DMGDH (NM_013391) Human 3' UTR Clone
CAT#: SC206697
3`UTR clone of dimethylglycine dehydrogenase (DMGDH) nuclear gene encoding mitochondrial protein for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | DMGDH |
Synonyms | DMGDHD; ME2GLYDH |
ACCN | NM_013391 |
Insert Size | 478 |
Sequence Data |
>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. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC AGGTGGAAAGGACAAAACTTGAAAAAAGACCTTCAGCAGTCAACTGAATTAGAGTTGCTAATGACTGTCC TTGAAATTATTATAACTGGCTCCCAGGGGAATAGAGGAAACCAGGAATTCATTTCAAAATCATCAAAGTC TAAATTTAGAATCTTAATGAAACCTTTCTGTTAAGTGTTTTCTAAGCAAGACAGAATAATAGATAAATGA TTTACATTGTTCTTTTAAATGAAGAAATTTGAAATGAATGTTTTTTTATTTACCCCACATTACCCAATCA GTAAAACATTTAGGTGTTTGCTAATATACACAATCATTACTATAACCTAATTAAGGGACATTTTATAATT TTAGTAACAAATGCATTCGGTTCTTGACAGCTGAAAACAAATTAATAAATTATCTTTTACATAAAAACAT GTACAATATTGTTTATGGATTTACTTCTTTGAGAAATCTTTCCTTAGATGAATAAATG ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_013391.2 |
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 |
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