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WBSCR27 antibody (N-Term)

WBSCR27 Reactivity: Human WB, IHC (p) Host: Rabbit Polyclonal RB27437 unconjugated
Catalog No. ABIN654505
  • Target See all WBSCR27 Antibodies
    WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))
    Binding Specificity
    • 7
    • 7
    • 7
    • 2
    AA 5-34, N-Term
    Reactivity
    • 17
    • 1
    Human
    Host
    • 16
    • 1
    Rabbit
    Clonality
    • 16
    • 1
    Polyclonal
    Conjugate
    • 7
    • 2
    • 2
    • 2
    • 2
    • 2
    This WBSCR27 antibody is un-conjugated
    Application
    • 17
    • 14
    • 13
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This WBSCR27 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human WBSCR27.
    Clone
    RB27437
    Isotype
    Ig Fraction
    Top Product
    Discover our top product WBSCR27 Primary Antibody
  • Application Notes
    WB: 1:1000. IHC-P: 1:50~100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Storage Comment
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Expiry Date
    6 months
  • Target
    WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))
    Alternative Name
    WBSCR27 (WBSCR27 Products)
    Synonyms
    methyltransferase like 27 antibody, METTL27 antibody
    Background
    WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23.
    Molecular Weight
    26522
    Gene ID
    155368
    NCBI Accession
    NP_689772
    UniProt
    Q8N6F8
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