NDUFA10 (NM_004544) Human Untagged Clone

SKU SC322210

NDUFA10 (untagged)-Human NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 10, 42kDa (NDUFA10), nuclear gene encoding mitochondrial protein

Product Data

• Type: Human Untagged Clone
• Target Symbol: NDUFA10
• Synonyms: CI-42k; CI-42KD; MC1DN22
• Vector: pCMV6-AC
• E. coli Selection: Ampicillin (100 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >OriGene sequence for SC322210 CCTTGGGTCCTTGATCCTGAGCTGACCGGGTAGCCATGGCCTTGCGGCTCCTGAAGCTGG; CAGCGACGTCCGCGTCCGCCCGGGTCGTGGCGGCGGGCGCCCAGCGCGTGAGAGGAATTC; ATAGCAGTGTGCAGTGCAAGCTGCGCTATGGAATGTGGCATTTCCTACTTGGGGATAAAG; CAAGCAAAAGACTGACAGAACGCAGCAGAGTGATAACTGTAGATGGCAATATATGTACTG; GAAAAGGCAAACTTGCAAAAGAAATAGCAGAGAAACTAGGCTTCAAGCACTTTCCTGAAG; CGGGGATTCATTATCCAGACAGTACCACAGGAGATGGGAAGCCCCTCGCCACCGACTATA; ATGGCAACTGTAGTTTGGAGAAATTTTACGATGATCCGAGAAGCAATGATGGCAACAGTT; ACCGCCTGCAGTCCTGGTTGTACAGCAGTCGCCTGCTGCAGTACTCAGATGCCTTGGAGC; ACTTGCTGACCACAGGACAAGGTGTTGTGTTGGAGCGCTCCATCTTCAGTGACTTTGTGT; TCCTGGAGGCGATGTACAACCAGGGATTCATCCGAAAGCAGTGTGTGGACCACTACAACG; AGGTGAAGAGCGTCACCATCTGCGATTACCTGCCCCCCCACCTGGTGATTTACATCGATG; TGCCCGTTCCAGAGGTCCAGAGGCGGATTCAGAAGAAAGGAGATCCACATGAAATGAAGA; TCACCTCTGCCTATCTACAGGACATTGAGAATGCCTATAAGAAAACCTTTCTCCCTGAGA; TGAGTGAAAAATGTGAGGTTTTACAGTATTCTGCAAGGGAAGCTCAAGATTCAAAAAAGG; TGGTAGAGGACATTGAATACCTGAAGTTCGATAAAGGGCCGTGGCTCAAGCAGGACAATC; GCACTTTATACCACCTGCGATTACTGGTTCAGGATAAGTTTGAGGTGCTGAATTACACAA; GCATTCCTATCTTTCTCCCGGAAGTCACCATTGGAGCTCATCAGACTGACCGTGTCTTAC; ATCAGTTCAGAGAGCTGCCGGGCCGCAAGTACAGCCCTGGGTACAACACCGAGGTGGGAG; ACAAGTGGATCTGGCTGAAGTGAACGGGCCGCCTTCTGCTCCAGCTGCATCACAGTGATG; GCCAAGCTGCATCAGCCGCACTCTCCTGGACGCCATATAGCTTTAAGATCGGGGGAGGGT; AAATAATGCAAAAATTGCACAGTGGAAGAAGGGGTCTCACAAAAAGCAATCCATCCTGTA; GTATAGGTAATGGAGTTGGGGGAAGCAGCTTCCATTCTGGATGTTTGGAACCCTTTAGCT; TTGTTTTGGAATGGCCCACCATTCTCACTGGAAAACAGTGGTCTGCTGTGAAAGGCCAGC; TCTCGGCAGCCCCTGTGGTTTCAGCGCTGCCGCTCTGTGTCATTCAGGTTGTGCACATTG; TTTTTCTTCTGACTTCCAGAAATAAAAGTGTTTCCATGGGAAAAAAAAAAAAAAAAAAAA; AAAAAAAAAAAA
• Restriction Sites: Please inquire
• ACCN: NM_004544
• OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
• OTI Annotation: This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.
• Components: The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
• Reconstitution Method: 1. Centrifuge at 5,000xg for 5min.; 2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.; 3. Close the tube and incubate for 10 minutes at room temperature.; 4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.; 5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
• Note: Plasmids are not sterile. For experiments where strict sterility is required, filtration with 0.22um filter is required.
• Shipping: Ambient

Reference Data

• RefSeq: NM_004544.2, NP_004535.1
• RefSeq Size: 1557 bp
• RefSeq ORF: 1068 bp
• Locus ID: 4705
• UniProt ID: O95299
• Cytogenetics: 2q37.3
• Domains: dNK
• Protein Pathways: Alzheimer's disease, Huntington's disease, Metabolic pathways, Oxidative phosphorylation, Parkinson's disease
• Summary: The protein encoded by this gene is a component of 42 kDa complex I, the first enzyme complex in the electron transport chain of mitochondria. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. A mutation in this gene was found in an individual with Leigh syndrome. [provided by RefSeq, Apr 2016]