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. 2016 Sep;28(9):1380–1388. doi: 10.1016/j.cellsig.2016.06.015

TABLE 1.

Sequences of various primers used in this study. F – forward and R – reverse, RT – reverse transcription.

Designation Sequence Used in
sh-1 CCGGCGGGTACACAAATGGAGTGAACTCGAGTTCACTCCATTTGTGTACCCGTTTTTG Knockdown of RPIA
sh-2 CCGGGCTGATGAAGTAGATGCTGATCTCGAGATCAGCATCTACTTCATCAGCTTTTTG Knockdown of RPIA
sh-3 CCGGGAATTGGAAGTGGTTCTACAACTCGAGTTGTAGAACCACTTCCAATTCTTTTTG Knockdown of RPIA
sh-4 CCGGGAAGTGAATACAGCTATCAAACTCGAGTTTGATAGCTGTATTCACTTCTTTTTG Knockdown of RPIA, pMOWS cloning
RT-RPIA F GGCGGTGCTGGCAACACAAG RT-PCR
RT-RPIA R TGGCGGGCCTGGAAGGAAGT RT-PCR
GAPDH F GAAATCCCATCACCATCTTCCAGG RT-PCR
GAPDH R GAGCCCCAGCCTTCTCCATG RT-PCR
sgRNA-R CACCGGCCGCACGTGGGAACCCGGG CRISPR reverse strand nicking
sgRNA-F CACCGTGCCGGGGCGTGCACAGTCT CRISPR forward strand nicking
CRISPR gen F GCGAATCCAGATAGGGGTTCCTCGAAGC CRISPR - genomic PCR
CRISPR gen R GCAAGCTTAGCAGGGAAGAGGGGTCTAA CRISPR - genomic PCR