NDUFS4 (NM_002495) Human 3' UTR Clone

Specifications

Product Data
Product Name	NDUFS4 (NM_002495) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AQDQ; CI-18; CI-18 kDa; CI-AQDQ; MC1DN1
ACCN	NM_002495
Insert Size	147 bp
Sequence Data	Insert Sequence (showhide) >SC200918 3’UTR clone of NM_002495 The sequence shown below is from the reference sequence of NM_002495. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AACAAAAGAACAAGAGTATCCACAAAATAGGTTGGCACTGACTATATCTCTGCTTGACTGTGAATAAAG TCAGCTGTGCAGTATTTATAGTCCATGTATAATAAATACATCTCTTAATCTCCTAATAAATTGGACCTT TAAACTACA 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_002495.4
Synonyms	AQDQ; CI-18; CI-18 kDa; CI-AQDQ; MC1DN1
Summary	This gene encodes an nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I, or NADH:ubiquinone oxidoreductase). Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Locus ID	4724
MW	5.6

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