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NSUN5 Antikörper (C-Term)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch NSUN5 in WB. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN2774485

Kurzübersicht für NSUN5 Antikörper (C-Term) (ABIN2774485)

Target

Alle NSUN5 Antikörper anzeigen
NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

Reaktivität

  • 24
  • 2
  • 1
Human

Wirt

  • 24
Kaninchen

Klonalität

  • 24
Polyklonal

Konjugat

  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser NSUN5 Antikörper ist unkonjugiert

Applikation

  • 21
  • 13
  • 13
  • 10
  • 3
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 15
    • 5
    • 1
    • 1
    • 1
    C-Term

    Sequenz

    ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA

    Homologie

    Human: 100%

    Produktmerkmale

    This is a rabbit polyclonal antibody against NSUN5. It was validated on Western Blot.

    Aufreinigung

    Affinity Purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the C-terminal region of Human NSUN5
  • Applikationshinweise

    Optimal working dilutions should be determined experimentally by the investigator.

    Kommentare

    Antigen size: 466 AA

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    Lot specific

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

    Andere Bezeichnung

    NSUN5

    Hintergrund

    This gene encodes a member of the evolutionarily conserved NOL1/NOP2/Sun domain family. The encoded protein may function as a DNA methyltransferase in the nucleus. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.
    Alias Symbols: FLJ10267, MGC986, NOL1, NOL1R, NSUN5A, WBSCR20, WBSCR20A, p120
    Protein Interaction Partner: SUMO1, UBC, NEDD8, CDK13, UBD,
    Protein Size: 466

    Molekulargewicht

    50 kDa

    Gen-ID

    55695

    NCBI Accession

    NM_148956, NP_683759
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