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FANCA Antikörper

Der Kaninchen Monoklonal Anti-FANCA-Antikörper wurde für WB validiert. Er ist geeignet, FANCA in Proben von Human zu detektieren.
Produktnummer ABIN7267124

Kurzübersicht für FANCA Antikörper (ABIN7267124)

Target

Alle FANCA Antikörper anzeigen
FANCA (Fanconi Anemia Group A Protein (FANCA))

Reaktivität

  • 48
  • 19
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 61
  • 3
Kaninchen

Klonalität

  • 62
  • 2
Monoklonal

Konjugat

  • 34
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FANCA Antikörper ist unkonjugiert

Applikation

  • 33
  • 26
  • 13
  • 13
  • 12
  • 10
  • 8
  • 6
  • 5
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Verwendungszweck

    FANCA Rabbit mAb

    Kreuzreaktivität

    Human

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human FANCA

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    FANCA (Fanconi Anemia Group A Protein (FANCA))

    Andere Bezeichnung

    FANCA

    Hintergrund

    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 A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008],FA, FA-H, FA1, FAA, FACA, FAH, FANCH,DNA Damage & Repair,Epigenetics & Nuclear Signaling,FANCA

    Molekulargewicht

    163Da

    Gen-ID

    2175

    UniProt

    O15360

    Pathways

    DNA Reparatur
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