WBSCR22 293T Cell Transient Overexpression Lysate(Denatured)
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More Files
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Specification
Transfected Cell Line
293T
Plasmid
pCMV-WBSCR22 full-length
Host
Human
Theoretical MW (kDa)
31.9
Interspecies Antigen Sequence
Mouse (79); Rat (79)
Quality Control Testing
Transient overexpression cell lysate was tested with Anti-WBSCR22 antibody (H00114049-B01) by Western Blots.
SDS-PAGE Gel
WBSCR22 transfected lysate.
Western Blot
Lane 1: WBSCR22 transfected lysate ( 31.9 KDa)
Lane 2: Non-transfected lysate.Storage Buffer
1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Storage Instruction
Store at -80°C. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot
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Gene Info — WBSCR22
Entrez GeneID
114049GeneBank Accession#
NM_017528.2Protein Accession#
NP_059998.2Gene Name
WBSCR22
Gene Alias
HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
Gene Description
Williams Beuren syndrome chromosome region 22
Gene Ontology
HyperlinkGene Summary
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. [provided by RefSeq
Other Designations
Williams Beuren syndrome chromosome region 22 protein|Williams-Beuren candidate region putative methyltransferase
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Interactome
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Pathway
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