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. 2020 Jan 27;11(1):68. doi: 10.1038/s41419-020-2263-0

Table 1.

Universal ProbeLibrary RT-qPCR assays used in this study.

Gene name Accession number Forward primer sequence Reverse primer sequence Probe
BCL-GS NM_030766 CAGGAGATCAGTTGGAAAGAAAG CTGGTGTCAACCAAGGGAAT 8
BCL-GL NM_138722 CCCCAGAGAATTCCTTGAGTC TCATCATCATCTAGGGGGATTT 85
BCL-GL NM_138722 GCTTTAAGGCTGCCCTTGTA TCATCGGGTGGTTGTCAAT 100
STAT1 NM_007315 GGATCAGCTGCAGAACTGGT CTGTTCCAATTCCTCCAACTTT 74
p65/RelA NM_021975 ACCGCTGCATCCACAGTT GATGCGCTGACTGATAGCC 47
BRM NM_003070 GATTCAGCCAGCACACTCCT GGCGTGGACATCTACCTCTC 53
BRG1 NM_001128849 TGGACCAGCACTCCCAAG CTGGCTGGAACTGGACTAGAG 21
LGR5 NM_003667 ACCAGACTATGCCTTTGGAAAC TTCCCAGGGAGTGGATTCTAT 78
MUC2 NM_002457 GCCAGCTCATCAAGGACAG GCAGGCATCGTAGTAGTGCTG 61
VIL1 NM_007127 GCAGCATTACCTGCTCTACGTT GCTTGATAAGCTGATGCTGTAATTT 71
ACTB NM_001101 ATTGGCAATGAGCGGTTC CGTGGATGCCACAGGACT 11

For BCL-G overexpression studies, relative mRNA levels of BCL-GL were measured using Universal ProbeLibrary RT-qPCR assay, probe 100.