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SPTA1 anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement SPTA1 dans WB, IHC et ELISA. Il présente une réactivité envers Humain et Souris.
N° du produit ABIN7248185

Aperçu rapide pour SPTA1 anticorps (ABIN7248185)

Antigène

Voir toutes SPTA1 Anticorps
SPTA1 (Spectrin alpha 1, Erythrocytic (SPTA1))

Reactivité

  • 63
  • 12
  • 5
  • 1
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 37
  • 27
Lapin

Clonalité

  • 51
  • 13
Polyclonal

Conjugué

  • 25
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SPTA1 est non-conjugé

Application

  • 46
  • 44
  • 36
  • 8
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Synthetic peptide of human SPTA1

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000, IHC 1:60-1:450, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.7 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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.
  • Antigène

    SPTA1 (Spectrin alpha 1, Erythrocytic (SPTA1))

    Autre désignation

    SPTA1

    Sujet

    Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton, and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. It is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement. This gene is one member of a family of alpha-spectrin genes. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms weaker tetramer interactions than non-erythrocytic alpha spectrin, which may increase the plasma membrane elasticity and deformability of red blood cells. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis type 2, pyropoikilocytosis, and spherocytic hemolytic anemia.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 280 kDa

    UniProt

    P02549

    Pathways

    Regulation of Actin Filament Polymerization
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