Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

NOP2/Sun Domain Family, Member 5 (NSUN5) (C-Term) Peptide

NSUN5 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN1541844
  • Target See all NSUN5 products
    NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))
    Protein Region
    C-Term
    Origin
    Human
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Sequence
    ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-NSUN5 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))
    Synonyms
    RGD1309268 Peptide, wu:fc49f12 Peptide, zgc:66176 Peptide, zgc:77183 Peptide, 9830109N13Rik Peptide, AI326939 Peptide, Nol1r Peptide, Wbscr20 Peptide, Wbscr20a Peptide, NOL1 Peptide, NOL1R Peptide, NSUN5A Peptide, WBSCR20 Peptide, WBSCR20A Peptide, p120 Peptide, NOP2/Sun RNA methyltransferase family member 5 Peptide, NOP2/Sun domain family, member 5 Peptide, NOL1/NOP2/Sun domain family, member 5 Peptide, Nsun5 Peptide, nsun5 Peptide, NSUN5 Peptide
    Background
    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 Size: 466
    Molecular Weight
    50 kDa
    Gene ID
    55695
    NCBI Accession
    NM_148956, NP_683759
You are here:
Support