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PNKD antibody

PNKD Reactivity: Human, Mouse, Rat WB, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6293999
  • Target See all PNKD Antibodies
    PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))
    Reactivity
    • 22
    • 19
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 30
    • 1
    Rabbit
    Clonality
    • 30
    Polyclonal
    Conjugate
    • 17
    • 4
    • 3
    • 3
    • 2
    • 2
    This PNKD antibody is un-conjugated
    Application
    • 24
    • 22
    • 17
    • 3
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human PNKD
    Isotype
    IgG
    Top Product
    Discover our top product PNKD Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    IF 1:50 - 1:200
    Comment

    Isoform 1 is only expressed in the brain, Isoform 2 is ubiquitously detected with highest expression in skeletal muscle and detected in myocardial myofibrils, Variant Val-7 and Val-9 are detected in the brain only

    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Target
    PNKD (Paroxysmal Nonkinesigenic Dyskinesia (PNKD))
    Alternative Name
    PNKD (PNKD Products)
    Synonyms
    BRP17 antibody, DYT8 antibody, FPD1 antibody, KIPP1184 antibody, MR-1 antibody, MR1 antibody, PDC antibody, PKND1 antibody, TAHCCP2 antibody, 2210013N15Rik antibody, 2810403H05Rik antibody, AI854243 antibody, Brp17 antibody, MNCb-5687 antibody, Tahccp2 antibody, paroxysmal nonkinesigenic dyskinesia antibody, paroxysmal nonkinesiogenic dyskinesia antibody, PNKD antibody, Pnkd antibody
    Background
    This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    42.876 kDa
    Gene ID
    25953
    UniProt
    Q8N490
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