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C1orf69 (IBA57) (NM_001010867) Human Recombinant Protein

Selected Variant

PH36756M5

Size: 20 µg

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]

Overview

Recombinant protein of human chromosome 1 open reading frame 69 (C1orf69)

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

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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