CLDN5 (NM_001130861) Human 3' UTR Clone
CAT#: SC207859
3' UTR clone of claudin 5 (CLDN5) transcript variant 1 for miRNA target validation
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CNY 5,464.00
货期*
现货
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CLDN5 (NM_001130861) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | AWAL; BEC1; CPETRL1; TMDVCF; TMVCF |
ACCN | NM_001130861 |
Insert Size | 581 bp |
Sequence Data |
>SC207859 3' UTR clone of NM_001130861
The sequence shown below is from the reference sequence of NM_001130861. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC CGGCGACTACGACAAGAAGAACTACGTCTGAGGGCGCTGGGCACGGCCGGGCCCCTCCTGCCAGCCACGC CTGCGAGGCGTTGGATAAGCCTGGGGAGCCCCGCATGGACCGCGGCTTCCGCCGGGTAGCGCGGCGCGCA GGCTCCTCGGAACGTCCGGCTCTGCGCCCCGACGCGGCTCCTGGATCCGCTCCTGCCTGCGCCCGCAGCT GACCTTCTCCTGCCACTAGCCCGGCCCTGCCCTTAACAGACGGAATGAAGTTTCCTTTTCTGTGCGCGGC GCTGTTTCCATAGGCAGAGCGGGTGTCAGACTGAGGATTTCGCTTCCCCTCCAAGACGCTGGGGGTCTTG GCTGCTGCCTTACTTCCCAGAGGCTCCTGCTGACTTCGGAGGGGCGGATGCAGAGCCCAGGGCCCCCACC GGAAGATGTGTACAGCTGGTCTTTACTCCATCGGCAGGGCCCGAGCCCAGGGACCAGTGACTTGGCCTGG ACCTCCCGGTCTCACTCCAGCATCTCCCCAGGCAAGGCTTGTGGGCACCGGAGCTTGAGAGAGGGCGGGA GTGGGAAGGCTAAGAATCTGC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_001130861.1 |
Synonyms | AWAL; BEC1; CPETRL1; TMDVCF; TMVCF |
Summary | This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets. Mutations in this gene have been found in patients with velocardiofacial syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, May 2018] |
Locus ID | 7122 |
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