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FANCG polyclonal antibody

  • Catalog # : PAB6485
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of FANCG.
  • Immunogen:
  • A synthetic peptide corresponding to human FANCG.
  • Sequence:
  • LEEFRTSLPKSCDL
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 68.5
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:32000)
    Western Blot (0.5-1 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • FANCG polyclonal antibody (Cat # PAB6485) staining (0.5 ug/mL) of HeLa cell lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • HEK293 overexpressing FANCG and probed with FANCG polyclonal antibody (Cat # PAB6485) (mock transfection in first lane), tested by Origene.
  • ELISA
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Western Blot (Transfected lysate)
  • Western Blot (Transfected lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 2189
  • Gene Name:
  • FANCG
  • Gene Alias:
  • FAG,XRCC9
  • Gene Description:
  • Fanconi anemia, complementation group G
  • Gene Summary:
  • The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group G. [provided by RefSeq
  • Other Designations:
  • DNA repair protein XRCC9,OTTHUMP00000021319,X-ray repair complementing defective repair in Chinese hamster cells 9,X-ray repair, complementing defective, in Chinese hamster, 9
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