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WB analysis of mouse thymus tissue lysate using GTX64576 FANCL antibody. The signal was developed with ECL plus-Enhanced. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of mouse thymus tissue lysate using GTX64576 FANCL antibody. The signal was developed with ECL plus-Enhanced. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of mouse thymus tissue lysate using GTX64576 FANCL antibody. The signal was developed with ECL plus-Enhanced. Dilution : 1:1000 Loading : 25microg per lane

FANCL antibody

GTX64576
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetFANCL
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Overview

  • Supplier
    GeneTex
  • Product Name
    FANCL antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:200 - 1:2000. IHC-P: 1:20 - 1:200. *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 ID55120
  • Target name
    FANCL
  • Target description
    FA complementation group L
  • Target synonyms
    E3 ubiquitin-protein ligase FANCL; FAAP43; Fanconi anemia complementation group L; fanconi anemia group L protein; fanconi anemia-associated polypeptide of 43 kDa; PHD finger protein 9; PHF9; POG; RING-type E3 ubiquitin transferase FANCL
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NW38
  • Protein Name
    E3 ubiquitin-protein ligase FANCL
  • Scientific Description
    This gene encodes a ubiquitin ligase that is a member of the Fanconi anemia complementation group (FANC). Members of this group are related by their assembly into a common nuclear protein complex rather than by sequence similarity. This gene encodes the protein for complementation group L that mediates monoubiquitination of FANCD2 as well as FANCI. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2018]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203