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WB analysis of various sample lysates using GTX33582 WBSCR22 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX33582 WBSCR22 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX33582 WBSCR22 antibody. Dilution : 1:1000 Loading : 25microg per lane

WBSCR22 antibody

GTX33582
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetBUD23
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Overview

  • Supplier
    GeneTex
  • Product Name
    WBSCR22 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:100. IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID114049
  • Target name
    BUD23
  • Target description
    BUD23 rRNA methyltransferase and ribosome maturation factor
  • Target synonyms
    bud site selection protein 23 homolog; HASJ4442; HUSSY-3; MERM1; metastasis-related methyltransferase 1; PP3381; probable 18S rRNA (guanine-N(7))-methyltransferase; ribosome biogenesis methyltransferase WBSCR22; rRNA methyltransferase and ribosome maturation factor; WBMT; WBSCR22; Williams-Beuren candidate region putative methyltransferase; Williams-Beuren syndrome chromosomal region 22 protein; Williams-Beuren syndrome chromosome region 22
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO43709
  • Protein Name
    Probable 18S rRNA (guanine-N(7))-methyltransferase
  • Scientific Description
    This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Immunofluorescent staining data of BUD23 using Anti-WBSCR22 BUD23 Antibody (A32249). Immunofluorescence analysis of MCF7 cell using WBSCR22 antibody. Blue: DAPI for nuclear staining.
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