NDUFV1 (NM_007103) Human 3' UTR Clone

Specifications

Product Data
Product Name	NDUFV1 (NM_007103) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CI-51K; CI51KD; MC1DN4; UQOR1
ACCN	NM_007103
Insert Size	126 bp
Sequence Data	Insert Sequence (showhide) >SC200397 3’UTR clone of NM_007103 The sequence shown below is from the reference sequence of NM_007103. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCATCAGGCCCGGCAGGCTGCCTCTTAGCCCACCACCCTGGCCTGCTGTCCTGCGTCTATCCATGTG GAATGCTGGACAATAAAGCGAGTGCTGCCCACCCTCCAGCTGCCGCTGCTGTGACTG 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_007103.4
Synonyms	CI-51K; CI51KD; MC1DN4; UQOR1
Summary	The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]
Locus ID	4723
MW	4.6

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