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. 2020 Sep 28;101(6):203–214. doi: 10.1111/iep.12366

Figure 2.

Figure 2

CCL‐18 was a direct target of miR‐484. A, The prediction of the binding between miR‐484 and CCL‐18 by TargetScan. B, Luciferase reporter assays were performed to verify the binding of miR‐484 in 3′‐UTR of CCL‐18. * P < .05 compared with that of miR‐NC. C, Western blot was used to demonstrate weather miR‐484 target to regulate CCL‐18. * P < .05 compared with that of control; #P < .05 compared with that of miR‐484 + vector