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NSUN5P2 anticorps

NSUN5P2 Reactivité: Humain WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2463242
  • Antigène Tous les produits NSUN5P2
    NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
    Reactivité
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 3
    Lapin
    Clonalité
    • 3
    Polyclonal
    Conjugué
    • 3
    Cet anticorp NSUN5P2 est non-conjugé
    Application
    • 3
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Antibody is purified by protein A chromatography method.
    Immunogène
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NSUN5C.
  • Indications d'application
    NSUN5C antibody can be used for detection of NSUN5C by ELISA at 1:312500. NSUN5C antibody can be used for detection of NSUN5C by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    Concentration
    1 mg/mL
    Buffer
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    Conseil sur la manipulation
    As with any antibody avoid repeat freeze-thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store NSUN5C antibody at -20 °C.
  • Antigène
    NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
    Autre désignation
    NSUN5C (NSUN5P2 Produits)
    Synonymes
    anticorps NOL1R2, anticorps NSUN5C, anticorps WBSCR20B, anticorps WBSCR20C, anticorps NOP2/Sun RNA methyltransferase family member 5 pseudogene 2, anticorps NSUN5P2
    Sujet
    NSUN5C gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder.This gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
    Poids moléculaire
    34 kDa
    ID gène
    260294
    NCBI Accession
    NP_115534
    UniProt
    Q63ZY6
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