Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Strumpellin Antikörper (AA 380-530)

WASHC5 Reaktivität: Human WB, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7271349
  • Target Alle Strumpellin (WASHC5) Antikörper anzeigen
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Bindungsspezifität
    • 3
    • 1
    • 1
    AA 380-530
    Reaktivität
    • 4
    • 4
    • 2
    Human
    Wirt
    • 5
    Kaninchen
    Klonalität
    • 5
    Polyklonal
    Konjugat
    • 5
    Dieser Strumpellin Antikörper ist unkonjugiert
    Applikation
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Verwendungszweck
    KIAA0196 Rabbit pAb
    Kreuzreaktivität
    Maus, Ratte
    Produktmerkmale
    Polyclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 380-530 of human KIAA0196 (NP_055661.3).
    Isotyp
    IgG
  • 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
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Andere Bezeichnung
    KIAA0196 (WASHC5 Produkte)
    Synonyme
    SPG8 antikoerper, AL022848 antikoerper, C76463 antikoerper, Kiaa0196 antikoerper, mKIAA0196 antikoerper, strumpellin antikoerper, WASH complex subunit 5 antikoerper, WASHC5 antikoerper, washc5 antikoerper, Washc5 antikoerper
    Hintergrund
    This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease, a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.,RTSC, SPG8, RTSC1, KIAA0196,KIAA0196
    Gen-ID
    9897
    UniProt
    Q12768
Sie sind hier:
Kundenservice