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What is the principle for selecting potential recombinant clones in molecular biology?
What is the principle for selecting potential recombinant clones in molecular biology?
Look for clones that have incorporated the desired DNA sequence. This can be done through PCR or DNA sequencing. The clone should contain the correct DNA fragment before further analysis. Selecting recombinant clones involves identifying bacteria that have successfully incorporated a plasmid with a gene of interest, achieved using antibiotic resistance markers.
How is the presence of genetically transformed cells confirmed in molecular cloning experiments?
How is the presence of genetically transformed cells confirmed in molecular cloning experiments?
The principle is to use antibiotic resistance markers. For example, if the plasmid confers ampicillin resistance (Ampr), only E. coli cells that have taken up this plasmid will grow on media containing ampicillin. This ensures that only genetically transformed cells are studied further.
What does the observation of growth on media containing ampicillin indicate in molecular cloning experiments?
What does the observation of growth on media containing ampicillin indicate in molecular cloning experiments?
It indicates viable cells and successful transformation. However, it does not confirm the presence of the specific gene of interest (GOI)-containing plasmid. Further steps are required to isolate and confirm the presence of the specific GOI-containing plasmid.
What is the significance of identifying bacteria that have successfully incorporated a plasmid with a gene of interest?
What is the significance of identifying bacteria that have successfully incorporated a plasmid with a gene of interest?
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What are potential methods for confirming the incorporation of the desired DNA sequence in recombinant clones?
What are potential methods for confirming the incorporation of the desired DNA sequence in recombinant clones?
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