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EBNA1BP2 antibody

EBNA1BP2 Reactivity: Human, Mouse, Rat IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7264749
  • Target See all EBNA1BP2 Antibodies
    EBNA1BP2 (EBNA1 Binding Protein 2 (EBNA1BP2))
    Reactivity
    • 29
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 29
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 12
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This EBNA1BP2 antibody is un-conjugated
    Application
    • 22
    • 15
    • 1
    • 1
    • 1
    • 1
    Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human EBNA1BP2 (NP_006815.2).
    Isotype
    IgG
    Top Product
    Discover our top product EBNA1BP2 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
    EBNA1BP2 (EBNA1 Binding Protein 2 (EBNA1BP2))
    Alternative Name
    EBNA1BP2 (EBNA1BP2 Products)
    Synonyms
    Ebp2 antibody, fa12d07 antibody, ebna1bp2l antibody, wu:fa12d07 antibody, ebp2 antibody, nobp antibody, EBP2 antibody, NOBP antibody, P40 antibody, 1810014B19Rik antibody, AA537058 antibody, B830003A16Rik antibody, C81321 antibody, Nobp antibody, p40 antibody, EBNA1 binding protein 2 antibody, microRNA 6733 antibody, Ebna1bp2 antibody, ebna1bp2 antibody, MIR6733 antibody, EBNA1BP2 antibody, ebna1bp2-a antibody
    Background
    EBNA1BP2 (EBNA1 Binding Protein 2) is a Protein Coding gene. Diseases associated with EBNA1BP2 include Robinow Syndrome, Autosomal Dominant 1 and Intracranial Hypotension.
    Gene ID
    10969
    UniProt
    Q99848
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