Plasmids are good cloning vectors mainly because:
 
1. they are circular
2. they replicate autonomously
3. they are extra-chromosomal DNA molecules found in many bacterial cells
4. they carry genes vital for normal survival and reproduction

Subtopic:  Tools: Vectors: I |
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In a plasmid such as pBR322:
I: Ori controls the copy number of DNA per cell
II: Multiple cloning sites are recognition sequences of common restriction enzymes
III: Genes for antibiotic resistance are used as selectable markers
 
1. Only I and II are correct
2. Only I and III are correct
3. Only II and III are correct
4. I, II, and III are correct
Subtopic:  Cloning Vector |
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A plasmid has genes for resistance against ampicillin and tetracycline. The tetracycline resistant gene is insertionally inactivated by inserting a foreign DNA within the gene. The bacterial cells are transformed. The recombinant transformants:
1. will be killed in a medium containing ampicillin but not in a medium containing tetracycline
2. will be killed in a medium containing tetracycline but not in a medium containing ampicillin
3. will be killed in a medium containing ampicillin and in a medium containing tetracycline
4. will not be killed in a medium containing ampicillin and in a medium containing tetracycline
Subtopic:  Cloning Vector |
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In agar gel electrophoresis, the restriction fragments produced by restriction enzymes:

1. move towards cathode
2. do not move at all
3. are separated according to size with smaller fragments moving farther
4. are transported onto a nitrocellulose membrane
Subtopic:  Separation and Isolation of DNA fragments |
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DNA can be visualized through UV rays if it is stained with:

 
1. Ethidium bromide 2. Polyethylene glycol
3. Tritiated thymidine 4. Colchicine

Subtopic:  Separation and Isolation of DNA fragments |
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The Ti Plasmid [ having T-DNA] is considered a natural genetic engineer and can transform:
1. bacterial cells
2. dicot plant cells
3. monocot plant cells
4. animal cells
Subtopic:  Cloning Vector |
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Normally, microinjection and biolistics [gene gun] are used, respectively, to transform:
1. plant cells and animal cells
2. animal cells and plant cells
3. animal cells and bacterial cells
4. plant cells and bacterial cells
Subtopic:  Transforming Plant & Animal Cell |
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It is usually necessary to induce ‘competence’ in bacterial cells to transform them in recombinant DNA procedures mainly because:
1. bacterial cell has a cell wall
2. bacteria do not have a well defined nucleus and membrane bound organelles
3. DNA is a hydrophilic molecule
4. DNA is associated with positively charged histone proteins

 
Subtopic:  Tools |
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It is possible to make human proteins in bacterial cells with rDNA experiments because:
1. bacterial cells replicate faster than eukaryotic cells
2. genetic code is almost universal
3. bacterial cells have plasmids that can be used as a vector
4. bacterial cells produce restriction enzymes

 
Subtopic:  General Design of an rDNA experiment |
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Polymerase chain reaction can amplify DNA, producing about 1 billion copies in 30 cycles. The correct sequence of the steps of this reaction is:
1. Denaturation → Annealing of primers → Extension of primers
2. Denaturation → Extension of primers → Annealing of primers
3. Extension of primers → Annealing of primers → Denaturation
4. Annealing of primers → Extension of primers → Denaturation
Subtopic:  Polymerase Chain Reaction: PCR |
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