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FKBP6 antibody

FKBP6 Reactivity: Human, Mouse, Rat IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7011509
  • Target See all FKBP6 Antibodies
    FKBP6 (FK506 Binding Protein 6, 36kDa (FKBP6))
    Reactivity
    • 35
    • 7
    • 7
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 32
    • 3
    Rabbit
    Clonality
    • 32
    • 3
    Polyclonal
    Conjugate
    • 15
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This FKBP6 antibody is un-conjugated
    Application
    • 24
    • 20
    • 8
    • 5
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human FKBP6 (NP_003593.3).
    Isotype
    IgG
    Top Product
    Discover our top product FKBP6 Primary Antibody
  • Application Notes
    IHC 1:50-1:200 IF 1:50-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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
    FKBP6 (FK506 Binding Protein 6, 36kDa (FKBP6))
    Alternative Name
    FKBP6 (FKBP6 Products)
    Synonyms
    1700008G22Rik antibody, 36kDa antibody, AU017274 antibody, D5Ertd724e antibody, FKBP-36 antibody, FKBP-6 antibody, PPiase antibody, FKBP36 antibody, FK506 binding protein 6 antibody, FK506 binding protein 6 L homeolog antibody, Fkbp6 antibody, fkbp6.L antibody, FKBP6 antibody
    Background
    The protein encoded by this gene is a cis-trans peptidyl-prolyl isomerase that may function in immunoregulation and basic cellular processes involving protein folding and trafficking. This gene is located in a chromosomal region that is deleted in Williams-Beuren syndrome. Defects in this gene may cause male infertility. There are multiple pseudogenes for this gene located nearby on chromosome 7. Alternative splicing results in multiple transcript variants.
    Gene ID
    8468
    UniProt
    O75344
    Pathways
    M Phase
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