FLCN (NM_144606) Human 3' UTR Clone
CAT#: SC202688
3' UTR clone of folliculin (FLCN) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
Product images
经常一起买 (2)
Specifications
Product Data | |
Product Name | FLCN (NM_144606) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | BHD; DENND8B; FLCL |
ACCN | NM_144606 |
Insert Size | 1842 bp |
Sequence Data |
>SC202688 3’UTR clone of NM_144606
The sequence shown below is from the reference sequence of NM_144606. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGGGAAGCTCACCCTCCGATCTCGGTGTGATTGTTGTGATTGTTGTGATTTCCTGTCTCGTTTGCCTTG ACCGCCATGTGAAAGAATCTGTTCCCCAGCTAGGTGGGGAAAATTCACAGGTGGGCTGTCTGTAGAGAG AACTGGCTGATTAAAGGCTTCTCGTCCCGATTTTGTGATAGCCAAGTGCTTGGCCTGGTCGACGGTCTT TGCTCCTTTACAAATAAAGTGTTCTGTTTCAGTTCGTCCCAAGTTTTCCATGAAGGGCAGTGGTTCCCT GACCTCCCAGGTGCCTGGGCTTCCCCAGGTTCCTGATCTGGGGCTTGGGGCCCTGTGTTTGGGGATCGT GGCACTGTGTGCACCAGCCTGGAAGCACTGGGCCAGTCTTGGCCAAGCTTTCCATCAGGGATGATTTGA TCTTGGTGCTACAGGTCTGTGGTACGACCATTGTTCCACACCACATGTCATTAATAATGCTTCCCATGC TTCTGCTTGCAAATGACCAGCCTTCCAAACAGCCAGAGCTGTTTCGAGGTGTTTCTGCAGGCAGGTGCA GGCGTGCCCTCAAATAAGCTTTGCCAATGGAGTCTCAGCAAGAGCAAAACCTGGTCAGGAAAGACAAAG CCTGGGAATCCACCCCCATGCCCTGCAGGTTGGCTGGCCCTGGAGCCATTTATTATAGTGCTAATCATG TTTCTAGGCAGGTGCAGATGGCAAGGGCAGTGTCTTGGTGAGCTTTTTAGCACGAAGAGCCAGGTCTGT CGAAGCCTTTGTGAGAGCTGGAAACGCAGGTGTGCTGGGCATGCGCAGTATGGGGTTTCGGGCTCAGGG CTTGCCCTTTGGCATCAGACAGACCTGGCTTCGCATCCTGGATTTGCTTCTGACGTGCACCCTTCCCTT TGGGTCTCGTGATGTGAAATGGAGATGTTGTCATTTGTGAGGGCTCCATGAAGTTTCGTTGAAATGACA AATACTAATTTCTTCATCTGTGAAATGGAGATAATAGTGCTGACCTCAGAACAGCTGAGAGGACTAAAT GAAATGATGTTGGATGTAGCCATAAAGAACGAAGTCAGGCACTGGTGCACGCCTGGAATCCCAGCTCTT GGGAGACCGAGACAGGTGGATTGCTTGAGCTCAGGAGTTTGAGACCAGCCTGAGCAACATAGGGAGGTC CAGTCTCTACAAAAAATATGAAAAGTAGCTGGGCGTGGTGGCGCATGCCTGTAGTCCCACTACTTGGAA GGCTTCGTTGGGAGGATCACTTGAGCCCAGAAGATTGAGGCTGCAGTAAGCCGTGATCGTGCCACTGCA TTCCAGCCTGGGCAACAGAGCGAGACACTGTCTCAAATAAAAAAGATGGGAATAGTAGACACTGGGGGC TCCAGAAGGAGGGAGGGAGGGAGGAAGGGGAGGAAGGGCTGAAATGCTTTCTATTGGATACTATCTGGG CATATTACTTCCTGTGGTTCACTGTCTGGGTGACAGGATTCATAGAAGCCCAAACTTTAGCACCACGCA GCATACCCTTGTAACAAAGCCGCACACGTACGCCCTCAAGCTAAAACAAAAGTGGACCGGGAGGCCGAG GTCGGGGGATCATGAGGTCAGGAGTTTGAGACCAGCCTGGCAGATAACGGTGAAACCCCGTCTCTACTA AAAATACCAAAAAAAGTTAGCCGGACATGGTGGCAGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGGG GCAGAAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGC CTGTGCGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAA 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_144606.7 |
Synonyms | BHD; DENND8B; FLCL |
Summary | This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008] |
Locus ID | 201163 |
MW | 68.1 |
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