KALRN (NM_007064) Human 3' UTR Clone
CAT#: SC216272
3' UTR clone of kalirin RhoGEF kinase (KALRN) transcript variant 3 for miRNA target validation
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CNY 5795.00
货期*
                        3周
                    规格
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                Specifications
| Product Data | |
| Product Name | KALRN (NM_007064) Human 3' UTR Clone | 
| Vector | pMirTarget | 
| Synonyms | ARHGEF24; CHD5; CHDS5; DUET; DUO; HAPIP; TRAD | 
| ACCN | NM_007064 | 
| Insert Size | 2000 bp | 
| Sequence Data | >SC216272 3’UTR clone of NM_007064  The sequence shown below is from the reference sequence of NM_007064. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATTGTCAACCGGGTGAACCAAGGGACGTAGCCATCTCCCAGCCCCTATGGTTTCACATAGACGTGCAGT GTGAACCAAAGCAAGACTGAATGTGACTGTAAATAATTCTGTTCATCATTTCACTCCGTGCAGTTCTCT GAATTGAGAGATGTACCTCTTAAACCTCGTCAGTGGTTATTCAGGGTCTGAGCAGCAGTAAAAGTCACC CTAAATCAAGGGGCTTTTCAGAAGGTCATTCTGAAGAAATAAAGAGGCAAAGGGTCACAGAAGTGTTCA GAAGAAGGGCAAAGATAAGAACAATATTAGCTGTTACGAAATTTTAACTGTATCTTCCAAAATGAGTGG TTAACTGGGCAAACCTTAAGCTCACAAGAGTATAAAAGATCTCTGGCTTTGCTGAAATTTTAAGCAAGA AGTTCTATTTAATGGAGATGTCATGTATATCAACTATTCTGGTTTAGATAACTTAGATATAGTTTCTTA ATAGGATAGATACCCACATACAGTATAATATATCCCATTCAGGTTTCAGAGTTTTCTAATATAGAGATA TATATATTAAATCAATCACAAGTAATTTTGAGTGCTCCAGTTAAGACAGTAATTTATTTACCGAATCAT TACATTGTTTTGACTAAGCACAATTAGATGACAAGTTTTTTTAGAGCATTTTATAGATCTTGTATAGAA ATCTTTTACCAGAACCTGTGCATTAAGAGAAAGCAATGTTGCCCTTTTGAATGAGAAAATTTTTTCTGT CAATCGCAGGTTATTTGATTAAGATAGGTTCTTTCTGTATATGAAACGCTCCCCGCAAATTCACTGGCA GCTCAGAATTATTCTGGAAAGAAAGCCTGCCAGGAAATAAATTCAAATACAGTATGAGCTGCGGGGATA TTTTTGTGTCTACACCAGGTTTGAAATAAGTAAACAAATACAAGAGGTTCATATAAAAGGGCAAATGAA AACCTTTCCTACAGTTCCTATGAACAACGTACCAACACTTTCTGATTTCTTCTACAGCTGTAGAATACC ATCTTTCAGAAAGTTGGCTGGCTTTATTTCTAACTCCTTATTGAAGCTAAGGGGTGCTTACTAAAAGGA GGCAGCCATATAGGCCTTTTAAAGGCCTGGTTCTAAGTCCTTTTTAAAGCCATGGAACAAAACCTGATA CATCACCCTAACAGAGCATTAAGTTGTAACTGAGATTGCAATACCTGTCACCATGCAGCCGCTGATAGT TCTCTGAACTAAAAGGACTAATTGTACTTTGAGGCCAATGCTGCTTTCTGGTGTATATTCTCCATACAA GATTATTATTAACTGCTCTTTTTCCCTCTGGTGGAAAAAAAATTAAACCTGGGCATTTCATGGGTTTTC TTTCTTTATTTTTGTTCATTTGTTTTGGAGGGAGGGAGCTTGTTTTTTGTGTTTGTACATGATCCACCC TTAGTTTTCTAGAATGTGTGTTGAAAATTGCGATTATACAAGTAAGATTTTAAAAATGTAACTCAAGTG TTTGTTCAAATCAGGTTTAATGGTGTTGCTTCTCTCCTATAATGGGATAGAGAAAATTAAAATCACGTA GTACAGAAGTGCAAGAAGAGAATTTATGAAGGATGAATAGAACTACAAACCTATCTAAATGAAAAAGAA ATGGTGGAAACTAAGCCTGAACTTTAACATATAAAAAACACTTATTCCCACAGAGAAAATGTAAAATTA AAAATCATCATCTTTTTTTTTCCATTGGTTTCAAAGACAACTTCCTCATTCGCCCTCCACCTCATCCCA TCCAAGATTATAGATTGATAAATTAATGGAAAGTATAAGCAATAAGACTAGATAGCACTTAGTATTTTT GGGATTAACCAAATATATGGAAACCGACTCCGACTGTATTTGTTTCTTAATTTTCAAATGGCCCTGGGT CATAAAGCCTCACTCCCTCAGAGGTCTCTCGACTAACCCCTATAGTCTTCATTTGGACCTTTATGTAT 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_007064.5 | 
| Synonyms | ARHGEF24; CHD5; CHDS5; DUET; DUO; HAPIP; TRAD | 
| Summary | Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016] | 
| Locus ID | 8997 | 
| MW | 77.4 | 
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