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FKBP1A Antikörper

Der Kaninchen Monoklonal Anti-FKBP1A-Antikörper wurde für WB validiert. Er ist geeignet, FKBP1A in Proben von Human zu detektieren.
Produktnummer ABIN7267211

Kurzübersicht für FKBP1A Antikörper (ABIN7267211)

Target

Alle FKBP1A Antikörper anzeigen
FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))

Reaktivität

  • 65
  • 30
  • 22
  • 7
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Wirt

  • 64
  • 10
Kaninchen

Klonalität

  • 56
  • 18
Monoklonal

Konjugat

  • 36
  • 10
  • 9
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Dieser FKBP1A Antikörper ist unkonjugiert

Applikation

  • 44
  • 31
  • 19
  • 16
  • 11
  • 9
  • 8
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Verwendungszweck

    FKBP12 Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human FKBP12

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

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

    Andere Bezeichnung

    FKBP1A

    Hintergrund

    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

    Molekulargewicht

    12kDa

    Gen-ID

    2280

    UniProt

    P62942

    Pathways

    Negative Regulation of Transporter Activity, Methionine Biosynthetic Process
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