NEET-UG Biology · Class 12
PCR and the steps of recombinant DNA technology — NEET & JEE Questions
PCR and the steps of recombinant DNA technology is a topic in Biotechnology: Principles and Processes, a Class 12 Biology chapter of the NEET-UG syllabus. TestBudy holds 17 published NEET-UG questions on PCR and the steps of recombinant DNA technology, each with the marking scheme of the real paper.
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PCR and the steps of recombinant DNA technology MCQs with solutions
10 of the 17 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.
PCR is primarily used to
- A. amplify a selected DNA sequence
- B. separate proteins by mass
- C. translate DNA into protein
- D. destroy all template DNA
Polymerase chain reaction (PCR) amplifies DNA following the equation.
- A.
- B.
- C.
- D.
During PCR, what happens during the annealing step?
- A. Restriction enzymes cut the amplified DNA
- B. DNA strands are separated by high temperature
- C. DNA polymerase synthesises new strands at maximum temperature
- D. Primers bind to complementary sequences on the template DNA
During PCR, the denaturation step mainly
- A. separates the two DNA strands
- B. allows primers to bind
- C. extends primers with DNA polymerase
- D. ligates vector and insert
Identify the correct sequence of steps in each cycle of Polymerase Chain Reaction :
- A. Extension â Annealing â Denaturation
- B. Annealing â Denaturation â Extension
- C. Denaturation â Extension â Annealing
- D. Denaturation â Annealing â Extension
Following are the steps involved in the process of PCR. A. Annealing B. Amplification (~1 billion times) C. Denaturation D. Treatment with Taq polymerase and deoxynucleotides E. Extension Choose the correct sequence of steps of PCR from the options given below :
- A.
- B.
- C.
- D.
Thermostable DNA polymerase used in PCR was isolated from :
- A. Thermus aquaticus
- B. Escherichia coli
- C. Agrobacterium tumifaciens
- D. Bacillus thuringiensis
Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R). Assertion (A) : Polymerase chain reaction is used in DNA amplification. Reason (R) : The ampicillin resistant gene is used as a selectable marker to check transformation. In the light of the above statements, choose the correct answer from the options given below :
- A. Both (A) and (R) are correct and (R) is the correct explanation of (A)
- B. Both (A) and (R) are correct but (R) is not the correct explanation of (A)
- C. (A) is correct but (R) is not correct
- D. (A) is not correct but (R) is correct
Match List-I with List-II . List-I List-II (a) Protpolast fusion (i) Totipotency (b) Plant tissue culture (ii) Pomato (c) Meristem culture (iii) Somaclones (d) Micropropagation (iv) Virus free plants Choose the correct answer from the options given below.
- A. (a) (b) (c) (d) (iv) (iii) (ii) (i)
- B. (a) (b) (c) (d) (iii) (iv) (ii) (i)
- C. (a) (b) (c) (d) (ii) (i) (iv) (iii)
- D. (a) (b) (c) (d) (iii) (iv) (i) (ii)
Which of the following is not an application of PCR (Polymerase Chain Reaction)?
- A. Detection of gene mutation
- B. Molecular diagnosis
- C. Gene amplification
- D. Purification of isolated protein
Common mistakes in PCR and the steps of recombinant DNA technology
Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.
- Putting downstream processing before recombinant DNA has been created and expressed.
- Places annealing before template strand separation.
- Assumes any DNA polymerase tolerates repeated near-boiling temperatures.
- Assumes DNA polymerase can initiate synthesis de novo at any desired target.
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