Advertisements
Advertisements
प्रश्न
Describe three steps involved in mechanism of PCR.
Advertisements
उत्तर
At the start of PCR, all the requirements are mixed together in 'eppendorf tube' and the following operations are performed sequentially:
- Denaturation: The reaction mixture is heated to a temperature (90–98° C) to separate two strands of desired DNA. This is called denaturation.
- Annealing: The mixture is allowed to cool (40–60° C) that permits pairing of the primer to the complementary sequences in DNA. This step is called annealing.
- Primer extension/Polymerization: The temperature (70–75° C) allows thermostable Taq DNA polymerase to use single-stranded DNA as template and adds nucleotides. This is called primer extension. It takes around two minutes duration.
APPEARS IN
संबंधित प्रश्न
Retroviruses have no DNA. However, the DNA of the infected host cell does possess viral DNA. How is it possible?
Expand the following abbreviation: BAC
What are the restriction endonucleases? Give the rules of their nomenclature.
What is the cell that receives a recombinant gene called?
What is gene cloning? Explain different tools used for it.
The time taken to complete one cycle of PCR is around ______.
Study the following statements regarding separation of DNA using agarose gel electrophoresis.
- Large fragments of DNA molecules move faster than small DNA fragments and thus separate faster.
- DNA being negatively charged migrates to cathode.
Which one is a true statement regarding DNA polymerase used in PCR?
Name a recombinant vaccine that is currently being used in vaccination programme.
What is polymerase chain reaction (PCR)?
