FANCC Antikörper (AA 96-112)
Kurzübersicht für FANCC Antikörper (AA 96-112) (ABIN401268)
Target
Alle FANCC Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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Bindungsspezifität
- AA 96-112
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Spezifität
- This antibody is directed against human FANCC protein.
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Kreuzreaktivität (Details)
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Species reactivity (expected):Chimpanzee (100 %).
Species reactivity (tested):Human. -
Aufreinigung
- Affinity Purified
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Immunogen
- Synthetic peptide corresponding to amino acids 96-112 of Human FANCC
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Isotyp
- IgG
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Applikationshinweise
- ELISA: 1: 20,000 - 1: 80,000. Western blot: 1: 1,000 - 1: 3,000 (Expect a band approximately 63 kDa in size correspondingto FANCC in the appropriate human tissue).
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Konzentration
- 1.45 mg/mL (by UV absorbance at 280 nm)
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Buffer
- 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2, 0.01 % (w/v) Sodium Azide
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Konservierungsmittel
- Sodium azide
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Vorsichtsmaßnahmen
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handhabung
- Avoid repeated freezing and thawing. Should this product contain a precipitate we recommend microcentrifugation before use.
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Lagerung
- 4 °C/-20 °C
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Informationen zur Lagerung
- Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer.
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- FANCC (Fanconi Anemia, Complementation Group C (FANCC))
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Andere Bezeichnung
- FANCC
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Hintergrund
- FANCC (also called Protein FACC or Fanconi Anemia Group C protein) is involved in DNA repair, perhaps specifically with post-replication repair or a cell cycle checkpoint function. FANCC may also be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. FANCC belongs to the multi-subunit Fanconi Anemia (FA) complex composed of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL/PHF9 and FANCM. FANCC is mainly found within the nucleus although some protein is localized in the cytoplasm. This protein is ubiquitously expressed. Defects in FANCC are a cause of Fanconi anemia (FA). FA is a genetically heterogeneous, autosomal recessive disorder characterized by progressive pancytopaenia, a diverse assortment of congenital malformations, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNAdamaging agents, chromosomal instability (increased chromosome breakage), and defective DNA repair.Synonyms: FAC, FACC, Fanconi anemia group C protein
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Gen-ID
- 2176
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NCBI Accession
- NP_000127
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UniProt
- Q00597
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Pathways
- DNA Reparatur
Target
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