PEAMT (PEMT) (NM_148173) Human 3' UTR Clone
CAT#: SC202867
3' UTR clone of phosphatidylethanolamine N-methyltransferase (PEMT) nuclear gene encoding mitochondrial protein transcript variant 3 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 | PEAMT (PEMT) (NM_148173) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | PEAMT; PEMPT; PEMT2; PLMT; PNMT |
ACCN | NM_148173 |
Insert Size | 258 bp |
Sequence Data |
>SC202867 3’UTR clone of NM_148173
The sequence shown below is from the reference sequence of NM_148173. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAAGCCTCCGGGTCCCACAAGAGGAGCTGATTGAGCTGCAACAGCTTTGCTGAAGGCCTGGCCAGCCTC CTGGCCTGCCCCAAGTGGCAGGCCCTGCGCAGGGCGAGAATGGTGCCTGCTGCTCAGGGCTCGCCCCCG GCGTGGGCTGCCCCAGTGCCTTGGAACCTGCTGCCTTGGGGACCCTGGACGTGCCGACATATGGCCATT GAGCTCCAACCCACACATTCCCATTCACCAATAAAGGCACCCTGACCCCAA 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_148173.2 |
Synonyms | PEAMT; PEMPT; PEMT2; PLMT; PNMT |
Summary | Phosphatidylcholine (PC) is the most abundant mammalian phospholipid. This gene encodes an enzyme which converts phosphatidylethanolamine to phosphatidylcholine by sequential methylation in the liver. Another distinct synthetic pathway in nucleated cells converts intracellular choline to phosphatidylcholine by a three-step process. The protein isoforms encoded by this gene localize to the endoplasmic reticulum and mitochondria-associated membranes. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2012] |
Locus ID | 10400 |
MW | 9.4 |
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