EXOSC3 (NM_001002269) Human 3' UTR Clone

CAT#: SC207360

3`UTR clone of exosome component 3 (EXOSC3) transcript variant 2 for miRNA target validation


Reconstitution Protocol

USD 560.00

4 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol EXOSC3
Synonyms bA3J10.7; CGI-102; hRrp-40; p10; PCH1B; RRP40; Rrp40p
ACCN NM_001002269
Insert Size 554
Sequence Data
>SC207360 3'UTR clone of NM_001002269
The sequence shown below is from the reference sequence of NM_001002269. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon


CAATTGGCAGAGCTCAGAATTCAAGCGATCGC

GCAGGCTATTAGCTCCAGATTGTGAAATCATACAGGAAGTGGGAAAACTCTATCCACTGGAGATAGTATT
TGGAATGAATGGAAGAATATGGGTTAAGGCAAAAACCATCCAGCAGACTTTAATTTTGGCAAACATTTTA
GAAGCTTGTGAACACATGACGTCAGATCAAAGAAAACAGATCTTCTCCAGATTGGCAGAAAGTTGATATA
GGTGGACTTTTTTACAGGTCAGTTGAGGCAAAAAACTATGGGTTTTTTCAGGTGAACCTCCCCCATTTAA
ATACTCAGAAGATAAGGTGTGAATGTATGTATTATTAGAGTCCGAAAGTATTTTTATAAGTTACTGGTTT
TCACCCACGCTTTTGTGGGAGAGAAAATCATTGCAAAATCATTTTTTTTGTTCGGTACAATAAAGTTTAC
TAAAAAACAGTATTAGGGTTTATTTGGAGTTAACTCCCTTAGTAATTGCTACAGCTTCCATAATTAACTG
GAGGTCAGCAGTAAAATAATTTTGTGATTATAACAGTAAGCCAGGTTCACCAGAGGAAATGTGG

ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_001002269.1
Summary This gene encodes a non-catalytic component of the human exosome, a complex with 3'-5' exoribonuclease activity that plays a role in numerous RNA processing and degradation activities. Related pseudogenes of this gene are found on chromosome 19 and 21. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jun 2012]
Locus ID 51010

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