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. 2021 Feb 23;2:100023. doi: 10.1016/j.crmicr.2021.100023

Table 1.

Primers used for PCR amplifications.

Gene Protein Primer sequence (5′ – 3′)
P2RX7 P2 × 7 Forward: TTCAGGCAGGCAGTATCACTC
Reverse: CCACGGGAAAGACACAGGTAG
CASP11 Casp-11 Forward: ATGGCTGAAAACAAACACCCT
Reverse: TCAGTTGCCAGGAAAGAGGTAG
CASP1 Casp-1 Forward: GGAAGCAATTTATCAACTCAGTG
Reverse: GCCTTGTCCATAGCAGTAATG
IL1B Il-1β Forward: TTCAGGCAGGCAGTATCACTC
Reverse: CCACGGGAAAGACACAGGTAG
TNF Tnf-α Forward: TTCAGGCAGGCAGTATCACTC
Reverse: CCACGGGAAAGACACAGGTAG
NLRP3 Nlrp-3 Forward: GCT CAG CTC TGA CCT CT
Reverse: AGG TGA GGC TGC AGT TGT CT
TNFRSF11A Rank Forward: TTAAGCCAGTGCTTCACGGG
Reverse: ACGTAGACCACGATGATGTCGC
TNFSF11 Rankl Forward: CAGAAGATGGCACTCACTGCA
Reverse: CACCATCGCTTTCTCTGCTCT
Fusobacterium nucleatum (Target Species) Foward: CTT AGG AAT GAG ACA GAG ATG
Reverse: TGA TGG TAA CAT ACG AAA GG
Porphyromonas gingivalis (Target Species) Foward: CGCAGACGACAGAGAAGACA
Reverse: ACGGACAACCTGTTTTTGATAATCCT
ACT β-actin Forward: TAT GCC AAC ACA GTG CTG TCT GG
Reverse: TAC TCC TGC TTG CTG ATC CAC AT