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FKBP1A anticorps

L’anticorps Lapin Monoclonal anti-FKBP1A a été validé pour WB. Il convient pour détecter FKBP1A dans des échantillons de Humain.
N° du produit ABIN7267211

Aperçu rapide pour FKBP1A anticorps (ABIN7267211)

Antigène

Voir toutes FKBP1A Anticorps
FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))

Reactivité

  • 62
  • 30
  • 22
  • 6
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 58
  • 12
Lapin

Clonalité

  • 50
  • 20
Monoclonal

Conjugué

  • 32
  • 9
  • 8
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp FKBP1A est non-conjugé

Application

  • 40
  • 24
  • 17
  • 12
  • 11
  • 11
  • 6
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    FKBP12 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human FKBP12

    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

    FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))

    Autre désignation

    FKBP1A

    Sujet

    The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed. [provided by RefSeq, Sep 2008],FKBP-12, FKBP-1A, FKBP1, FKBP12, PKC12, PKCI2, PPIASE,Epigenetic writers and erasers of core Histones,Epigenetic writers and erasers of core Histones_other,Epigenetics & Nuclear Signaling,Immunology & Inflammation,mTOR Signaling Pathway,PI3K-Akt Signaling Pathway,PI3K-Akt Signaling Pathway_Regulator of mTOR complex function,Signal Transduction,TGF-b-Smad Signaling Pathway_Regulator,Translation Control,Translational Control_Regulation of eIF4 and p70 S6 Kinase,FKBP1A

    Poids moléculaire

    12kDa

    ID gène

    2280

    UniProt

    P62942

    Pathways

    Negative Regulation of Transporter Activity, Methionine Biosynthetic Process
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