NDUFS6 Protein (Myc-DYKDDDDK Tag)
Quick Overview for NDUFS6 Protein (Myc-DYKDDDDK Tag) (ABIN2727043)
Target
See all NDUFS6 ProteinsProtein Type
Origin
Source
Application
Purity
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Purification tag / Conjugate
- This NDUFS6 protein is labelled with Myc-DYKDDDDK Tag.
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Characteristics
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- Recombinant human NDUFS6 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
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NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6) (AA 1-124) protein (GST tag)
NDUFS6 Origin: Human Host: Wheat germ Recombinant ELISA, WB, AP, AA
NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6) (AA 28-124) protein (His-IF2DI Tag)NDUFS6 Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 90 % as determined by SDS-PAGE. ELISA, WB
NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6) (AA 28-124) protein (His tag)NDUFS6 Origin: Human Host: Escherichia coli (E. coli) Recombinant > 90 % SDS
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Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays -
Comment
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The tag is located at the C-terminal.
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Restrictions
- For Research Use only
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Concentration
- 50 μg/mL
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Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
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Storage
- -80 °C
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Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- NDUFS6 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6))
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Alternative Name
- Ndufs6
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Background
- This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.[provided by RefSeq, Oct 2009].
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Molecular Weight
- 10.8 kDa
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NCBI Accession
- NP_004544
Target
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