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. 2018 Jul 31;7:135. doi: 10.1038/s41426-018-0135-9

Table 1.

Sequences of primers used in this study

Primer Sequence (5′ to 3′) Purpose Size (bp)
LB047-1 F: GCGCATATG(Nde I)AAACGATTTTGTTTG Detection and expression of LB047 gene 1317
R: GCGCTCGAG(Xho I)TTTACAACCTTGCATTTC
LB047-2 F: ATGAAACAACTTTGTTTA Detection of LB047 gene 1323
R: CTTACAAGGAGGACTTTC
LB047-3 F: TTCTGCGTGACACTCCTTAC Detection of LB047 mRNA 156
R: CTTCTTCGTCCATCAAACCT
16S-RNA F: CTTTCGTGCCTCAGCGTCAGT Inner reference in LB047 mRNA qRT-PCR 145
R: CGCAGCCTGCACTTGAAACTA
Ms-Fas F: TGTGAACATGGAACCCTTGA Detection of J774A.1 Fas mRNA 177
R: TTCAGGGTCATCCTGTCTCC
Ms-FasL F: CATCACAACCACTCCCACTG Detection of J774A.1 FasL mRNA 162
R: GTTCTGCCAGTTCCTTCTGC
Ms-actin F: AGAGCGGGCCTTGAGAAAAG Inner reference in J774A.1 Fas/FasL mRNA qRT-PCR 111
R: TGGAGAGCCTGGATTGTCATC
Hu-Fas F: AGCTTGGTCTAGAGTGAAAA Detection of THP-1 Fas mRNA 180
R: GAGGCAGAATCATGAGATAT
Hu-FasL F: CACTTTGGGATTCTTTCCAT Detection of THP-1 FasL mRNA 160
R: GTGAGTTGAGGAGCTACAGA
Hu-actin F: ATAGCACAGCCTGGATAGCAACGTAC Inner reference in THP-1 Fas/FasL mRNA qRT-PCR 158
R: CACCTTCTACAATGAGCTGCGTGTG

Underlined areas indicate the sites of endonucleases

F forward primer, R reverse primer, Ms mouse, Hu human