TOM1L2 (NM_001082968) Human Recombinant Protein
Product Specifications
Background
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. [provided by RefSeq, Apr 2017]
Overview
Recombinant protein of human target of myb1-like 2 (chicken) (TOM1L2), transcript variant 3
Synonyms
FLJ21501; FLJ32746
Gene ID
146691
UniProt
Q6ZVM7
Accession Number mRNA
NM_001082968
Chromosomal Location
17p11.2
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Molecular Weight
55.4 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
TOM1L2
Species
Human
Protein ID
NP_001076437
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/146691
Uniprot URL
https://www.uniprot.org/uniprot/Q6ZVM7
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001082968
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001076437
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