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FIGURE: 1 / 4
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total TOM1L2.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: FLJ32746; myb1-like protein 2; target of Myb-like protein 2; target of myb1-like 2; TOM1L2; similar to Gallus gallus TOM1; unnamed protein product; UNQ3124
Gene Aliases: 2900016I08Rik; A730055F12Rik; Srebf1
UniProt ID: (Human) Q6ZVM7, (Mouse) Q5SRX1
Entrez Gene ID: (Human) 146691, (Rat) 360537, (Mouse) 216810
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