Answer:
After identifying a useful gene in
bacteria, following steps should be followed
(i) Isolation of useful gene using
restriction endonucleases
(li) Transferring the gene to a
suitable vector to create a recombinant DNA molecule
(iii) Transfer of these recombinant DNA
molecules to the target cells.
(iv) Screening of cells for
transformation
(v) Selection of transformed cells
(vi)
Regeneration of plants from the transformed cells to get transgenic plants.
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