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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 statements don’t hold true for the forensics and the amplification carried out?
2. If two successive PCRs are carried out, in which PCR there are chances of having a non-specific product?
3. What is the half life cycle for Taq polymerase?
4. A reaction mixture for PCR consists of ____________
5. PCR products can be analysed in many ways. Which of the following is not possible?
6. Errors can be introduced because of many reasons such as polymerase error or because of heterogeneity. Which of the statement holds true?
7. These are steps taken in carrying out the PCR reaction:
i) Attaching of primers by cooling
ii) Denaturation of strands
iii) DNA synthesis
iv) Heating
Which is the correct order?
(Mentioned from starting to ending the reaction)
8. An alternative to adding polymerase at later stage is __________
9. Both the primers, the start primer and the end primer should have a nearly same melting temperature.
10. Generally, amplification is carried out between the PCR primers. But if amplification is carried out outside the primers, it is called as __________
11. The process of amplification of specific DNA sequences by an enzymatic process is termed as ____________
12. Which of the following is useful in applications of PCR?
13. PCR is useful in population genetics because at times it can be used to study genetics of bacteria that can’t be cultured axenically.
14. If the template DNA belongs to several individual rather than single one, this type of heterogeneity is known as ____________
15. The primer annealing temperature is often very low from the maximum temperature. This low temperature leads to some mismatches.
16. There are basically two types of contamination, laboratory and external. If a PCR product is found to be contaminated by bacteria. It comes under laboratory contamination.
17. Which one of the following is not done if amplification of the non flanking region is carried out?
18. Primers and polymerases are added again during the reaction because they get consumed as the reaction proceeds.
19. By using two oligonucleotides, we can measure the amount of quantity of DNA by measuring the amount of fluorescence. The first probe absorbs light and the second emits it at a particular wavelength.
20. Which of the following statement is incorrect regarding the cloning of PCR products?
21. What will happen if the amino acid sequence is used directly for primer designing?
22. Which of the following is a characteristic of Taq polymerase?
23. If two successive PCR are carried out, it is called as __________
24. In another method of quantitative PCR, reporter-quencher set up is used. Which of the statement holds true for this methodology?
25. All the molecules generated during PCR will not be full length. Some will also be of intermediate length. Which of the statements is correct?