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WB analysis of colchicine-treated HepG2 (A), UV-treated HeLa (B), colchicine-treated Raw264.7 (C) whole cell lysates using GTX56029 COL4A3 antibody.
WB analysis of colchicine-treated HepG2 (A), UV-treated HeLa (B), colchicine-treated Raw264.7 (C) whole cell lysates using GTX56029 COL4A3 antibody.
WB analysis of colchicine-treated HepG2 (A), UV-treated HeLa (B), colchicine-treated Raw264.7 (C) whole cell lysates using GTX56029 COL4A3 antibody.

COL4A3 antibody

GTX56029
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse
TargetCOL4A3
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Overview

  • Supplier
    GeneTex
  • Product Name
    COL4A3 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID1285
  • Target name
    COL4A3
  • Target description
    collagen type IV alpha 3 chain
  • Target synonyms
    ATS2; ATS3; collagen alpha-3(IV) chain; collagen IV, alpha-3 polypeptide; collagen, type IV, alpha 3 (Goodpasture antigen); tumstatin
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ01955
  • Protein Name
    Collagen alpha-3(IV) chain
  • Scientific Description
    Type IV collagen, the major structural component of basement membranes, is a multimeric protein composed of 3 alpha subunits. These subunits are encoded by 6 different genes, alpha 1 through alpha 6, each of which can form a triple helix structure with 2 other subunits to form type IV collagen. This gene encodes alpha 3. In the Goodpasture syndrome, autoantibodies bind to the collagen molecules in the basement membranes of alveoli and glomeruli. The epitopes that elicit these autoantibodies are localized largely to the non-collagenous C-terminal domain of the protein. A specific kinase phosphorylates amino acids in this same C-terminal region and the expression of this kinase is upregulated during pathogenesis. This gene is also linked to an autosomal recessive form of Alport syndrome. The mutations contributing to this syndrome are also located within the exons that encode this C-terminal region. Like the other members of the type IV collagen gene family, this gene is organized in a head-to-head conformation with another type IV collagen gene so that each gene pair shares a common promoter. [provided by RefSeq, Jun 2010]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203