Expression of SPM Receptor Genes in Gingival Tissue Samples via qRT-PCR

CL Chun-Teh Lee
RL Ruoxing Li
LZ Lisha Zhu
GT Gena D. Tribble
WZ W. Jim Zheng
BF Brittney Ferguson
KM Krishna Rao Maddipati
NA Nikola Angelov
TD Thomas E. Van Dyke
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Expression of SPM corresponding receptor genes was analyzed with qRT-PCR, utilizing the TaqMan Gene Expression Assays Protocol (Applied Biosystems, Foster City, CA, USA). Details of the experiment were previously described (21). The TaqMan Assay primers included GAPDH (assay ID: Hs99999905_m1, Applied Biosystems) as the housekeeping gene compared to ALX (FPR2) (assay ID: Hs00265954_m1, Applied Biosystems), BLT1 (LTB4R) (assay ID: Hs00175124_m1, Applied Biosystems), ChemR23 (ERV1) (assay ID: Hs01386063_m1, Applied Biosystems), GPR18 (DRV2) (assay ID: Hs00245542_m1, Applied Biosystems), GPR32 (DRV1) (assay ID: Hs00265986_s1, Applied Biosystems), GPR37 (assay ID: Hs0017374_m1, Applied Biosystems),and LGR6 (assay ID: Hs00663887_m1, Applied Biosystems), which were labeled with FAM dye. The calculated cycle threshold (Ct) values from each sample were obtained and relative expression (2-ΔΔCt) was calculated to determine expression of specific SPM receptor genes between groups.

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