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

NSUN5P2 antibody (Middle Region)

NSUN5P2 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN629781
  • Target See all NSUN5P2 products
    NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
    Binding Specificity
    Middle Region
    Reactivity
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 3
    Rabbit
    Clonality
    • 3
    Polyclonal
    Conjugate
    • 3
    This NSUN5P2 antibody is un-conjugated
    Application
    • 3
    • 2
    • 1
    Western Blotting (WB)
    Specificity
    NSUN5 C antibody was raised against the middle region of NSUN5
    Purification
    Purified
    Immunogen
    NSUN5 C antibody was raised using the middle region of NSUN5 corresponding to a region with amino acids PALPARPHRGLSTFPGAEHCLRASPKTTLSGGFFVAVIERVEMPTSASQA
  • Application Notes
    WB: 2.5 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    NSUN5C Blocking Peptide, catalog no. 33R-6965, is also available for use as a blocking control in assays to test for specificity of this NSUN5C antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of NSUN0 antibody in PBS
    Concentration
    Lot specific
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target
    NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
    Alternative Name
    NSUN5C (NSUN5P2 Products)
    Synonyms
    NOL1R2 antibody, NSUN5C antibody, WBSCR20B antibody, WBSCR20C antibody, NOP2/Sun RNA methyltransferase family member 5 pseudogene 2 antibody, NSUN5P2 antibody
    Background
    NSUN5C gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder.
    Molecular Weight
    34 kDa (MW of target protein)
You are here:
Support