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NSUN5P2 antibody

NSUN5P2 Reactivity: Human WB, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2463242
  • Target See all NSUN5P2 products
    NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
    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
    • 1
    • 1
    Western Blotting (WB), ELISA
    Purification
    Antibody is purified by protein A chromatography method.
    Immunogen
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NSUN5C.
  • Application Notes
    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.
    Handling Advice
    As with any antibody avoid repeat freeze-thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store NSUN5C antibody 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.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.
    Molecular Weight
    34 kDa
    Gene ID
    260294
    NCBI Accession
    NP_115534
    UniProt
    Q63ZY6
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