I have a list of questions I have while studying for my course called Introduction to genetic engineering ad I have a couple of questions i hope I can get answered. Thank you 🙂
1. When making mRNA to DNA, we use reverse transcriptase. When the cDNA is made and we remove the mRNA by adding alkali. Is the complementary DNA strand now made using DNA Polymerase I or III?
2. In genetic engineering, when a recombinant dna enters a host cell, it either integrates, disintegrates or remains as an episome. Does the reason it disintegrates is because the host cell can detect it doesn’t have the same methylation sequence and cuts it via host controlled restriction??
3. In genetic engineering, when we want to clone a gene, I have taken in class that we don’t use PCR all the time because to use it, you have to know the sequence of the annealing sites. I don’t understand this because when you want to cut a plasmid to use as a vector, should we know the sequence anyway, to make sure we dont cut a gene or insert the foreign dna between a gene hat is important for the plasmid to actually work? For example, M13 phage has 10 genes and we shouldnt cut any of those genes otherwise we cant use it as a vector, right? So dont we know the sequence, so why cant we always use PCR?
I have a quiz coming up in 5 days and I was wondering if there are any good sites for solving questions about ligation, restriction endonuclease, blunt and sticky ends and pUC8 plasmids and whatnot. If you know any sites that have answers as well as questions please let me know otherwise I wont be able to know if I did it right or wrong. It is ok if the questions are multiple choice. I am looking for mostly questions where they give you sticky ends or the RE enzyme ad tell you if you can ligate it or how would you use it blah blah
Thanks for your time 🙂