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NPAP1 antibody (AA 800-850) (AbBy Fluor® 647)

NPAP1 Reactivity: Human WB, IF (p) Host: Rabbit Polyclonal AbBy Fluor® 647
Catalog No. ABIN1403724
  • Target See all NPAP1 Antibodies
    NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
    Binding Specificity
    • 14
    • 1
    AA 800-850
    Reactivity
    Human
    Host
    • 22
    Rabbit
    Clonality
    • 22
    Polyclonal
    Conjugate
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NPAP1 antibody is conjugated to AbBy Fluor® 647
    Application
    • 15
    • 12
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Cross-Reactivity
    Human
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human NPAP1
    Isotype
    IgG
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    Discover our top product NPAP1 Primary Antibody
  • Application Notes
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Expiry Date
    12 months
  • Target
    NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
    Alternative Name
    NPAP1 (NPAP1 Products)
    Synonyms
    C15orf2 antibody, nuclear pore associated protein 1 antibody, NPAP1 antibody
    Background

    Synonyms: NPAP1, NPAP 1, NPAP-1, Nuclear pore associated protein 1, NPAP1_HUMAN, C15orf2.

    Background: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.

    Gene ID
    23742
    UniProt
    Q9NZP6
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