Analytical Data
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Gene name
COQ6
- Application
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Alternative Names
COQ6；Ubiquinone biosynthesis monooxygenase COQ6. mitochondrial
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Species
Human
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Source
E. coli
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Tag
His tag N-Terminus
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Purity
Greater than 90% as determined by SDS-PAGE.
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Uniprot
Q9Y2Z9
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Expression Region
1-468aa
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AA Sequence
MAARLVSRCG AVRAAPHSGP LVSWRRWSGA STDTVYDVVV SGGGLVGAAM ACALGYDIHF HDKKILLLEA GPKKVLEKLS ETYSNRVSSI SPGSATLLSS FGAWDHICNM RYRAFRRMQV WDACSEALIM FDKDNLDDMG YIVENDVIMH ALTKQLEAVS DRVTVLYRSK AIRYTWPCPF PMADSSPWVH ITLGDGSTFQ TKLLIGADGH NSGVRQAVGI QNVSWNYDQS AVVATLHLSE ATENNVAWQR FLPSGPIALL PLSDTLSSLV WSTSHEHAAE LVSMDEEKFV DAVNSAFWSD ADHTDFIDTA GAMLQYAVSL LKPTKVSARQ LPPSVARVDA KSRVLFPLGL GHAAEYVRPR VALIGDAAHR VHPLAGQGVN MGFGDISSLA HHLSTAAFNG KDLGSVSHLT GYETERQRHN TALLAATDLL KRLYSTSASP LVLLRTWGLQ ATNAVSPLKE QIMAFASK
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Endotoxin
< 1.0 EU per μg protein as determined by the LAL method.
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Form
Freeze-dried powder
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Buffer formulation
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
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Reconstitution
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- Customization
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Stability Test
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
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Storage & Shelf Life
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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Shipping
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
COQ6, a key enzyme in the coenzyme Q (CoQ) biosynthetic pathway, has garnered significant interest in recent years due to its vital role in mitochondrial function and cellular energy production. Coenzyme Q, also known as ubiquinone, is essential for the electron transport chain, contributing to ATP synthesis and acting as an antioxidant. Deficiencies in CoQ can lead to a range of mitochondrial disorders, which often manifest as neurodegenerative diseases or muscle weakness. Research on COQ6 recombinant protein has focused on understanding its catalytic mechanism and structural properties, as well as its interactions with other proteins in the biosynthetic pathway. Understanding the functionality of COQ6 can provide insights into the molecular basis of CoQ deficiencies and their associated diseases. Furthermore, recombinant COQ6 can potentially serve as a valuable tool for the development of therapeutic strategies aimed at restoring CoQ levels in affected individuals. This area of study continues to evolve, with ongoing efforts to characterize COQ6's biological activity, enhance its expression systems, and explore its potential applications in both basic research and clinical settings. Overall, COQ6 represents a promising target for interventions aimed at ameliorating mitochondrial dysfunction and improving patient outcomes in related disorders.
