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FUNDC2 anticorps

FUNDC2 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246850
  • Antigène Voir toutes FUNDC2 Anticorps
    FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))
    Reactivité
    • 15
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 14
    • 3
    Lapin
    Clonalité
    • 15
    • 2
    Polyclonal
    Conjugué
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp FUNDC2 est non-conjugé
    Application
    • 10
    • 4
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human FUNDC2
    Isotype
    IgG
    Top Product
    Discover our top product FUNDC2 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.72 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))
    Autre désignation
    FUNDC2 (FUNDC2 Produits)
    Synonymes
    anticorps DC44, anticorps HCBP6, anticorps HCC3, anticorps PD03104, anticorps 4833415N24Rik, anticorps FUN14 domain containing 2, anticorps FUNDC2, anticorps Fundc2
    Sujet
    FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
    UniProt
    Q9BWH2
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