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. 2020 Jun 2;21(11):3989. doi: 10.3390/ijms21113989

Table 4.

qPCR Primers.

miRNA Primer Sequence 5′ to 3′ a R2 Amplification Efficiency (%)
miR-155-5p b TTAATGCTAATCGTGATAGGGGT 0.999 81.3
miR-146b-5p TGAGAACTGAAGTCCATAGATGG 0.986 104.6
miR-146a-5p b TGAGAACTGAATTCCATAGATGG 0.989 115.9
miR-126-3p TCGTACCGTGAGTAATAATGCA 0.984 107.2
miR-150-5p TCTCCCAATCCTTGTACCAGTG 0.992 113.9
miR-2188-3p GCTGTGTGAGGTCAGACCTATC 0.982 116.5
miR-139-5p TCTACAGTGCATGTGTCTCCAGT 0.974 100.9
miR-221-5p ACCTAGCATACAATGTAGATTTC 0.984 115.4
miR-200ae-3p TAATACTGCCTGGTAATGATGAT 0.952 82.3
Normalizers
miR-125a-5p TCCCTGAGACCCTAACTTGTGA 0.994 115.1
miR-19c-3p TGTGCAAATCCATGCAAAACTG 0.990 104.1

a Mature miRNA sequences were used as the forward specific primer, whereas a universal primer was used as a reverse primer. All primers showed no amplification in the no-template controls and generated an amplicon with a single melting peak. b 4-point serial dilution curve was used.