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Caveolin 3 anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement Caveolin 3 dans WB et IHC. Il présente une réactivité envers Humain.
N° du produit ABIN7266157

Aperçu rapide pour Caveolin 3 anticorps (ABIN7266157)

Antigène

Voir toutes Caveolin 3 (CAV3) Anticorps
Caveolin 3 (CAV3)

Reactivité

  • 33
  • 17
  • 16
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 32
  • 3
  • 1
Lapin

Clonalité

  • 25
  • 11
Monoclonal

Conjugué

  • 22
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp Caveolin 3 est non-conjugé

Application

  • 20
  • 8
  • 8
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC)
  • Fonction

    Caveolin-3 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human Caveolin-3

    Isotype

    IgG
  • Indications d'application

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

    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

    Caveolin 3 (CAV3)

    Autre désignation

    CAV3

    Sujet

    This gene encodes a caveolin family member, which functions as a component of the caveolae plasma membranes found in most cell types. Caveolin proteins are proposed to be scaffolding proteins for organizing and concentrating certain caveolin-interacting molecules. Mutations identified in this gene lead to interference with protein oligomerization or intra-cellular routing, disrupting caveolae formation and resulting in Limb-Girdle muscular dystrophy type-1C (LGMD-1C), hyperCKemia or rippling muscle disease (RMD). Alternative splicing has been identified for this locus, with inclusion or exclusion of a differentially spliced intron. In addition, transcripts utilize multiple polyA sites and contain two potential translation initiation sites. [provided by RefSeq, Jul 2008],LGMD1C, LQT9, VIP-21, VIP21,Endocrine & Metabolism,ErbB-HER Signaling Pathway,Insulin Receptor Signaling Pathway,Signal Transduction,CAV3

    Poids moléculaire

    17kDa

    ID gène

    859

    UniProt

    P56539

    Pathways

    Carbohydrate Homeostasis, Regulation of Muscle Cell Differentiation, Regulation of Cell Size, Skeletal Muscle Fiber Development, Negative Regulation of Transporter Activity
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