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SNX29 anticorps

RUNDC2A Reactivité: Humain IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7192586
  • Antigène Tous les produits SNX29 (RUNDC2A)
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    Reactivité
    • 29
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 27
    • 2
    Lapin
    Clonalité
    • 27
    • 2
    Polyclonal
    Conjugué
    • 12
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp SNX29 est non-conjugé
    Application
    • 21
    • 17
    • 16
    • 3
    • 2
    Immunohistochemistry (IHC), ELISA
     Réactivité croisée
    Humain, Souris
    Purification
    Antigen affinity purification
    Immunogène
    Synthetic peptide of Human SNX29
    Isotype
    IgG
  • Indications d'application
    ELISA:1:1000-1:2000, IHC:1:20-1:100,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Stockage commentaire
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Antigène
    SNX29 (RUNDC2A) (RUN Domain Containing 2A (RUNDC2A))
    Autre désignation
    SNX29 (RUNDC2A Produits)
    Synonymes
    anticorps RUNDC2A, anticorps 4933437K13Rik, anticorps ENSMUSG00000079738, anticorps Gm11170, anticorps Gm1737, anticorps Gm930, anticorps Rundc2a, anticorps RGD1565890, anticorps A-388D4.1, anticorps RUN domain containing 2A, anticorps sorting nexin 29, anticorps sorting nexin-29, anticorps RUNDC2A, anticorps Snx29, anticorps SNX29, anticorps LOC104975843
    Sujet

    Background: SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

    Aliases: SNX29 antibody, RUNDC2A antibody, Sorting nexin-29 antibody, RUN domain-containing protein 2A antibody

    UniProt
    Q8TEQ0
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