TCTN1 (NM_001082538) Human 3' UTR Clone
CAT#: SC200689
3' UTR clone of tectonic family member 1 (TCTN1) 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 | TCTN1 (NM_001082538) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | JBTS13; TECT1 |
ACCN | NM_001082538 |
Insert Size | 419 bp |
Sequence Data |
>SC200689 3’UTR clone of NM_001082538
The sequence shown below is from the reference sequence of NM_001082538. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCCTTTAACTTCTTCTTCCCGTTTGTTTGACAATGCTCAGATGCATCAGTTCCTTAATATACACGTGAA ATTTGAAAACTGTACATTCGGTGAGATTAAATTTTATATACAACTAGCAATTGTCCAGCTTTGTTGCTC ATTTTCAATTAAGGCTAAAGTGTTCAACATGAGAAAATGTGATACATTTGATACAGTGTGGGGTGGGAG TGGATGGGCAGCTCTTGGTGGTACTGGACCTTCCACAAGGCTGTGTCCACCCAGAATCCATGCTGGCAG GAGGGAGGCAGAGGTATCAAACCAAACCTCTCACCAAGCGGCCCAGGAGGGGCAGCTGTTCCTCTCGTG ACAGCACAGGCCCATGAGACAGTGTCTTCTTTTTGAGGGGAGCTGGTCCGGGTCTAGTTCACTTCACCA AGAAG 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_001082538.3 |
Synonyms | JBTS13; TECT1 |
Summary | This gene encodes a member of a family of secreted and transmembrane proteins. The orthologous gene in mouse functions downstream of smoothened and rab23 to modulate hedgehog signal transduction. This protein is a component of the tectonic-like complex, which forms a barrier between the ciliary axoneme and the basal body. A mutation in this gene was found in a family with Joubert syndrome-13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
Locus ID | 79600 |
MW | 15.8 |
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