Biotechnology Applications: PCR, Cloning, Recombinant DNA

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This category focuses on the core techniques of modern biotechnology that enable the analysis, modification, and amplification of genetic material. It covers PCR, cloning, and recombinant DNA technology, which form the foundation of genetic engineering, medical biotechnology, and molecular research. This section is suitable for Class 11–12 students, NEET aspirants, and undergraduate learners.

In this section, you will study:

  • Principles and steps of Polymerase Chain Reaction (PCR)

  • Enzymes, vectors, and host systems used in cloning

  • Steps involved in recombinant DNA technology

  • Restriction enzymes, ligases, and cloning vectors

  • Gene insertion, expression, and selection of recombinants

  • Applications of PCR and recombinant DNA in medicine, agriculture, and research

  • NCERT-based explanations, diagrams, flowcharts, MCQs, and exam-oriented questions

The content is structured to build clear conceptual understanding, strengthen process-based reasoning, and help students perform confidently in school examinations, NEET, and undergraduate assessments.

Develop a strong understanding of how molecular tools like PCR and recombinant DNA technology are applied to solve real-world biological problems.

Q. In recombinant DNA technology, what is the role of a vector?
  • A. To cut DNA
  • B. To amplify RNA
  • C. To transport DNA into a host cell
  • D. To visualize proteins
Q. What is the main purpose of cloning in biotechnology?
  • A. To create genetically identical copies of an organism
  • B. To sequence the entire genome
  • C. To mutate genes
  • D. To analyze gene expression
Q. What is the primary purpose of PCR (Polymerase Chain Reaction)?
  • A. To sequence DNA
  • B. To amplify DNA
  • C. To cut DNA
  • D. To visualize DNA
Q. What is the significance of the 'sticky ends' created by restriction enzymes?
  • A. They stabilize RNA
  • B. They allow for the easy joining of DNA fragments
  • C. They prevent mutations
  • D. They enhance PCR efficiency
Q. What type of mutation results in a change in a single nucleotide?
  • A. Frameshift mutation
  • B. Point mutation
  • C. Deletion mutation
  • D. Insertion mutation
Q. Which enzyme is primarily responsible for synthesizing new DNA strands during PCR?
  • A. DNA ligase
  • B. Taq polymerase
  • C. Restriction enzyme
  • D. RNA polymerase
Q. Which of the following techniques is used to separate DNA fragments by size?
  • A. PCR
  • B. Gel electrophoresis
  • C. Cloning
  • D. DNA sequencing
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