TCTN3 (NM_015631) Human 3' UTR Clone
CAT#: SC208752
3' UTR clone of tectonic family member 3 (TCTN3) transcript variant 1 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | TCTN3 (NM_015631) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | C10orf61; JBTS18; OFD4; TECT3 |
ACCN | NM_015631 |
Insert Size | 696 bp |
Sequence Data |
>SC208752 3’UTR clone of NM_015631
The sequence shown below is from the reference sequence of NM_015631. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTGGAGTTCTCAACCTAGAGACTATGTGAAGAAAAGAAAATAATCAGATTTCAGTTTTCCCTATGAGA AACTCTGAGGCAGCCACTTATCTTGGCTAAATAGAACCTCACCTGCTCATGACCAGAGAGCATTTAGGA TAATAGAGGACCTAACTGAAGGAATCCTTGTATATGAAAGGAGTTATTTTAGAAAAGCAATAAAAATAT TTTATTCATCATAGCTCTCTGCTTTGGGCTCTGCAGGCCACCAGATACACATGAGGCCCCTACTTCTCA AGCTGGGAAGGCCAAGAGCCTTCCTTCAGCCTTTCTGGTTATGTTACACCTAGCTGAATGTTTACAAGG TCTGGATCCATCAGCCCTCAGGCACAGTTGGGCCAAGCAGAAAGAGAGAAACACTTCTGCTGTCACCTT GAATGAACTCAGGAATAGCTTCCCTCTGGACTGTAGAGGAGCTAACTGTTTGGAACAGAAAACTGCTGG CTGTTGATTTTGTCTGGTTCCTTTGCCAACATCTGGGCACACCCTTTGCCCAGACACGAGTGGGGAAAG CAGTTCTTTCTCCTCAGTTTCCAAAGTAAATGGGGAATCCCAGCTTTCTTTTCTACTAGCAAATGACCC TACCATTTATTTCTGCCTTTTTCTTCCGTTCATTGTGAGGAAAAATAAAACTGGTTGAGAGCTTTGTTG TACTAA 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_015631.6 |
Synonyms | C10orf61; JBTS18; OFD4; TECT3 |
Summary | This gene encodes a member of the tectonic gene family which functions in Hedgehog signal transduction and development of the neural tube. Mutations in this gene have been associated with Orofaciodigital Syndrome IV and Joubert Syndrom 18. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012] |
Locus ID | 26123 |
MW | 26.7 |
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