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. 2019 May 15;11(5):272. doi: 10.3390/toxins11050272

Table 3.

Primers used in this study.

Primer Sequence (5′-3′) Use
FGSG_TRI5-qF CACTTGTCAAGGAGCACTTTC qRT-PCR for determining the expression of TRI5 (FGSG_03537)
FGSG_TRI5-qR TGCTCAATCCAACATCCCTC
Actin-qF ATCCACGTCACCACTTTCAA qRT-PCR for inter-reference actin
Actin-qR TGCTTGGAGATCCACATTTG
FGSG_00500-qF CGACCTCCACGACAACA qRT-PCR for determining the expression of hexokinase (FGSG_00500)
FGSG_00500-qR GATAGCAGCAACGCCACA
FGSG_09456-qF GATAGATTGGAGAGCCGAGAGA qRT-PCR for determining the expression of 6-phosphate fructokinase (FGSG_09456)
FGSG_09456-qR GAGGTGCTGGATACACTTGATG
FGSG_07528-qF GAGATCCGAACTGGTAAGACTC qRT-PCR for determining the expression of pyruvate kinase (FGSG_07528)
FGSG_07528-qR CGTCAGAAGCGGTAGCATAA
TRI1-GFP-F ACTCACTATAGGGCGAATTGGGTACTCAAATTGGTTTTGTGAGTAGGCCTCATA A pair of PCR primers to amplify TRI1(FGSG_00071) fragments used for construction of the TRI1-GFP, vector under its own promoter
TRI1-GFP-R CACCACCCCGGTGAACAGCTCCTCGCCCTTGCTCACGTCATCCTGTACCAATTCCAATCG