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CLDND2 anticorps

CLDND2 Reactivité: Humain, Souris ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7244468
  • Antigène Voir toutes CLDND2 Anticorps
    CLDND2 (Claudin Domain Containing 2 (CLDND2))
    Reactivité
    Humain, Souris
    Hôte
    • 9
    • 2
    Lapin
    Clonalité
    • 11
    Polyclonal
    Conjugué
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp CLDND2 est non-conjugé
    Application
    • 4
    • 2
    • 2
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human CLDND2
    Isotype
    IgG
    Top Product
    Discover our top product CLDND2 Anticorps primaire
  • Indications d'application
    IHC 1:30-150, ELISA 1:2000-10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    CLDND2 (Claudin Domain Containing 2 (CLDND2))
    Autre désignation
    CLDND2 (CLDND2 Produits)
    Synonymes
    anticorps 1700071E18Rik, anticorps RGD1566413, anticorps claudin domain containing 2, anticorps CLDND2, anticorps Cldnd2
    Sujet
    CLDND2 (claudin domain containing 2) is a 167 amino acid multi-pass membrane protein that belongs to the PMP-22/EMP/MP20 family and is encoded by a gene that maps to human chromosome 19q13.33. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2 % of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19.
    NCBI Accession
    NP_689566
    UniProt
    Q8NHS1
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