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WB analysis of various sample lysates using GTX64424 Fibulin 5 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX64424 Fibulin 5 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX64424 Fibulin 5 antibody. Dilution : 1:1000 Loading : 25microg per lane

Fibulin 5 antibody

GTX64424
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman, Mouse
TargetFBLN5
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Overview

  • Supplier
    GeneTex
  • Product Name
    Fibulin 5 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID10516
  • Target name
    FBLN5
  • Target description
    fibulin 5
  • Target synonyms
    ADCL2; ARCL1A; ARMD3; DANCE; developmental arteries and neural crest EGF-like protein; embryonic vascular EGF-like repeat-containing protein; EVEC; FIBL-5; fibulin-5; HNARMD; testis tissue sperm-binding protein Li 75n; UP50; urine p50 protein
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9UBX5
  • Protein Name
    Fibulin-5
  • Scientific Description
    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3). [provided by RefSeq, Jul 2008]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203