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WBSCR27 antibody (AA 1-245)

WBSCR27 Reactivity: Human WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7271366
  • Target See all WBSCR27 Antibodies
    WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))
    Binding Specificity
    • 8
    • 8
    • 7
    • 1
    AA 1-245
    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
    • 13
    • 13
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purpose
    WBSCR27 Rabbit pAb
    Sequence
    MAQEEGGSLP EVRARVRAAH GIPDLAQKLH FYDRWAPDYD QDVATLLYRA PRLAVDCLTQ ALPGPPHSAL ILDVACGTGL VAAELRAPGF LQLHGVDGSP GMLEQAQAPG LYQRLSLCTL GQEPLPSPEG TFDAVLIVGA LSDGQVPCNA IPELHVTKPG GLVCLTTRTN SSNLQYKEAL EATLDRLEQA GMWEGLVAWP VDRLWTAGSW LPPSWRWYPA SLPRMASSPA LSTCTESGRR PRLRK
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 1-245 of human WBSCR27 (NP_689772.2).
    Isotype
    IgG
  • Application Notes
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))
    Alternative Name
    WBSCR27 (WBSCR27 Products)
    Synonyms
    methyltransferase like 27 antibody, METTL27 antibody
    Background
    This gene 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.,METTL27,WBSCR27,Cell Biology & Developmental Biology,WBSCR27
    Molecular Weight
    26kDa
    Gene ID
    155368
    UniProt
    Q8N6F8
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