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Filamin A anticorps

Cet anticorps anti-Filamin A est un anticorps Lapin Polyclonal détectant Filamin A dans WB, IHC et ELISA. Adapté pour Humain et Souris.
N° du produit ABIN7237020

Aperçu rapide pour Filamin A anticorps (ABIN7237020)

Antigène

Voir toutes Filamin A (FLNA) Anticorps
Filamin A (FLNA) (Filamin A, alpha (FLNA))

Reactivité

  • 105
  • 33
  • 23
  • 3
  • 2
  • 1
Humain, Souris

Hôte

  • 96
  • 9
  • 1
Lapin

Clonalité

  • 85
  • 21
Polyclonal

Conjugué

  • 47
  • 7
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp Filamin A est non-conjugé

Application

  • 55
  • 33
  • 30
  • 28
  • 28
  • 24
  • 16
  • 12
  • 9
  • 7
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human FLNA

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000, IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    Filamin A (FLNA) (Filamin A, alpha (FLNA))

    Autre désignation

    FLNA

    Sujet

    The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    281 kDa

    NCBI Accession

    NP_001104026

    UniProt

    P21333

    Pathways

    TCR Signaling, Maintenance of Protein Location
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