Strumpellin anticorps (AA 380-530)

N° du produit ABIN7271349

Cet anticorps anti-Strumpellin est un anticorps Lapin Polyclonal détectant Strumpellin dans WB et IHC. Adapté pour Humain.

Aperçu rapide pour Strumpellin anticorps (AA 380-530) (ABIN7271349)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Strumpellin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-Strumpellin anticorps

Épitope: AA 380-530

Fonction: KIAA0196 Rabbit pAb

Réactivité croisée: Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 380-530 of human KIAA0196 (NP_055661.3).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Restrictions: For Research Use only

Stockage

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.

Détails sur Strumpellin

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

Autre désignation: KIAA0196

Sujet: 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

ID gène: 9897

UniProt: Q12768