हिंदी

Methodology for rDNA Technology

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Estimated time: 5 minutes
Maharashtra State Board: Class 12

Key Points: Methodology for rDNA Technology

  • The first step is isolation of DNA from the donor organism and cutting it into fragments using restriction enzymes.
  • The desired gene (foreign DNA) is selected and inserted into a cloning vector (like a plasmid) using DNA ligase to form recombinant DNA.
  • The recombinant DNA is transferred into a competent host cell (e.g., E. coli) by transformation or other methods like electroporation.
  • Transformed cells are identified using marker genes (e.g., antibiotic resistance) to distinguish them from non-transformed cells.
  • Selected transformed cells are multiplied in culture, leading to replication of recombinant DNA.
  • The inserted gene is expressed to produce the desired product, such as enzymes, hormones, or antibiotics.
  • Finally, the product is extracted and purified through downstream processing for use.
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