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. 2018 Feb 23;8(16):8455–8468. doi: 10.1039/c8ra00296g

Primers used in this study.

Primer sequences Restriction enzyme cutting site
pcDNA-linc00472 BamHI and XhoI
Forward CGGGATCCATGCGAGGCTGGGGCCGGTTG
Reverse CCGCTCGAGTTTAGACTCCAAATGGCTG
pmirGLO-linc00472-WT SacI and XhoI
Forward CGAGCTCACCCTCTACCTTTCCAATC
Reverse CCGCTCGAGGTTACCTATCACTTCCTTTCG
pmirGLO-PDCD4-WT SacI and XhoI
Forward CGAGCTCATATAAGAACTCTTGCAGTC
Reverse CCGCTCGAGACCAGGTTCATTTTTCC
pLenti-puro-linc00472 BamHI and EcoRV
Forward CGCGGATCCATGCGAGGCTGGGGCCGGTTG
Reverse GCGCGATATCTTTAGACTCCAAATGGCTG
pLenti-puro-pre-miR-141 BamHI and EcoRV
Forward CGGGATCCGGGTCCATCTTCCAGTAC
Reverse GCGCGATATCGAGCCATCTTTACCAGAC
miR-141 (reverse transcription primer), linc00472 (quantification primers) GTCGTATCCAGTGCAGGGTCCGAGTATTCGCACTGGATACGACGCTGA
Forward CACTGGGCATTTTCTCTTCA
Reverse CCTATCCCTTTCCCTCTGCT
PDCD4 (quantification primers)
Forward GGCCTCCAAGGAGTAAGACC
Reverse AGGGGTCTACATGGCAACTG
β-Actin (quantification primers)
Forward GCATCCCCCAAAGTTCACAA
Reverse AGGACTGGGCCATTCTCCTT
miR-141 (quantification primers)
Forward GCCGCTGTAAACATCCTACACT
Reverse GTGCAGGGTCCGAGGT
U6 snRNA (quantification primers)
Forward CTCGCTTCGGCAGCACA
Reverse AACGCTTCACGAATTTGCGT