NDUFS6 Protein (Myc-DYKDDDDK Tag)
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- Target Alle NDUFS6 Proteine anzeigen
- NDUFS6 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6))
- Protein-Typ
- Recombinant
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Spezies
- Human
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Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses NDUFS6 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human NDUFS6 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product NDUFS6 Protein
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- Applikationshinweise
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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 - Kommentare
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The tag is located at the C-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Lagerung
- -80 °C
- Informationen zur Lagerung
- 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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- Target
- NDUFS6 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6))
- Andere Bezeichnung
- Ndufs6 (NDUFS6 Produkte)
- Synonyme
- BC059730 Protein, IP13 Protein, Ip13dis Protein, Ndub13 Protein, RATIp13dis Protein, CI-13kA Protein, CI-13kD-A Protein, CI13KDA Protein, NADH dehydrogenase (ubiquinone) Fe-S protein 6 Protein, NADH:ubiquinone oxidoreductase subunit S6 Protein, Ndufs6 Protein, NDUFS6 Protein
- Hintergrund
- 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].
- Molekulargewicht
- 10.8 kDa
- NCBI Accession
- NP_004544
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