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Genetic Engineering Practice Test: Polymerase Chain Reaction
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Polymerase Chain Reaction topics include: Primers, applications, precautions and drawbacks, basic techniques and modifications in PCR. Polymerase chain reaction (PCR) is a laboratory method that makes millions to billions of copies of a specific DNA sample. This allows scientists to study a very small sample of DNA in detail.  PCR is based on the principle of enzymatic replication of nucleic acids. It works by: Unzipping the DNA helix Using each strand as a template to build a new strand of DNA Repeating this process  PCR is used in whole genome sequencing and in genomic tests that... Show more
Genetic Engineering Practice Test: Polymerase Chain Reaction
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25 Questions

1. Which of the statement is correct for misincorporation?
2. The process of amplification of specific DNA sequences by an enzymatic process is termed as ____________
3. What are primers?
4. What is the correct statement with respect to ddNTPs?
5. Primers are generally ____________
6. In the case of uncertainty, if more than one nucleotide is included at a position it is called ____________
7. Choose the correct statement with regard to quantitative PCR?
8. Polymerases are also available from other Thermus species. Which of the following is correct?
9. If cytosine is deaminated, which of the base is formed?
10. Polymerases are available with proof reading activity. Which of the following are the characteristics of these types of polymerases?
11. Which of the following activity is not present in Taq polymerase?
12. What will happen if the amino acid sequence is used directly for primer designing?
13. Which of the statements don’t hold true for the forensics and the amplification carried out?
14. All the molecules generated during PCR will not be full length. Some will also be of intermediate length. Which of the statements is correct?
15. The process of inserting an amplified PCR product in a vector for cloning is known as __________
16. In another method of quantitative PCR, reporter-quencher set up is used. Which of the statement holds true for this methodology?
17. How many approaches are there for measuring the quantity of PCR products?
18. Reverse transciptase PCR is also carried out at times. Which of the statement is true?
19. Why internal secondary structures are not preferred for primers?
20. Which of the statement is incorrect for jumping PCR?
21. Topoisomerse I is also used for cloning of PCR product at times. Which of the statement holds true for such type of cloning?
22. Thermococcus litoralis grows at a temperature upto 98 degrees.
23. Primers and polymerases are added again during the reaction because they get consumed as the reaction proceeds.
24. Both the primers, the start primer and the end primer should have a nearly same melting temperature.
25. During amplification, there are chances of having a product of a mixture of different sequences. There are various ways to detect it. Which of the statement is true in regard to it?