TMEM126A (NM_032273) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7) . Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
Overview
Recombinant protein of human transmembrane protein 126A (TMEM126A)
Synonyms
OPA7
Gene ID
84233
UniProt
Q9H061
Accession Number mRNA
NM_032273
Chromosomal Location
11q14.1
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
Function
Transmembrane
Molecular Weight
21.3 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
TMEM126A
Species
Human
Protein ID
NP_115649
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/84233
Uniprot URL
https://www.uniprot.org/uniprot/Q9H061
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_032273
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_115649
Frequently Asked Questions
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