overview

  • Supplier
    GeneTex
  • Product Name
    Factor I antibody [3R/8]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody recognizes complement factor I. Clone 3R/8 blocks function of complement factor I.
  • Application Supplier Note
    ELISA: 1/500-1/4,000. Neutralizing/Inhibition: . *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen, Neutralisation/Blocking
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    3R/8
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3426
  • Target name
    CFI
  • Target description
    complement factor I
  • Target synonyms
    AHUS3; ARMD13; C3B/C4B inactivator; C3BINA; C3b-INA; C3b-inactivator; complement component I; complement control protein factor I; complement factor I; complement factor I heavy chain; FI; IF; KAF; Konglutinogen-activating factor; light chain of factor I
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP05156
  • Protein Name
    Complement factor I
  • Scientific Description
    This gene encodes a serine proteinase that is essential for regulating the complement cascade. The encoded preproprotein is cleaved to produce both heavy and light chains, which are linked by disulfide bonds to form a heterodimeric glycoprotein. This heterodimer can cleave and inactivate the complement components C4b and C3b, and it prevents the assembly of the C3 and C5 convertase enzymes. Defects in this gene cause complement factor I deficiency, an autosomal recessive disease associated with a susceptibility to pyogenic infections. Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome, a disease characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Primary glomerulonephritis with immune deposits and age-related macular degeneration are other conditions associated with mutations of this gene. [provided by RefSeq, Dec 2015]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203