FANCC (1-275) Rabbit Polyclonal Antibody

CAT#: AP23096PU-N

FANCC (1-275) rabbit polyclonal antibody, Aff - Purified

Product Images

Western Blot Image: Sample (30 ug of whole cell lysate). A: H1299. 7.5% SDS PAGE. FANCC antibody diluted at 1:1000

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  Western Blot Image: Sample (30 ug of whole cell lysate). A: NIH-3T3. 7.5% SDS PAGE. FANCC antibody. FANCC antibody diluted at 1:1000.

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  Human Breast: Formalin-Fixed, Paraffin-Embedded (FFPE)

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  Human Thymus: Formalin-Fixed, Paraffin-Embedded (FFPE)

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  Immunofluorescence analysis of paraformaldehyde-fixed HeLa, using FANCC antibody at 1:200 dilution.

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  Immunofluorescence analysis of paraformaldehyde-fixed HeLa, merged with DNA probe, using FANCC antibody at 1:200 dilution.

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Specifications

Product Data

• Applications: IF, IHC, WB
• Recommended Dilution: Immunocytochemistry.
  Immunofluorescence: 1/100 - 1/200.
  Immunohistochemistry on Paraffin Sections: 10 µg/ml.
  Western Blot: 1/500 - 1/3000.
• Reactivities: Human, Mouse
• Host: Rabbit
• Clonality: Polyclonal
• Immunogen: Recombinant Human protein fragment containing a sequence corresponding to a region within amino acids 1 and 275 of FANCC
• Specificity: This antibody detects FANCC at aa 1-275.
• Formulation: 0.1 M Tris-glycine, pH 7, 10% Glycerol, 0.01% Thimerosal
  State: Aff - Purified
  State: Liquid Ig fraction
• Concentration: lot specific
• Purification: Immunoaffinity Chromatography
• Storage: Store (in aliquots) at -20 °C. Dilute only prior to immediate use. Avoid repeated freezing and thawing.
• Stability: Shelf life: one year from despatch.
• Gene Name: Homo sapiens Fanconi anemia complementation group C (FANCC), transcript variant 1
• Database Link:
  Entrez Gene 14088 MouseEntrez Gene 2176 Human
• Background: 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.
• Synonyms: Fanconi anemia group C protein, FAC, FACC

Reference Data

• Protein Families: Druggable Genome