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Description
This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq
Specifications
Specifications
| Antigen | WBSCR27 |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 2A12 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full-length recombinant WBSCR27. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | WBSCR27 |
| Gene Accession No. | BC030295.2 |
| Gene Alias | MGC40131 |
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