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SPART (NM_001142295) Human Recombinant Protein

Selected Variant

PH33326M5

Size: 20 µg

Product Specifications

Background

This gene encodes a protein containing a MIT (Microtubule Interacting and Trafficking molecule) domain, and is implicated in regulating endosomal trafficking and mitochondria function. The protein localizes to mitochondria and partially co-localizes with microtubules. Stimulation with epidermal growth factor (EGF) results in protein translocation to the plasma membrane, and the protein functions in the degradation and intracellular trafficking of EGF receptor. Multiple alternatively spliced variants, encoding the same protein, have been identified. Mutations associated with this gene cause autosomal recessive spastic paraplegia 20 (Troyer syndrome) . [provided by RefSeq, Nov 2008]

Overview

Purified recombinant protein of Homo sapiens spastic paraplegia 20 (Troyer syndrome) (SPG20), transcript variant 3

Synonyms

SPG20; TAHCCP1

Gene ID

23111

UniProt

Q8N0X7, A0A024RDV9

Accession Number mRNA

NM_001142295

Chromosomal Location

13q13.3

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

72.7 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

SPART

Species

Human

Protein ID

NP_001135767

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/23111

Uniprot URL

https://www.uniprot.org/uniprot/Q8N0X7

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_001142295

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_001135767

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