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Strumpellin anticorps (C-Term)

WASHC5 Reactivité: Humain, Souris, Rat WB, EIA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1450091
  • Antigène Voir toutes Strumpellin (WASHC5) Anticorps
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Épitope
    • 2
    • 1
    • 1
    • 1
    C-Term
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 5
    Lapin
    Clonalité
    • 5
    Polyclonal
    Conjugué
    • 5
    Cet anticorp Strumpellin est non-conjugé
    Application
    • 5
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Purification
    Affinity chromatography purified via peptide column
    Immunogène
    A 19 amino acid synthetic peptide near the carboxy terminus of Human Strumpellin
    Isotype
    IgG
    Top Product
    Discover our top product WASHC5 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Concentration
    1.0 mg/mL
    Buffer
    PBS containing 0.02 % Sodium Azide as preservative
    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.
    Conseil sur la manipulation
    Avoid repeated freezing and thawing.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Autre désignation
    Strumpellin (WASHC5 Produits)
    Synonymes
    anticorps SPG8, anticorps AL022848, anticorps C76463, anticorps Kiaa0196, anticorps mKIAA0196, anticorps strumpellin, anticorps WASH complex subunit 5, anticorps WASHC5, anticorps washc5, anticorps Washc5
    Sujet
    Strumpellin is a ubiquitously expressed, multi-transmembrane and spectrin-repeat-containing protein. It is named for Strumpell disease, a progressive upper-motor neurodegenerative disease termed hereditary spastic paraplegia (HSP). The Strumpellin gene maps to the eighth HSP locus (SPG8) on chromosome 8p24.13. Three families liked to this locus have mutations in the Strumpellin gene, rescue studies of zebrafish with decreased Strumpellin expression with Strumpellin mRNA containing these mutations showed impaired normal function of this protein. Recent studies suggest that Strumpellin may also be involved in protein aggregation diseases.Synonyms: KIAA0196
    ID gène
    9897
    NCBI Accession
    NP_055661
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