Neuroserpin (SERPINI1) (NM_005025) Human 3' UTR Clone
CAT#: SC203340
3' UTR clone of serpin peptidase inhibitor clade I (neuroserpin) member 1 (SERPINI1) transcript variant 1 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 | Neuroserpin (SERPINI1) (NM_005025) Human 3' UTR Clone |
| Vector | pMirTarget |
| Synonyms | HNS-S1; HNS-S2; neuroserpin; PI12 |
| ACCN | NM_005025 |
| Insert Size | 276 bp |
| Sequence Data |
>SC203340 3’UTR clone of NM_005025
The sequence shown below is from the reference sequence of NM_005025. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ACAAGTGGACATGATTTCGAAGAACTTTAAGTTACTTTATTTGAATAACAAGGAAAACAGTAACTAAGC ACATTATGTTTGCAACTGGTATATATTTAGGATTTGTGTTTTACAGTATATCTTAAGATAATATTTAAA ATAGTTCCAGATAAAAACAATATATGTAAATTATAAGTAACTTGTCAAGGAATGTTATCAGTATTAAGC TAATGGTCCTGTTATGTCATTGTGTTTGTGTGCTGTTGTTTAAAATAAAAGTACCTATTGAACATGTGA 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_005025.5 |
| Synonyms | HNS-S1; HNS-S2; neuroserpin; PI12 |
| Summary | This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The protein is primarily secreted by axons in the brain, and preferentially reacts with and inhibits tissue-type plasminogen activator. It is thought to play a role in the regulation of axonal growth and the development of synaptic plasticity. Mutations in this gene result in familial encephalopathy with neuroserpin inclusion bodies (FENIB), which is a dominantly inherited form of familial encephalopathy and epilepsy characterized by the accumulation of mutant neuroserpin polymers. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008] |
| Locus ID | 5274 |
| MW | 10.5 |
Documents
| Product Manuals |
| FAQs |
Resources
其它Neuroserpin产品
Customer
Reviews
Loading...
