C1orf69 (IBA57) (NM_001010867) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this gene localizes to the mitochondrion and is part of the iron-sulfur cluster assembly pathway. The encoded protein functions late in the biosynthesis of mitochondrial 4Fe-4S proteins. Defects in this gene have been associated with autosomal recessive spastic paraplegia-74 and with multiple mitochondrial dysfunctions syndrome-3. Two transcript variants encoding different isoforms have been found for this gene. The smaller isoform is not likely to be localized to the mitochondrion since it lacks the amino-terminal transit peptide. [provided by RefSeq, Jul 2015]
Synonyms
C1orf69; MMDS3; SPG74
Gene ID
200205
UniProt
Q5T440
Accession Number mRNA
NM_001010867
Chromosomal Location
1q42.13
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
38 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
IBA57
Species
Human
Protein ID
NP_001010867
Overview
Recombinant protein of human chromosome 1 open reading frame 69 (C1orf69)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/200205
Uniprot URL
https://www.uniprot.org/uniprot/Q5T440
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_001010867
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_001010867
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