Search results for Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody
Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody, Abbexa, abx031474
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.
Host
Rabbit
Reactivity
Human
Applications
ELISA, WB
Conjugation
Unconjugated
Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody, Abbexa, abx005524
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.
Host
Rabbit
Reactivity
Human, Rat
Applications
ELISA, WB, IF/ICC
Conjugation
Unconjugated
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