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SPTA1 anticorps

L’anticorps Lapin Monoclonal anti-SPTA1 a été validé pour WB. Il convient pour détecter SPTA1 dans des échantillons de Humain.
N° du produit ABIN7270517

Aperçu rapide pour SPTA1 anticorps (ABIN7270517)

Antigène

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

Reactivité

  • 63
  • 13
  • 5
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 37
  • 27
Lapin

Clonalité

  • 50
  • 14
Monoclonal

Conjugué

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

Application

  • 47
  • 44
  • 36
  • 9
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
Western Blotting (WB)
  • Fonction

    alpha 1 Spectrin Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human alpha 1 Spectrin

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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.
  • 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. [provided by RefSeq, Jul 2008],EL2, HPP, HS3, SPH3, SPTA,Blood,Blood_Blood Cell Antigens,Cardiovascular,Cell Biology & Developmental Biology,Cytoskeleton,Cytoskeleton_Microfilaments,Signal Transduction,SPTA1

    Poids moléculaire

    280kDa

    ID gène

    6708

    UniProt

    P02549

    Pathways

    Regulation of Actin Filament Polymerization
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