ETHE1 (NM_014297) Human Recombinant Protein
Product Specifications
Background
This gene encodes a member of the metallo beta-lactamase family of iron-containing proteins involved in the mitochondrial sulfide oxidation pathway. The encoded protein catalyzes the oxidation of a persulfide substrate to sulfite. Certain mutations in this gene cause ethylmalonic encephalopathy, an infantile metabolic disorder affecting the brain, gastrointestinal tract and peripheral vessels. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2016]
Overview
Recombinant protein of human ethylmalonic encephalopathy 1 (ETHE1)
Synonyms
HSCO; YF13H12
Gene ID
23474
UniProt
O95571, A0A0S2Z5B3
Accession Number mRNA
NM_014297
Chromosomal Location
19q13.31
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
27.7 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
ETHE1
Species
Human
Protein ID
NP_055112
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/23474
Uniprot URL
https://www.uniprot.org/uniprot/O95571
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_014297
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_055112
Frequently Asked Questions
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