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NPAP1 anticorps (AA 800-850) (Cy3)

NPAP1 Reactivité: Humain WB, IF (p) Hôte: Lapin Polyclonal Cy3
N° du produit ABIN1421591
  • Antigène Voir toutes NPAP1 Anticorps
    NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
    Épitope
    • 14
    • 1
    AA 800-850
    Reactivité
    Humain
    Hôte
    • 22
    Lapin
    Clonalité
    • 22
    Polyclonal
    Conjugué
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NPAP1 est conjugé à/à la Cy3
    Application
    • 15
    • 12
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
     Réactivité croisée
    Humain
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human NPAP1
    Isotype
    IgG
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    Discover our top product NPAP1 Anticorps primaire
  • Indications d'application
    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.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Date de péremption
    12 months
  • Antigène
    NPAP1 (Nuclear Pore Associated Protein 1 (NPAP1))
    Autre désignation
    NPAP1 (NPAP1 Produits)
    Synonymes
    anticorps C15orf2, anticorps nuclear pore associated protein 1, anticorps NPAP1
    Sujet

    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.

    ID gène
    23742
    UniProt
    Q9NZP6
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