Twinkle (TWNK) (NM_021830) Human 3' UTR Clone
CAT#: SC211019
3' UTR clone of chromosome 10 open reading frame 2 (C10orf2) 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 | Twinkle (TWNK) (NM_021830) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | ATXN8; C10orf2; IOSCA; MTDPS7; PEO; PEO1; PEOA3; PRLTS5; SANDO; SCA8; TWINL |
ACCN | NM_021830 |
Insert Size | 923 bp |
Sequence Data |
>SC211019 3’UTR clone of NM_021830
The sequence shown below is from the reference sequence of NM_021830. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGCCAGACACCTCCAAGCGTTCAAAGTGAAGGCCGTGCAGAGCTGGTCACTGAAATGAGCCTGATAGG ATAGGCTGGAGCATAAAACTCTGCAAGGGCTCCTCTATCCTGTGGTCCTGAGCTGTGTGCCCTTCTCAG TCTGAGGGGCCTAACCTAGAGCAGGTTTCCATAGTGAGAAAATTCAATGTAGCAGACTACTGAGAAACT ACTGTGTTGCTCAGGCTTTGTTTGAGGTCCTGTATATACAGCACTGAAAAGAGAGATAAAGTCCCTGCC TGCATGCATTCTGGCGGAAGAGACAAGCAAGCAATGAACAAATTAGCAGAAAACCTAGTTTTAGTGAAA AATGCTGTAAAGAAAATAGAAATGCGATAGAGTGCTGGCAGGCTAGTGTAGATAAGTGGTCTGAAAAGG TGTCTCTGAGCCGAGGGCATGTGAGCTGGGGCCTAAACAACTAGAAGGAGAGAGCCACGTGAACATCCG GCGAAGGGGACCCAGGCAGAGAGAAAAGGAAATCCAAGCCCTGAGGTAGGAATGAGCAGGTCAGATTCA AGGCAGTGAGGTCAGGCCGCATGAACCTGGAGGGGAATCGGGGACTTCATGCGAAACTCCAGCCTAGGC TTTCAAAGTCAAAGGGTGATACAGTGGGTACCAAGCTCCTCTGCTCCCCACTTTGTAGAGCCTAGCATG AGGTGGCATGTACTAGAATTGGATCCTAGGTGCTTAGCCCTGCAATATCAGGGCCTCACTGGTGGGAGC TGCCTCGGGCTGGGTTGCTTGGTCATAGAGCCATAGAAGGAAGCTGTCAGCCCGGAGTGCCTGCCACCT AGACACTGATGCCATTGTGTGCTGCCTCAAGACTGCTGGAGTCAGGACATTTTATAGAGCCTTTTCCAG TTTTACTAAAAAATTTTTCCATTGCC 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_021830.5 |
Synonyms | ATXN8; C10orf2; IOSCA; MTDPS7; PEO; PEO1; PEOA3; PRLTS5; SANDO; SCA8; TWINL |
Summary | This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009] |
Locus ID | 56652 |
MW | 34.3 |
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