TOM1L2 Polyclonal Antibody, Invitrogen™

Descripción

Immunogen sequence: LLHVNDDLNN VFLRYERFER YRSGRSVQNA SNGVLNEVTE DNLIDLGPGS PAVVSPMVGN TAPPSSLSSQ LAGLDLGTES VSGTLSSLQQ CNPRDGF Highest antigen sequence identity to the following orthologs: Mouse - 96%, Rat - 96%.

This gene belongs to a small gene family whose members have an N-terminal VHS domain followed by a GAT domain; domains which typically participate in vesicular trafficking. The canonical protein encoded by this gene also has a C-terminal clathrin binding motif. This protein has been shown to interact with Tollip, clathrin and ubiquitin and is thought to play a role in endosomal sorting. This gene resides in the 3.7 Mb deletion of chromosome region 17p11.2 that is associated with Smith-Magenis syndrome. Alternative splicing results in multiple transcript variants encoding distinct proteins.