TRMT1 (TRMU) (NM_018006) Human 3' UTR Clone
CAT#: SC204596
3' UTR clone of tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase (TRMU) nuclear gene encoding mitochondrial protein transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | TRMT1 (TRMU) (NM_018006) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | LCAL3; MTO2; MTU1; TRMT; TRMT1 |
ACCN | NM_018006 |
Insert Size | 364 bp |
Sequence Data |
>SC204596 3’UTR clone of NM_018006
The sequence shown below is from the reference sequence of NM_018006. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GATGGTCCAGGCCTGAGTCCCTTGCTCTGACAGAGATGGATCTGCTAGAAGGAACCTGGAGAGCAGGAC CCATGGCTGGGCGGCTGGTGAGCAGTCCAGGTGCCCAAGGGCCAGCTTGCTGCTGCCCAAAGCAGAGGA AGCCGGGCTGGCTGAGGGTCCGAAAAGCCTGCAGGGGCCCGGCGAGCCCCAGGAAGAGCCTCAGCTCCA GGCTGGGGCTCTGGCTGCTGGAGCATCTGCTGGCTGGTGGGGTGGCCCGAGTTCCCCTTCACCGCCCCC AGGGAGGGTTTCCCACCTCAGAGTACACCGAGGGGACCTGCAGAGGGGGCTGTCGGGACAGCGTGGAAT AAACATTATTTCAAGGACA 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_018006.5 |
Synonyms | LCAL3; MTO2; MTU1; TRMT; TRMT1 |
Summary | This nuclear gene encodes a mitochondrial tRNA-modifying enzyme. The encoded protein catalyzes the 2-thiolation of uridine on the wobble positions of tRNA(Lys), tRNA(Glu), and tRNA(Gln), resulting in the formation of 5-taurinomethyl-2-thiouridine moieties. Mutations in this gene may cause transient infantile liver failure. Polymorphisms in this gene may also influence the severity of deafness caused by mitochondrial 12S ribosomal RNA mutations. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
Locus ID | 55687 |
MW | 12.9 |
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