DMGDH (NM_013391) Human 3' UTR Clone

Specifications

Product Data
Product Name	DMGDH (NM_013391) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DMGDHD; ME2GLYDH
ACCN	NM_013391
Insert Size	548 bp
Sequence Data	Insert Sequence (showhide) >SC206697 3’UTR clone of NM_013391 The sequence shown below is from the reference sequence of NM_013391. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGAAAAAAGGTGGAAAGGACAAAACTTGAAAAAAGACCTTCAGCAGTCAACTGAATTAGAGTTGCTAA TGACTGTCCTTGAAATTATTATAACTGGCTCCCAGGGGAATAGAGGAAACCAGGAATTCATTTCAAAAT CATCAAAGTCTAAATTTAGAATCTTAATGAAACCTTTCTGTTAAGTGTTTTCTAAGCAAGACAGAATAA TAGATAAATGATTTACATTGTTCTTTTAAATGAAGAAATTTGAAATGAATGTTTTTTTATTTACCCCAC ATTACCCAATCAGTAAAACATTTAGGTGTTTGCTAATATACACAATCATTACTATAACCTAATTAAGGG ACATTTTATAATTTTAGTAACAAATGCATTCGGTTCTTGACAGCTGAAAACAAATTAATAAATTATCTT TTACATAAAAACATGTACAATATTGTTTATGGATTTACTTCTTTGAGAAATCTTTCCTTAGATGAATAA ATGAAAGTTTTAATTTTTCATGATATATCTGTGATGAAAATAGTAAAACTTAACATTGACATATA 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_013391.3
Synonyms	DMGDHD; ME2GLYDH
Summary	This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
Locus ID	29958
MW	21.1

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