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
    • 10 ug

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DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1280.00

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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