Anti-Human /Mouse BUD23 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA02963
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human WBSCR22  
Specificity Strongly expressed in heart, skeletal muscle and kidney. Also expressed in spleen, liver, lung and testis.
Isotype IgG
Reacitivity Human ,Mouse
Clone
Uniprot O43709
Concentration 2.8 mg/mL
Dilution WB 1:200-1:1000, IHC 1:50-100
Formulation
Application WB,ELISA
Other Names HASJ4442,HUSSY 3,HUSSY3,PP3381,Uncharacterized methyltransferase WBSCR22,WBMT,WBS22,WBSCR22,Williams Beuren candidate region putative methyltransferase,Williams Beuren syndrome chromosome region 22 protein,Williams-Beuren syndrome chromosomal region 22 protein
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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