NDUFS2 (NM_001166159) Human 3' UTR Clone

Specifications

Product Data
Product Name	NDUFS2 (NM_001166159) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CI-49; MC1DN6
ACCN	NM_001166159
Insert Size	484 bp
Sequence Data	Insert Sequence (showhide) >SC206362 3’UTR clone of NM_001166159 The sequence shown below is from the reference sequence of NM_001166159. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCCATCATAGGTACGAGGCCTATTGTGTAGTAGAGGTATCCTAGACAAAGGAGTTCGGGACGCCCACTG GGGACAGAAGGAGAACACTTCCTGTTCACCATAGGCCATGGCATGGACTCGGGTCCTCAATCTTTTGAG CACAGTAATGGGTTCTGGATCTTGGGTAACACCACTTTTTTTGTTTGTTTTGCCTCACAACAGGAAGAT AAGTAACATCACTTTTTTCCTCCATCCTCTCACCTAGGTACCCAAGATATTGTATTTGGAGAAGTAGAT CGGTGAGCAGGGGAGCAGCGTTTGATCCCCCCTGCCTATCAGCTTCTTCTGTGGAGCCTGTTCCTCACT GGAAATTGGCCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTTCATGTACACTTGGCTGTCAG GCTTTCTGTGCATGTACTAAAAAAGGAGAAATTATAATAAATTAGCCGTCTTGCGGCCCCTAGGCCTAAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_001166159.2
Synonyms	CI-49; MC1DN6
Summary	The protein encoded by this gene is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I). Mammalian mitochondrial complex I is composed of at least 43 different subunits, 7 of which are encoded by the mitochondrial genome, and the rest are the products of nuclear genes. The iron-sulfur protein fraction of complex I is made up of 7 subunits, including this gene product. Complex I catalyzes the NADH oxidation with concomitant ubiquinone reduction and proton ejection out of the mitochondria. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]
Locus ID	4720
MW	17.6

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