Research Article

CYP1A1 Relieves Lipopolysaccharide-Induced Inflammatory Responses in Bovine Mammary Epithelial Cells

Figure 2

Construction of CYP1A1 overexpression plasmids and verification of overexpression efficiency. (a) Cloned full-length CYP1A1 cDNA from MAC-T cells was analyzed using PCR. (b) The dual-enzyme digestion of the plasmid of pMD19-T–CYP1A1 cDNA confirmed that CYP1A1 cDNA was accurately connected into the pMD19-T vector. (c) The efficient connection of cloned CYP1A1 cDNAs to the target plasmid was confirmed using plasmid PCR. Control: empty vector. 1, 2, and 3: target vector connected to CYP1A1 from three bacterial colonies. (d) Overexpression efficiency of CYP1A1 was verified using RT-qPCR and Western blot. GAPDH was used as an internal control. Data were expressed as the mean ± SD. versus empty vector-transfected MAC-T cells.
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