NDUFAF1 (NM_016013) Human 3' UTR Clone

Specifications

Product Data
Product Name	NDUFAF1 (NM_016013) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CGI-65; CGI65; CIA30; MC1DN11
ACCN	NM_016013
Insert Size	121 bp
Sequence Data	Insert Sequence (showhide) >SC200736 3’UTR clone of NM_016013 The sequence shown below is from the reference sequence of NM_016013. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCAGAGCTTAACCCAAGGCTTTTTAAATAAAGATCATATGGTAGTTTTGTTTTACTAATCTAAGGGTAC TAGCATCTACAATGATATAGACAAAATAAAATATTTCTTTAATGGCATCCAA 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_016013.4
Synonyms	CGI-65; CGI65; CIA30; MC1DN11
Summary	This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Dec 2011]
Locus ID	51103
MW	4.9

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