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TTBK2 antibody

TTBK2 Reactivity: Human IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7256994
  • Target See all TTBK2 Antibodies
    TTBK2 (tau Tubulin Kinase 2 (TTBK2))
    Reactivity
    • 46
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 43
    • 3
    Rabbit
    Clonality
    • 45
    • 1
    Polyclonal
    Conjugate
    • 22
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TTBK2 antibody is un-conjugated
    Application
    • 42
    • 22
    • 21
    • 13
    • 13
    • 13
    • 8
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human TTBK2 (NP_775771.3).
    Isotype
    IgG
    Top Product
    Discover our top product TTBK2 Primary Antibody
  • Application Notes
    IF 1:50-1:200
    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
    TTBK2 (tau Tubulin Kinase 2 (TTBK2))
    Alternative Name
    TTBK2 (TTBK2 Products)
    Synonyms
    ttbk antibody, MGC146331 antibody, 2610507N02Rik antibody, AI326283 antibody, B930008N24Rik antibody, TTK antibody, Ttbk antibody, Ttbk1 antibody, mKIAA0847 antibody, SCA11 antibody, TTBK antibody, tau tubulin kinase 2 antibody, TTBK2 antibody, ttbk2 antibody, Ttbk2 antibody
    Background
    This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11), a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.
    Gene ID
    146057
    UniProt
    Q6IQ55
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