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NSUN5 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects NSUN5 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN2774485

Quick Overview for NSUN5 antibody (C-Term) (ABIN2774485)

Target

See all NSUN5 Antibodies
NSUN5 (NOP2/Sun Domain Family, Member 5 (NSUN5))

Reactivity

  • 24
  • 2
  • 1
Human

Host

  • 24
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NSUN5 antibody is un-conjugated

Application

  • 21
  • 13
  • 13
  • 10
  • 3
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

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

    Sequence

    ASPETTLSSG FFVAVIERVE VPSSASQAKA SAPERTPSPA PKRKKRQQRA

    Predicted Reactivity

    Human: 100%

    Characteristics

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

    Purification

    Affinity Purified

    Immunogen

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

    Optimal working dilutions should be determined experimentally by the investigator.

    Comment

    Antigen size: 466 AA

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    Lot specific

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    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))

    Alternative Name

    NSUN5

    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 Interaction Partner: SUMO1, UBC, NEDD8, CDK13, UBD,
    Protein Size: 466

    Molecular Weight

    50 kDa

    Gene ID

    55695

    NCBI Accession

    NM_148956, NP_683759
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