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WB analysis of various samples using GTX53514 COL9A1 antibody. Lane 1: 293 whole cell lysate Lane 2: MCF-7 whole cell lysate Loading : 20 microg per lane Dilution : 1:1000
WB analysis of various samples using GTX53514 COL9A1 antibody. Lane 1: 293 whole cell lysate Lane 2: MCF-7 whole cell lysate Loading : 20 microg per lane Dilution : 1:1000
WB analysis of various samples using GTX53514 COL9A1 antibody. Lane 1: 293 whole cell lysate Lane 2: MCF-7 whole cell lysate Loading : 20 microg per lane Dilution : 1:1000

COL9A1 antibody

GTX53514
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetCOL9A1
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Overview

  • Supplier
    GeneTex
  • Product Name
    COL9A1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:1000. IHC-P: 1:10-1:50. *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
  • Conjugate
    Unconjugated
  • Gene ID1297
  • Target name
    COL9A1
  • Target description
    collagen type IX alpha 1 chain
  • Target synonyms
    alpha-1(IX) collagen chain; cartilage-specific short collagen; collagen alpha-1(IX) chain; collagen IX, alpha-1 polypeptide; collagen, type IX, alpha 1; DJ149L1.1.2; EDM6; MED; STL4
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP20849
  • Protein Name
    Collagen alpha-1(IX) chain
  • Scientific Description
    This gene encodes one of the three alpha chains of type IX collagen, which is a minor (5-20%) collagen component of hyaline cartilage. Type IX collagen is usually found in tissues containing type II collagen, a fibrillar collagen. Studies in knockout mice have shown that synthesis of the alpha 1 chain is essential for assembly of type IX collagen molecules, a heterotrimeric molecule, and that lack of type IX collagen is associated with early onset osteoarthritis. Mutations in this gene are associated with osteoarthritis in humans, with multiple epiphyseal dysplasia, 6, a form of chondrodysplasia, and with Stickler syndrome, a disease characterized by ophthalmic, orofacial, articular, and auditory defects. Two transcript variants that encode different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203