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

L’anticorps Lapin Polyclonal anti- a été validé pour WB et IP. Il convient pour détecter dans des échantillons de Humain.
N° du produit ABIN7450766

Aperçu rapide pour Spectrin, Beta, Non-erythrocytic 2 (SPTBN2) (AA 2340-2390) anticorps (ABIN7450766)

Antigène

Voir toutes Spectrin, Beta, Non-erythrocytic 2 (SPTBN2) Anticorps
Spectrin, Beta, Non-erythrocytic 2 (SPTBN2)

Reactivité

  • 110
  • 35
  • 33
  • 1
Humain

Hôte

  • 67
  • 43
Lapin

Clonalité

  • 100
  • 10
Polyclonal

Conjugué

  • 39
  • 9
  • 9
  • 9
  • 9
  • 9
  • 9
  • 9
  • 8
Inconjugué

Application

  • 107
  • 73
  • 66
  • 63
  • 29
  • 20
  • 14
  • 7
  • 5
  • 4
  • 3
Western Blotting (WB), Immunoprecipitation (IP)
  • Épitope

    • 98
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2340-2390

    Fonction

    Rabbit anti-SPTBN2/SCA5 Antibody, Affinity Purified

    Homologie

    Rat

    Purification

    Affinity Purified

    Immunogène

    between AA 2340 and 2390

    Isotype

    IgG
  • 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

    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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