PCR MCQs: Polymerase Chain Reaction (PCR) is an important topic in Biotechnology - Principles and Processes for NEET Biology. This topic carries around 12% weightage in the NEET Biology syllabus. Understanding PCR MCQs is very important because multiple questions have been asked in NEET previous year question papers (PYQs) from this concept. Solving MCQs not only helps in revision but also improves speed and accuracy during the exam.
Practicing PCR MCQs will help you get a strong grip on this topic. You can also refer to NEET sample papers and chapter-wise weightage guides to know how often this topic is asked in exams.
PCR is a very important process in biotechnology that helps in DNA amplification. It is widely used in genetic testing, forensic science, and research. Many MCQs from this topic appear in NEET every year.
To understand PCR deeply and solve all related MCQs, you should read Biotechnology - Principles and Processes NEET notes. These notes cover all details needed to answer any NEET Biology MCQs related to PCR.
Free NEET PYQ PDF
PCR (Polymerase Chain Reaction) is a technique used to amplify a small DNA sample into millions of copies. It was developed by Kary Mullis in 1983. The process involves three main steps:
Denaturation: DNA strands are separated by heating.
Annealing: Primers attach to the DNA strands.
Extension: DNA polymerase adds new nucleotides to form new DNA strands.
PCR (Polymerase Chain Reaction) is widely used in medical diagnosis, forensic science, genetic engineering, and research.
The acronym PCR stands for Polymerase- Taq DNA polymerase plus chain- cyclic reaction plus response- biological activity. PCR stands for a polymerase chain reaction, which is controlled by Taq DNA polymerase. PCR is needed in almost every biotechnology process for the amplification and study of the DNA of various organisms. In this article, we will discuss some Frequently asked Multiple-choice questions in the NEET exam.Here are some important MCQs on PCR MCQs along with explanations.
the integration of natural science and organisms, cells, parts thereof, and molecular analogues for products and services.
techniques of using live organisms from organisms to produce products and processes useful to humans.
techniques of using enzymes from organisms to produce products useful to humans.
the techniques to alter the chemistry of genetic material (DNA and RNA).
Answer: A
Explanation: The European Federation of Biotechnology (EFB) defines biotechnology as a multidisciplinary field that integrates biology with technology to develop products and services.
II III
II III I
III II I
III I II
Answer: D
Explanation: The correct sequence for genetic modification involves first identifying the desired DNA, then introducing it into the host, and finally ensuring its maintenance and inheritance in the progeny.
Silver or Platinum
Platinum or Zinc
Silicon or Platinum
Gold or Tungsten
Answer: D
Explanation: Gold and tungsten are used to coat DNA in gene gun technology because they are non-reactive, dense, and can efficiently deliver genetic material into cells.
I and II only
I and III only
II and IV only
III and IV only
Answer: D
Explanation: The Roman numerals in restriction enzymes represent the order of discovery, not nucleotide sequence length. Also, restriction enzymes cut DNA, while methylases add methyl groups.
Both Statement I and Statement II are correct.
Statement I is correct but Statement II is incorrect.
Statement I is incorrect but Statement II is correct.
Both Statement I and Statement II are incorrect.
Answer: C
Explanation: Multiple recognition sites in a vector can complicate cloning. A vector should ideally have a single recognition site to facilitate precise gene insertion.
Statement I is correct but Statement II is incorrect.
Statement I is incorrect but Statement II is correct.
Both Statement I and Statement II are correct.
Both Statement I and Statement II are incorrect.
Answer: C
Explanation: Bioreactors are designed for optimal mixing of culture contents, and sampling ports allow small volumes to be withdrawn for monitoring without contaminating the system.
Exonuclease.
Endonuclease.
Hind-II.
EcoR I.
Answer: A
Explanation: Exonucleases remove nucleotides from the ends of DNA strands, whereas endonucleases cut at specific sequences within the DNA.
I only
II only
I and III only
II and IV only
Answer: B
Explanation: DNA fragments are negatively charged due to their phosphate backbone, not positively charged. Other statements about restriction enzymes and electrophoresis are correct.
PCR
Elution
DNA spooling
Electrophoresis
Answer: C
Explanation: The diagram likely represents electrophoresis, a technique used to separate DNA fragments based on size using an electric field.
Statement I is correct but Statement II is incorrect.
Statement I is incorrect but Statement II is correct.
Both Statement I and Statement II are correct.
Both Statement I and Statement II are incorrect.
Answer: C
Explanation: Bioprocess engineering ensures a sterile environment for cultures, and traditional hybridization can introduce unwanted traits, making selection complex.
Meloidogyne incognita
Bacillus thuringiensis
Agrobacterium tumefaciens
Escherichia coli
Answer: C
Explanation: This bacterium carries a natural Ti plasmid, which, after disarming, is used as a vector for transferring genes into dicot plant cells.
I and II only
I and III only
III and IV only
II, III and IV only
Answer: D
Explanation: DNA fragments are not visible under normal light without staining. However, agarose is derived from seaweed, the first recombinant DNA was created by Cohen and Boyer, and bacteriophages have high copy numbers.
Statement I is correct but Statement II is incorrect.
Statement I is incorrect but Statement II is correct.
Both Statement I and Statement II are correct.
Both Statement I and Statement II are incorrect.
Answer: D
Explanation: Restriction enzymes are derived from bacteria, not eukaryotes. The first discovered restriction enzyme was HindII, not EcoRI
They are oligonucleotides.
They are complementary to the regions of DNA.
They are helpful in annealing in PCR.
They are naturally obtained only.
Answer: D
Explanation: Primers are synthetic oligonucleotides used in PCR, not naturally occurring molecules.
In this, used medium is drained out from one side while fresh medium is added from other side.
In this cell are maintained in their physiologically most active lag phase of
Growth.
It produces larger biomass.
It shows higher yields of desired product.
Answer: B
Explanation: In a continuous culture system, cells are maintained in their log (exponential) phase, not lag phase, to maximize biomass and product yield.
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