Strumpellin Antikörper (AA 380-530)

Produktnummer ABIN7271349

Produktdetails anti-Strumpellin Antikörper

Target: Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))

Bindungsspezifität: AA 380-530

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Strumpellin Antikörper ist unkonjugiert

Applikation: 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

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Details zu Strumpellin

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