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

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Catalogue No: abx005524
Price: US$217.50
(Size: 20 µl)

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Datasheet SDS
WBSCR22 Antibody is a Rabbit Polyclonal antibody against WBSCR22. 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.

Target Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22)
Clonality Polyclonal
Reactivity Human, Rat
Tested Applications ELISA, WB, IF/ICC
Host Rabbit
Recommended dilutions ELISA: 1 µg/ml, WB: 1/500 - 1/2000, IF/ICC: 1/50 - 1/100. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1-281 of human WBSCR22.
Isotype IgG
Form Liquid
Purification Purified by affinity chromatography.
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
GeneID 114049
NCBI Accession NP_059998.2
KEGG hsa:114049
String 9606.ENSP00000401191
Molecular Weight Calculated MW: 32 kDa
Observed MW: 36 kDa
Buffer PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Concentration > 0.2 mg/ml
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22)


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