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Reelin anticorps

RELN Reactivité: Humain WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7269893
  • Antigène Voir toutes Reelin (RELN) Anticorps
    Reelin (RELN)
    Reactivité
    • 36
    • 24
    • 9
    Humain
    Hôte
    • 35
    • 10
    • 2
    • 1
    Lapin
    Clonalité
    • 29
    • 19
    Polyclonal
    Conjugué
    • 25
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Cet anticorp Reelin est non-conjugé
    Application
    • 29
    • 23
    • 14
    • 9
    • 8
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Fonction
    RELN Rabbit pAb
     Réactivité croisée
    Humain, Souris, Rat
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human RELN.
    Isotype
    IgG
    Top Product
    Discover our top product RELN Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    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
    Reelin (RELN)
    Autre désignation
    RELN (RELN Produits)
    Synonymes
    anticorps LIS2, anticorps PRO1598, anticorps RL, anticorps reeler, anticorps rl, anticorps Reelen, anticorps Rl, anticorps reln, anticorps RELN, anticorps MGC172539, anticorps reelin, anticorps reelin L homeolog, anticorps RELN, anticorps Reln, anticorps reln, anticorps reln.L, anticorps LOC579060
    Sujet
    This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008],ETL7,LIS2,PRO1598,RL,RELN,Cell Biology & Developmental Biology,Cell Adhesion,Neuroscience,Cell Type Marker,RELN
    ID gène
    5649
    UniProt
    P78509
    Pathways
    Synaptic Membrane
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