WBSCR27 Antibody (N-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP10548a
Background:
WBSCR27 encodes a protein belonging to ubiE/COQ5methyltransferase family. The gene is deleted in Williams syndrome,a multisystem developmental disorder caused by the deletion ofcontiguous genes at 7q11.22-q11.23.
Other Names:
Williams-Beuren syndrome chromosomal region 27 protein, WBSCR27
Gene Name: METTL27 (HGNC:19068)
Gene ID: 155368
Primary Accession: Q8N6F8
Other Accession: NP_689772.2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
WBSCR27 encodes a protein belonging to ubiE/COQ5methyltransferase family. The gene is deleted in Williams syndrome,a multisystem developmental disorder caused by the deletion ofcontiguous genes at 7q11.22-q11.23.
Other Names:
Williams-Beuren syndrome chromosomal region 27 protein, WBSCR27
Gene Name: METTL27 (HGNC:19068)
Gene ID: 155368
Primary Accession: Q8N6F8
Other Accession: NP_689772.2
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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