WRN (NM_000553) Human 3' UTR Clone
CAT#: SC208817
3' UTR clone of Werner syndrome RecQ helicase-like (WRN) 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 | WRN (NM_000553) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | RECQ3; RECQL2; RECQL3 |
ACCN | NM_000553 |
Insert Size | 2000 bp |
Sequence Data |
>SC208817 3’UTR clone of NM_000553
The sequence shown below is from the reference sequence of NM_000553. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAAACGAAAAGGGGAGGTCTTTTTAGTTAAGCTGGCAATTACCAGAACAATTATGTTTCTTGCTGTATT ATAAGAGGATAGCTATATTTTATTTCTGAAGAGTAAGGAGTAGTATTTTGGCTTAAAAATCATTCTAAT TACAAAGTTCACTGTTTATTGAAGAACTGGCATCTTAAATCAGCCTTCCGCAATTCATGTAGTTTCTGG GTCTTCTGGGAGCCTACGTGAGTACATCACCTAACAGAATATTAAATTAGACTTCCTGTAAGATTGCTT TAAGAAACTGTTACTGTCCTGTTTTCTAATCTCTTTATTAAAACAGTGTATTTGGAAAATGTTATGTGC TCTGATTTGATATAGATAACAGATTAGTAGTTACATGGTAATTATGTGATATAAAATATTCATATATTA TCAAAATTCTGTTTTGTAAATGTAAGAAAGCATAGTTATTTTACAAATTGTTTTTACTGTCTTTTGAAG AAGTTCTTAAATACGTTGTTAAATGGTATTAGTTGACCAGGGCAGTGAAAATGAAACCGCATTTTGGGT GCCATTAAATAGGGAAAAAACATGTAAAAAATGTAAAATGGAGACCAATTGCACTAGGCAAGTGTATAT TTTGTATTTTATATACAATTTCTATTATTTTTCAAGTAATAAAACAATGTTTTTCATACTGAATATTAT ATATATATTTTTTAGCTTTCATTTACTTAATTATTTTAAGTACCTTTATTTTTCCAGGATGTCAGAATT TGATTCTAATCTCTCTTATGTAGCACATGTGACTTAATTTAAAACCTATACTGTGACACAGAGTTGGGT AAACGATGATTATTTAACTTTAAGCAGTTCACCATCCATTTCAAAGCCTTTGATTGGCTTTTTTGTAAA TAAAAATAACTTGTTAAGAAACAAATATATCTGTCATAGAAGAACTAGAAAATCCAGGGAAGTGAGAAA AATGAAAATAAAAATCATTCATAGTTTTACTAGTAGCTAATCACAGTCAACCTCTTTTGTGTATCCCAC CAGACTTTTTTATATTCATTTGTTTTTAGTTAAAATATAAAAGTCTCGTATATTCCCATTTTTCTGCAT TGCATTACCAGAAGGTAGTGGCGCCTATTAAATATGTGATATGTTGTTGTCCAGCCATGGCTTCTGCAT TTGCATGCTTTTGTGTGTGCATCTGCAATACCCTGTGAATATCCTGTGTGATGGAGTGGCAAGTACGCA CAGACACGTCTGCTGCATGCCTAGGTACGAGGCTGTCTCCAGGAGAAGCACTTGTTTGATTATTTGAGT TGCCAATTGAATTTGCTGCTTTTTTTCATGGCTTGCCATTTTCACTGAAAAGAATGACTAATGAAAAAC GATGATTGGTTATTAGATTTGGATGTTTGGCAGACATTTTCTCAAAATTGAACTAAGTTGGCCTCTTCA CGGAAAACAACTGGTATTTGTTGTGCCAATGATAAAATTGGAGATTTCTAGCAAAATGTATAATTTTGG AAAAGTTGTGTTCCTCCACTGGAAGCTTGACAGCTTTCCTTAACATAAAGACTTCTCTTTCTCTTCGCT TTCACTACTACTACTACTAATTCTTCTTCTGATTCTTCTTCTTCTCCTTCTTCCTTCTTCCTTCCTTCC TCCTCCTCCTCCTTCTTCTTCCTCTTCCTCTTCTTCTTTCTCTCTTTCCTTCCTTCCCTTCCCTTCCCC TTCCTTCCTTCCTTCCTTCCTTCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCTTTCTTTTTCTTTC TCTTTCTTTCTTTCTTTCTCTCTCTCTCTCTCTTTCTTTCTTTTTCTTTCTCTTTTTCTTTCTTTCAAG CAGTCCTCCCGCCTCAGTCCCCCAAAATAGTGGGATTACAGGTGTGAGCCACCATGCACAGCCTTACAT AAAGCCTTTTCTAATGAGATGGATAGTAATTAACAAATGTGAGTTTTTGATATTATATAAAGATTTTT 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_000553.6 |
Synonyms | RECQ3; RECQL2; RECQL3 |
Summary | This gene encodes a member of the RecQ subfamily of DNA helicase proteins. The encoded nuclear protein is important in the maintenance of genome stability and plays a role in DNA repair, replication, transcription and telomere maintenance. This protein contains a N-terminal 3' to 5' exonuclease domain, an ATP-dependent helicase domain and RQC (RecQ helicase conserved region) domain in its central region, and a C-terminal HRDC (helicase RNase D C-terminal) domain and nuclear localization signal. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by accelerated aging and an elevated risk for certain cancers. [provided by RefSeq, Aug 2017] |
Locus ID | 7486 |
MW | 78.1 |
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