Probable hydrolase PNKD (PNKD) (NM_015488) Human 3' UTR Clone
CAT#: SC216651
3' UTR clone of paroxysmal nonkinesigenic dyskinesia (PNKD) transcript variant 1 for miRNA target validation
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CNY 5,795.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | Probable hydrolase PNKD (PNKD) (NM_015488) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BRP17; DYT8; FKSG19; FPD1; KIPP1184; MR-1; MR-1S; MR1; PDC; PKND1; PNKD1; R1; TAHCCP2 |
ACCN | NM_015488 |
Insert Size | 1842 bp |
Sequence Data |
>SC216651 3’UTR clone of NM_015488
The sequence shown below is from the reference sequence of NM_015488. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGGCTGAAGGATATGCACAAGAGCAAGTGATGCCCCCAGCGCCCCCAGCCCAGCCCACTCCCCGCATGG GGAGGCCGCCACCACCAACACCTCATCATCCTTCTCATCGCTAACACCACCACCTCCATCGGCACCCAA GCGGGCATCATCCCCCCACACTGCTCAGGGGAGGGGAGGGATCAGGCGATGAGACTGTGAGGCCAAAAG AAGGGGGCCTGTTGGAGGCTGGGAACCCCGCAGCGCGAGGCTGCCTCATCAACGGCAAGAGGAAAGGAG GGGTCTCGGGACATCTCCAGACCCTACCAACTGGGAGGGTCCCCTCCTCCTTCCCTACTCCTGGGACGG CAGCAAGGACATGGGGGCTGCTGTTAGCTTCTCCGTCAGGAGGCCTCATCTCACTGTAGCCCTGGAACC CAGGGTCCATCTTGCCCTTCCCCCATCCATGGTTGGGAAAGAAGCTCAGCCCCTCACAGTGGCCTCAAG TGTGATGCCTTACAAAAGCACCACTCAGATGGGCAGCTGGACTCTGGTGTCCTGAGACTCTGCCCTCTT CCCACAGCCTCCCTGCCCCACCCATCCCTGCAAAGCCATTTTTCAGACAGAGCCATTCCTAAGAACACT GAAGGGCTGGAATGCTGGCTGGCCACTCTCTGCCTCAGTGGCCTCCCTACAGCCTGGAAGAAGGAGGGT CCTGATTGCCAAGGAAACCTCCTCATTGGGCTAAGGAGACACTGGAGTCTGGAGTGTGGAGCCCCACAG TCTTGCAGGTCACATGCTCTCCTTGCACATCTGGCCTGGTTGTACCCACTGGCCTCTGCCTCTGCCCTG GGCCAAAAGGGCCCCTCCTTGCCAGGGGAGAGACAGCCACGGTCCTCTTTGGCCGATGCTGTATTCTCA TTTTGGCCCTTGTTCTTAGGCCCGTCTGCCCGCCTTCCTCCATCTAACCTTTCCTGTTTTATCCGCAGC CCTTTTCTTCTTTGAGTTAGTAAAGATTTATTCTGTAACCTGACACTCATCTGGCCCTTTGCAGTTTGC CAGCCATATTCCCATGTGATTTCCCACTGGATCCAGGCCCCCATCCGGCTGGCAGGAGGGGGCTCTGAC GTGCAGGTTGGAAATCAGAAGTCTGTGAGAGCGCGGGAGTGCATGGCAGCTCTGGGTCCCAGACCTGGC CCGACCCCTCTGCTTCACCTCCAGCTCTGCTGCTCCTCTACTCTTGGGTCGAGATCCCTTTGGAGCCAC AGCGAGGAACCCTGTGGTCCTCAGGCAGGTGTACCTTGAGTCAGCCAGGAGCCCTCTTTTCCTGTGTCA AAGCCTGCCCTCGGGCTCTGCTCACCTCTGGTGACCCTCCAAGATGCCCCTGCCCTCAGTTTCCCCTCA TGATCTGGCCTCTGCCCCCTTCTCTAGCCACAGCCTCTAGTACACTTTAGCAATACCACCAGACTAGTT AGAGTTCCCCACTCACCAAGCAAGACATGCAGTTTCATGCCTCTGTGCCTTCGCTCATGCTGTTTCTTC CGACTGGAATGCCTTCCCCTGCTCCTCCTGCCTTGTCTGCCTGGCAAGTTCATCTCTCACGATCCCCTC AAAGGCCCCCTCCTCCAGGAAGGCAACCCCTGTGCCCCTCCCCTCCAGGCTACCTCTGCACTTTGTCAA TGCTTCTCTTGTGGCACTTATCACACTGTATTTTACTTGTTTACATGTTTGTCTCCCCTTCTAGACTGT GAATCCTTAAGGGCATGGACTGTATCTTATGCATCTCTGTATTTCTGCGCCTAGCACGGTGCCTAGCAC ACAGTAGGCGCTCAATAAATGTTGAATGAATGAATGATTTAATCAAGA 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_015488.5 |
Synonyms | BRP17; DYT8; FKSG19; FPD1; KIPP1184; MR-1; MR-1S; MR1; PDC; PKND1; PNKD1; R1; TAHCCP2 |
Summary | This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010] |
Locus ID | 25953 |
MW | 66.3 |
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