Experience the power of community-driven knowledge on IDNLearn.com. Our platform is designed to provide accurate and comprehensive answers to any questions you may have.
Sagot :
There would be very little or no DNA produced if in a pcr reaction you used a dna polymerase isolated not from thermus aquaticus, but from an organism that grows at lower temperature .
What is the purpose of PCR?
To amplify (copy) a gene so it can be detected.
How do the strands separate during PCR?
- The hydrogen bonds between the two strands are broken by the DNA polymerase.
- During the annealing process, the primers split the strands. - The hydrogen bonds between the two strands are broken by the high heat of the denaturation stage.
What is a PCR test ?
- Targeting particular DNA fragments and amplifying (increasing in number) them artificially is done using the polymerase chain reaction technology. Describe how primers are used in PCR.
- The primer is a synthetic DNA strand that has bases that are complementary to the bases at the start of the DNA fragment that will be amplified.
Learn more about PCR
brainly.com/question/13052253
#SPJ4
We appreciate your participation in this forum. Keep exploring, asking questions, and sharing your insights with the community. Together, we can find the best solutions. Thank you for trusting IDNLearn.com with your questions. Visit us again for clear, concise, and accurate answers.
