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ZNF703 anticorps

ZNF703 Reactivité: Humain, Souris, Rat IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7257802
  • Antigène Voir toutes ZNF703 Anticorps
    ZNF703 (Zinc Finger Protein 703 (ZNF703))
    Reactivité
    • 47
    • 7
    • 7
    • 6
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 44
    • 2
    • 1
    Lapin
    Clonalité
    • 45
    • 2
    Polyclonal
    Conjugué
    • 19
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp ZNF703 est non-conjugé
    Application
    • 35
    • 17
    • 13
    • 13
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human ZNF703 (NP_079345.1).
    Isotype
    IgG
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    ZNF703 (Zinc Finger Protein 703 (ZNF703))
    Autre désignation
    ZNF703 (ZNF703 Produits)
    Sujet
    ZNF703 (zinc finger protein 703) is a 590 amino acid nuclear protein that contains one C2H2-type zinc finger and is thought to play a role in transcriptional regulation. Multiple isoforms of ZNF703 exist due to alternative splicing events. The gene encoding ZNF703 maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
    ID gène
    80139
    UniProt
    Q9H7S9
    Pathways
    Cell-Cell Junction Organization
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