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Spectrin, Beta, Non-erythrocytic 2 (SPTBN2) (AA 2340-2390) anticorps

SPTBN2 Reactivité: Humain WB, IP Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7450766
  • Antigène Voir toutes Spectrin, Beta, Non-erythrocytic 2 (SPTBN2) Anticorps
    Spectrin, Beta, Non-erythrocytic 2 (SPTBN2)
    Épitope
    • 50
    • 3
    • 2
    • 1
    • 1
    AA 2340-2390
    Reactivité
    • 60
    • 23
    • 21
    • 1
    Humain
    Hôte
    • 44
    • 16
    Lapin
    Clonalité
    • 52
    • 8
    Polyclonal
    Conjugué
    • 32
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    • 4
    Inconjugué
    Application
    • 58
    • 46
    • 44
    • 42
    • 19
    • 14
    • 7
    • 5
    • 3
    • 3
    Western Blotting (WB), Immunoprecipitation (IP)
    Fonction
    Rabbit anti-SPTBN2/SCA5 Antibody, Affinity Purified
    Homologie
    Rat
    Purification
    Affinity Purified
    Immunogène
    between AA 2340 and 2390
    Isotype
    IgG
    Top Product
    Discover our top product SPTBN2 Anticorps primaire
  • Indications d'application

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions
    For Research Use only
  • Concentration
    200 μg/mL
    Buffer
    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
    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
    4 °C
    Date de péremption
    12 months
  • Antigène
    Spectrin, Beta, Non-erythrocytic 2 (SPTBN2)
    Autre désignation
    SPTBN2/SCA5 (SPTBN2 Produits)
    Synonymes
    anticorps Spnb3, anticorps mKIAA0302, anticorps GTRAP41, anticorps SCA5, anticorps spectrin beta, non-erythrocytic 2, anticorps spectrin, beta, non-erythrocytic 2, anticorps Sptbn2, anticorps SPTBN2
    Sujet
    Background: SPTBN2/SCA5 is a member of the beta spectrin gene family and a subunit of the spectrin cytoskeletal scaffolding protein that links the plasma membrane to cytoskeletal actin and functions in cellular shape and organelle organization. SPTBN2/SCA5 has been identified as a Golgi- and vesicle-associated spectrin. Mutations in SPTBN2/SCA5 cause spinocerebellar ataxia type 5 (SCA5), an autosomal dominant disease characterized by progressive incoordination of gait, hand, speech, and eye movements.
    ID gène
    6712
    NCBI Accession
    NP_008877
    UniProt
    O15020
    Pathways
    Regulation of Actin Filament Polymerization, Synaptic Vesicle Exocytosis
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