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Molecular Biology Practice Test: Manipulation of Nucleic Acids & Polymerase Chain Reaction
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Avg score: 75% Most missed: “At what temperature do denaturation of DNA double helix takes place?”
Manipulation of Nucleic Acids & Polymerase Chain Reaction topics include: DNA manipulation, DNA and RNA hybridization, PCR fundamentals, inverse PCR, randomly amplified polymorphic DNA and reverse transcriptase PCR. The polymerase chain reaction (PCR) is a technique that can amplify a specific DNA sample to allow for detailed study. It is a fundamental technique in genetic testing and research, and is used in many medical laboratory applications.  PCR involves three main steps: Denaturation of dsDNA template at 92–95°C Annealing of primers at 50–70°C Extension of dsDNA... Show more
Molecular Biology Practice Test: Manipulation of Nucleic Acids & Polymerase Chain Reaction
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25 Questions

1. In case of northern blotting the hybridization occurs between two RNA molecules.
2. The temperature at which DNA synthesis takes place is 74˚C.
3. With respect to RAPD which of the following is false?
4. In how many ways a DNA can be labeled?
5. RAPDs can be used to detect multiple alleles of a marker.
6. The DNA concentration in inverse PCR is kept low.
7. At what temperature do annealing of DNA and primer takes place?
8. RAPDs are much more convenient markers than RFLPs.
9. The inheritance pattern of RAPD is _______________
10. Which is the most common organism considered for genetic manipulations?
11. At what temperature do denaturation of DNA double helix takes place?
12. Reverse transcriptase produces DNA from RNA.
13. Which of the following does not affect the formation of hybrid DNA?
14. Primer used for the process of polymerase chain reaction are ______________
15. Transformation does not involve ____________
16. RAPDs cannot be used for PCR amplification.
17. Why is a probe labeled?
18. Which of the following is an essential feature for being a perfect vector?
19. From which organism is the enzyme reverse transcriptase isolated?
20. How many primers are used in the process of reverse transcriptase amplification?
21. The vector and the DNA insert are cut by different enzymes for convenience.
22. Fluorescent labeling is an important phenomenon in case of hybridization and manipulations in molecular biology.
23. Annealing of primer is facilitated by complementary region.
24. With respect to target DNA used in inverted PCR which of the following is not true?
25. Which of the following is a mismatch?