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Reelin Antikörper

RELN Reaktivität: Human WB, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7269893
  • Target Alle Reelin (RELN) Antikörper anzeigen
    Reelin (RELN)
    Reaktivität
    • 36
    • 24
    • 9
    Human
    Wirt
    • 35
    • 10
    • 2
    • 1
    Kaninchen
    Klonalität
    • 29
    • 19
    Polyklonal
    Konjugat
    • 25
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser Reelin Antikörper ist unkonjugiert
    Applikation
    • 29
    • 23
    • 14
    • 9
    • 8
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Verwendungszweck
    RELN Rabbit pAb
    Kreuzreaktivität
    Human, Maus, Ratte
    Produktmerkmale
    Polyclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant protein of human RELN.
    Isotyp
    IgG
    Top Product
    Discover our top product RELN Primärantikörper
  • Applikationshinweise
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Reelin (RELN)
    Andere Bezeichnung
    RELN (RELN Produkte)
    Synonyme
    LIS2 antikoerper, PRO1598 antikoerper, RL antikoerper, reeler antikoerper, rl antikoerper, Reelen antikoerper, Rl antikoerper, reln antikoerper, RELN antikoerper, MGC172539 antikoerper, reelin antikoerper, reelin L homeolog antikoerper, RELN antikoerper, Reln antikoerper, reln antikoerper, reln.L antikoerper, LOC579060 antikoerper
    Hintergrund
    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
    Gen-ID
    5649
    UniProt
    P78509
    Pathways
    Synaptic Membrane
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