WBSCR22 Blocking Peptide (C-term)
€363.00
In stock
SKU
AC-BP20254b
Background:
This gene encodes a protein containing a nuclearlocalization signal and an S-adenosyl-L-methionine binding motiftypical of methyltransferases, suggesting that the encoded proteinmay act on DNA methylation. This gene is deleted in Williamssyndrome, a multisystem developmental disorder caused by thedeletion of contiguous genes at 7q11.23.
Other Names:
Probable 18S rRNA (guanine-N(7))-methyltransferase, 211-, Bud site selection protein 23 homolog, Metastasis-related methyltransferase 1, Williams-Beuren syndrome chromosomal region 22 protein, WBSCR22, MERM1
Target/Specificity:
The synthetic peptide sequence is selected from aa 268-281 of HUMAN WBSCR22
Gene Name: BUD23 (HGNC:16405)
Gene ID: 114049
Primary Accession: O43709
Other Accession: Q9CY21; Q58DP0; NP_059998.2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a protein containing a nuclearlocalization signal and an S-adenosyl-L-methionine binding motiftypical of methyltransferases, suggesting that the encoded proteinmay act on DNA methylation. This gene is deleted in Williamssyndrome, a multisystem developmental disorder caused by thedeletion of contiguous genes at 7q11.23.
Other Names:
Probable 18S rRNA (guanine-N(7))-methyltransferase, 211-, Bud site selection protein 23 homolog, Metastasis-related methyltransferase 1, Williams-Beuren syndrome chromosomal region 22 protein, WBSCR22, MERM1
Target/Specificity:
The synthetic peptide sequence is selected from aa 268-281 of HUMAN WBSCR22
Gene Name: BUD23 (HGNC:16405)
Gene ID: 114049
Primary Accession: O43709
Other Accession: Q9CY21; Q58DP0; NP_059998.2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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