The enzymes which are absolutely necessary for recombinant $DNA$ technology are

  • A
    restriction endonucleases and topoisomerases
  • B
    endonucleases and polymerases
  • C
    restriction endonucleases and ligases
  • D
    peptidases and ligases

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Similar Questions

Insertion of a foreign $DNA$ at $BamHI$ site in an $E. coli$ cloning vector $pBR322$ results in the loss of antibiotic resistance towards :

Which of the following would not be used in preparing recombinant $DNA$?

Restriction enzymes that are used in the construction of recombinant $DNA$ are endonucleases which cut the $DNA$ at 'specific-recognition sequence'. What would be the disadvantage if they do not cut the $DNA$ at specific-recognition sequence?

How many recognition sites are present for each restriction enzyme in the cloning vector $pBR322$?

Which of the following key factors makes a plasmid a suitable vector in genetic engineering?

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