
WB analysis of various sample lysates using GTX33582 WBSCR22 antibody. Dilution : 1:1000 Loading : 25microg per lane
WBSCR22 antibody
GTX33582
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetBUD23
Overview
- SupplierGeneTex
- Product NameWBSCR22 antibody
- Delivery Days Customer9
- Application Supplier NoteWB: 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.
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- CertificationResearch Use Only
- ClonalityPolyclonal
- ConjugateUnconjugated
- Gene ID114049
- Target nameBUD23
- Target descriptionBUD23 rRNA methyltransferase and ribosome maturation factor
- Target synonymsbud 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
- HostRabbit
- IsotypeIgG
- Protein IDO43709
- Protein NameProbable 18S rRNA (guanine-N(7))-methyltransferase
- Scientific DescriptionThis 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
- UNSPSC12352203