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. 2018 Mar 23;8:91. doi: 10.3389/fcimb.2018.00091

Table 1.

Primer sequences used for RT-PCR.

Genes Forward Reverse
Enterokinase
   For all variants GCACCTGATGGCCACTTAAT CCAGTCACTGCTGACGAGAG
   To discriminate among variantsa GAGTCATGAAGCCAGAGCGACATTTA TGTCTTCGTCAGAACCATCTGGACA
TMPRSS2b TAACTGGTGTGATGGCGTGT CCGCTGTCATCCACTATTCC
TMPRSS4 CTGAACAGCCTCGATGTCAA CAAGGGACAGTCCAGCTCTC
HATc TCACCAGCTACACASGAATACAG GAAATTTCATGACAACATCCGC
PRSS1d CCACCCCCAATACGACAGGAA TAGTCGGCGCCAGAGCTCGC
PRSS2d CCACCCCAAATACAACAGCCG GGGTAGTCGGCACCAGAACTCAG
PRSS3e CGCCACCCTAAATACAACAGGGA TGGGTAGTCAGCACCAAAGCTCAG
β-Actinf ACTGGGACGACATGGAGAAA GGGGTGTTGAAGGTCTCAAA

The cDNAs were amplified in 45 cycles (10 s denaturation at 98°C, 10 s annealing at 60°C, and 30 s extension at 70°C) except for

a

annealing temperature: 66°C.

b

annealing temperature: 63°C.

c

annealing temperature: 55°C.

d

annealing temperature: 62°C.

e

annealing temperature: 58°C.

f

amplified in 40 cycles.