Figure 5
From: Molecular cloning using polymerase chain reaction, an educational guide for cellular engineering

Vector and insert plasmid maps A) Illustration of the CloneJET plasmid containing the PCR product. Insertion of the PCR product in the cloning site of the plasmid disrupts the integrity of the toxic gene eco47IR and allows the growth of transgene positive clones. The plasmid was cut with the AgeI and SalI enzymes generating two fragments of 3Â kb and 0.7Â kb in size. The 0.7Â kb fragment (tdTomato gene) was used as the insert for cloning. (B) Illustration of the vector plasmid. The plasmid was cut with the AgeI and SalI enzymes generating two fragments of 4.9Â kb and 0.7Â kb in size. The 4.9Â kb fragment was used as the vector for cloning. AMP: Ampicillin resistance gene; PRE: posttranscriptional regulatory element; MPSV: myeloproliferative sarcoma virus promoter.