I hate hole's class too!
Difference between real time PCR and reverse transcription PCR is as follows:- 1. Real time PCR is donated as qPCR and on the other hand reverse transcription PCR is denoted as RT-PCR. 2. In qPCR, the template used is single strand DNA strand whereas in the RT-PCR, the template used in process is single strand of RNA. 3. The real time PCR enables both quantification as well as detection of the DNA in the real time whereas the RT-PCR enables only the quantification of the RNA and it is little bit slower process then the qPCR as it first produce the cDNA from the template RNA strand and then process it in the similar fashion as the traditional PCR.
Some advantages are that it can create many copies of a minimal starting amount ie good for criminal investigations if you find some hair you can use PCR to find out whose it is. Also another advantage is PCR is speedy you can make tons of copies in hours. Disadvantages are that with PCR cannot substitute for gene cloning in cells when large amounts of a gene are desired. Also occasional errors during PCR replication impose limits on the number of good copies that can be made. source Campbell and Reece Biology 7th ed
to check is there any contamination in pcr products
It Inhibits the PCR reaction by chelating the magnesium ions.
Replication.
Polymerase Chain Reaction (PCR) involves DNA replication in a tube
The First discrete PCR product will be found in the 3rd round.
The PCR or Polymerase Chain Reaction is a laboratory system for DNA replication and amplificiation. It allows selected stretches of DNA to be duplicated using heat in the process.
Complementary base pairing
2x2x2=8 stranded DNA molecules
I hate hole's class too!
PCR need thermostable enzyme like taq DNA polymearse, while in replication using highly proofreading enzyme DNA polymerase. taq enzyme work in very high temprature while in replication our body temprature
replication
DNA replication duplicates the DNA strands. This process is accompanied by various enzymes such as DNA polymerase, Helicase, Topoisomerase.In labs they are constructred by Polymerase chain reaction(PCR).
types of pcr: AFLP -PCR. Allele-specific PCR. Alu-PCR. Assembly -PCR. Assemetric -PCR. Colony -PCR. Helicase dependent amplification. Hot start pCR. Inverse -PCR. Insitu -pCR. ISSR-PCR. RT-PCR(REVERSE TARNSCRIPTASE). REAL TIME -PCR
DNA cloning is where you take a piece of DNA and put it in a host cell so that every time the host cell replicates, its daughter cells will have that exact copy of DNA. DNA amplification is just taking a piece of DNA and making copies of it, like in the process of PCR. it is not inside a host cell. another way to think of it: you can amplify a gene--make a bunch of copies of it, and then clone it (by putting it in a cell and once that cell replicates each daughter cell has a copy of that DNA). you don't need to amplify anymore in cloning, you already did that before.