Reticulon 2 (RTN2) (NM_005619) Human 3' UTR Clone
CAT#: SC206091
3' UTR clone of reticulon 2 (RTN2) transcript variant 1 for miRNA target validation
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CNY 4845.00
货期*
3周
规格
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Specifications
Product Data | |
Product Name | Reticulon 2 (RTN2) (NM_005619) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | NSP2; NSPL1; NSPLI; SPG12 |
ACCN | NM_005619 |
Insert Size | 444 bp |
Sequence Data |
>SC206091 3’UTR clone of NM_005619
The sequence shown below is from the reference sequence of NM_005619. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTCTCCGGATCCAAAGCCAAAGCCGAATGAGAACGGTGTCTCTGCCCGCAGGACGCCTGCCCCCAGCCC CCGCAGCCCTCTGGCCCCCTCCATCTCTTGTCCGTTCCCACCCACCCCCCTCCTCGGCCCGAGCCTTTT CCCGGTGGGTGTCAGGATCACTCCCACTAGGGACTCTGCGCTAATTACCTGAGCGACCAGGACTACATT TCCCAAGAGGCTCTGCTCCAGGAGTCCAGGAAAGACGAGGCACCTTGGCCGCGGGGCCTGCTGGGACTT GTAGTTGCCTAGACAGGGCACCACCCTGCACTTCCGGACCCGCCGCTGGAGGCGCCGTGAGGCGTTGGT GTCTCCTGGATGCTACTAGCCCCAACGCCGGGGCTTTGCATGGGGCCCAGGGGAGGCCTGAGCTTGGAT TTACACTGTAATAAAGACTCCTGTGGAAAA 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_005619.5 |
Synonyms | NSP2; NSPL1; NSPLI; SPG12 |
Summary | This gene belongs to the family of reticulon encoding genes. Reticulons are associated with the endoplasmic reticulum, and are involved in neuroendocrine secretion or in membrane trafficking in neuroendocrine cells. Reticulon proteins also play an important role in the replication of positive-strand RNA (ssRNA) viruses. Mutations at this locus have been associated with autosomal dominant spastic paraplegia-12. [provided by RefSeq, Aug 2020] |
Locus ID | 6253 |
MW | 15.7 |
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