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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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