TCTN1 (NM_001082537) Human 3' UTR Clone
CAT#: SC200685
3' UTR clone of tectonic family member 1 (TCTN1) transcript variant 2 for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CNY 4845.00
货期*
3周
规格
Product images
推荐一起购买 (2)
Specifications
| Product Data | |
| Product Name | TCTN1 (NM_001082537) Human 3' UTR Clone |
| Vector | pMirTarget |
| Synonyms | JBTS13; TECT1 |
| ACCN | NM_001082537 |
| Insert Size | 419 bp |
| Sequence Data |
>SC200685 3’UTR clone of NM_001082537
The sequence shown below is from the reference sequence of NM_001082537. 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_001082537.3 |
| 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 |
Documents
| Product Manuals |
| FAQs |
Resources
Customer
Reviews
Loading...
