SPART (NM_001142296) Human Recombinant Protein
Selected Variant
PH33325M5
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 2
Synonyms
SPG20; TAHCCP1
Gene ID
23111
UniProt
Q8N0X7, A0A024RDV9
Accession Number mRNA
NM_001142296
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_001135768
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_001142296
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001135768
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