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NPAP1 Antikörper (AA 800-850) (Alexa Fluor 488)

NPAP1 Reaktivität: Human WB, IF (p) Wirt: Kaninchen Polyclonal Alexa Fluor 488
Produktnummer ABIN1403722
  • Target Alle NPAP1 Antikörper anzeigen
    NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
    Bindungsspezifität
    • 14
    • 1
    AA 800-850
    Reaktivität
    Human
    Wirt
    • 16
    Kaninchen
    Klonalität
    • 16
    Polyklonal
    Konjugat
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser NPAP1 Antikörper ist konjugiert mit Alexa Fluor 488
    Applikation
    • 15
    • 12
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Kreuzreaktivität
    Human
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human NPAP1
    Isotyp
    IgG
    Top Product
    Discover our top product NPAP1 Primärantikörper
  • Applikationshinweise
    IF(IHC-P) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
    Andere Bezeichnung
    NPAP1 (NPAP1 Produkte)
    Synonyme
    C15orf2 antikoerper, nuclear pore associated protein 1 antikoerper, NPAP1 antikoerper
    Hintergrund

    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.

    Gen-ID
    23742
    UniProt
    Q9NZP6
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