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 5,795.00
货期*
3周
规格
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经常一起买 (2)
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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