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FANCG anticorps (AA 1-25)

Cet anticorps Lapin Polyclonal détecte spécifiquement FANCG dans WB, ELISA et IHC. Il présente une réactivité envers Humain et Souris.
Rockland
N° du produit ABIN129607
N° du produit (Fournisseur): 600-401-671

Aperçu rapide pour FANCG anticorps (AA 1-25) (ABIN129607)

Antigène

Voir toutes FANCG Anticorps
FANCG (Fanconi Anemia Complementation Group G (FANCG))

Reactivité

  • 64
  • 4
  • 2
Humain, Souris

Hôte

  • 59
  • 4
  • 1
Lapin

Clonalité

  • 62
  • 2
Polyclonal

Conjugué

  • 25
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FANCG est non-conjugé

Application

  • 56
  • 26
  • 26
  • 21
  • 13
  • 9
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Épitope

    • 22
    • 15
    • 9
    • 8
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 1-25

    N° du produit (Fournisseur)

    600-401-671

    Fournisseur

    Rockland

    Fonction

    FANCG Antibody

    Réactivité croisée (Details)

    This affinity-purified antibody is directed against human FANCG protein.

    Attributs du produit

    Synonyms: rabbit anti-FANCG antibody, FANC-G, FANC G, Fanconi anemia group G protein, DNA repair protein XRCC9 antibody, Fanconi anaemia complementation group G antibody, Protein FACG antibody

    Purification

    The product was affinity purified from monospecific antiserum by immunoaffinity purification.

    Stérilité

    Sterile filtered

    Immunogène

    Immunogen: This affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to a N-terminal region near amino acids 1-25 of human FANCG protein.

    Immunogen Type: Conjugated Peptide

    Isotype

    IgG
  • Indications d'application

    Immunohistochemistry Dilution: 1:500 - 1:2,000

    Application Note: This affinity purified antibody has been tested for use in ELISA, immunohistochemistry and by western blot.  Specific conditions for reactivity should be optimized by the end user. Expect a band approximately 69 kDa in size corresponding to FANCG by western blotting in the appropriate human tissue.

    Western Blot Dilution: 1:500 - 1:2,000

    ELISA Dilution: 1:10,000 - 1:50,000

    Other: User Optimized

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.93 mg/mL

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.01 % (w/v) Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Date de péremption

    12 months
  • Antigène

    FANCG (Fanconi Anemia Complementation Group G (FANCG))

    Autre désignation

    FANCG

    Sujet

    Background: FANCG (also called Protein FACG or DNA-repair protein XRCC9) is involved in DNA repair, perhaps specifically with post-replication repair or a cell cycle checkpoint function. FANCG may also be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. This protein may also function as a tumor suppressor gene. FANCG belongs to the multi-subunit Fanconi Anemia (FA) complex composed of FANCA, FANCB, FANCC, FANCE, FANCF, FANCG, FANCL/PHF9 and FANCM. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. FANCG is mainly found within the nucleus although some protein is localized in the cytoplasm.  This protein is highly expressed in testis and thymus and is also found in lymphoblasts. 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.

    ID gène

    2189, 4759336

    UniProt

    O15287

    Pathways

    Réparation de l'ADN
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