Meckelin (TMEM67) (NM_001142301) Human 3' UTR Clone
CAT#: SC215988
3' UTR clone of transmembrane protein 67 (TMEM67) transcript variant 2 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 | Meckelin (TMEM67) (NM_001142301) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | JBTS6; MECKELIN; MKS3; NPHP11; TNEM67 |
ACCN | NM_001142301 |
Insert Size | 1715 bp |
Sequence Data |
>SC215988 3’UTR clone of NM_001142301
The sequence shown below is from the reference sequence of NM_001142301. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACATTGGTGGATCAAAGATTTTTGATTTAACTTCCTGAATAAATAACTTAAAGACTCAGTATAATCATG GCCAAAAAAAAGTCATGATATCAGGTTAGTTTGCCATATTTTTTAAAACTTATAATGCAGACTATTCTG TTTTTGTTTTTTATTTGCAGAAAGATTTATTTTTATAACTTGGGAATATATAACCTGATATAATAGAAA ATACTGTTTTCCCATTGTGTGTAGTATTTAATGCAGTAAATAATAAATTAATACTGACAGTGAGGCCAA AAAAAATCTAAATGTTGCTTTCAGCATAATACTTTTTAATGCTAATTAAAACAGTCCCCATCATTTGTC TCTGTAGATTATTTTATAAACTGAGAGCTGCCTGAATCTTCTCACATTGACAAAGTAATTTGATTCCAA GTTTAAGACTAGTTTTCAGTTTGATATTTTCATGTTTTGTGTGCTTATGGTTAAATAAATGTTGAAAGA TATTTTCAAGTTTACTTAGAAATTTTAAATTGTATTATTGCTGATTCAATTTGCATCATTCTAATTGCT CATCCTCTTTGGCAGTGGATTAATTCACTGTTGGGTTAATATGCATCTCATGAAATGATATCTTTTCAT TCCTTTGTATACCTGTATTAGGTCAGTATACGCTTTCCATGAAATATATTTGCATTTCTAATATAGTTT ACATTTATTAAGTTATAACGTATGACATTTTTCCCAATATCATTTTTTATACATTTTAATTACTTAATG TTTTAAGAGTTCTCTTCCAGAGTTTTGCTTTTCAATTACGTTTAAAGACTGTAAATAACAAACAGTAAG GCTGGGCGCTGTGGCTTACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGCACGTGGATCACTTTAGG TCAGGAGTTCAAGAACAGCCTGGCCAACATGGAAAACCCCATCTCTACAAAAAATACAAAAATTAGTTG GATGTGGTGGCCTGTAATCCCAGCTATTTGGGAGGCTGAGGCATGAGAATAGCTTGAAACCAGGAGGTG GAGGCTGTAGTGAGCCAGATAGCACCACTGCACTCCAGCCAGGATGACAGAGCAAGACCCTGTCTCAGA AAAAACAAAAACAAAACACTGTAAATGTATCATGTTTCTCACTGCTTTCTATGTTAATGCTGTGTAAAT ACTTAAAATGGAATACTGTATAAATATTATTTATATTTTCTCAGATGAAAATATATACTAAAACATTTG GTATTTCTGTTTTCTGTTTCATTAATGTATATCTGATGGAGTACCATTTAGGAATATAACATTATTGGG GCAGAGGTCCCAGCCATTGCCAAAGTTGAATCTTTTACATTTCCCTGAATCTTGAGGATGACTGAAAAG GAAGTCTTTGAAACTGCAGTTTCTGAAGGATCACAGTACAGGAATGCCTTTATAAAAGCTGCAGAGATA AATACATGTACTTATATGGCATGGATATTTAAAACCACTCACTCAGAAGCATATGAAAGAAATTCAACC ATCATTCAACATAGAAGAAGTTAATTTTAGTGCAAAAGTTTTTAAGTATTAAATTTCACAATAAAGGAT CAATTGGCTTACTTGCTGATAAATTAAAACAGAAAACATTTAAAATCATTCTAAATTTTGTATGATATT TTTATTTTGGCTAGGTGCATAAAAATGTGTTCAGATTTTCAAAAAAAAAAAAAAAAAAA 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_001142301.1 |
Synonyms | JBTS6; MECKELIN; MKS3; NPHP11; TNEM67 |
Summary | The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008] |
Locus ID | 91147 |
MW | 67.4 |
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