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FKBP1A antibody

FKBP1A Reactivity: Human WB Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7267211
  • Target See all FKBP1A Antibodies
    FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))
    Reactivity
    • 57
    • 28
    • 21
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    Host
    • 56
    • 8
    Rabbit
    Clonality
    • 49
    • 15
    Monoclonal
    Conjugate
    • 28
    • 9
    • 8
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    This FKBP1A antibody is un-conjugated
    Application
    • 34
    • 22
    • 18
    • 8
    • 8
    • 7
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    FKBP12 Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human FKBP12
    Isotype
    IgG
    Top Product
    Discover our top product FKBP1A Primary Antibody
  • Application Notes
    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.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    FKBP1A (FK506 Binding Protein 1A, 12kDa (FKBP1A))
    Alternative Name
    FKBP1A (FKBP1A Products)
    Background
    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
    Molecular Weight
    12kDa
    Gene ID
    2280
    UniProt
    P62942
    Pathways
    Negative Regulation of Transporter Activity, Methionine Biosynthetic Process
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