Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody

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Catalogue No: abx031474
Price: US$326.25
(Size: 80 µl)

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Documents

Datasheet SDS
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.

Target Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22)
Clonality Polyclonal
Reactivity Human
Tested Applications ELISA, WB
Host Rabbit
Recommended dilutions WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 253-281 amino acids from the C-terminal region of human WBSCR22.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC O43709 (UniProt, ExPASy)
UniProt Secondary AC A8K501, C9K060, Q96P12, Q9BQ58, Q9HBP9
UniProt Entry Name BUD23_HUMAN
Gene Symbol BUD23
KEGG hsa:114049
String 9606.ENSP00000401191
Molecular Weight Calculated MW: 31.9 kDa
Buffer PBS containing 0.09% sodium azide.
Specificity Predicted to react with Mouse and Cow BUD23.
Availability Shipped within 5-10 working days.
Note THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.
Research Articles on Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22)


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