CXCL16 participates in pathogenesis of immunological liver injury by regulating T lymphocyte infiltration in liver tissue

Figure 3 Detection of CXCL16 mRNA in the injured liver by real-time quantitative RT-PCR analysis. Total RNA was isolated from the liver tissues at the different group as indicated and then reverse transcribed with reverse transcriptase and amplified by real-time quantitative PCR specific for CXCL16. Amplification of b-actin by same approach was used as control. The results represent three independent experiments. ^aP<0.05 vs normal mice, ^cP<0.05 vs BCG-primed mice.