In the first gene cloning experiment:

1.  Researchers successfully identified a human gene responsible for the disease.
2.  Researchers successfully inserted a gene for kanamycin resistance into a plasmid vector.
3.  Researchers demonstrated that many different DNA fragments could insert into a plasmid vector
4.  Researchers produced a strain of bacteriophage with an increased ability to infect E. coli.

Subtopic:  Restriction Enzymes - Main Enzymes |

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Which of the following would NOT be a useful selectable marker?

1.  A gene encoding a protein that degrades the antibiotic ampicillin.
2.  A gene encoding a protein that allows the cell to synthesize histidine.
3.  A gene encoding a protein that is an essential structural component of the cell.
4.  All of these are useful selectable markers.
Subtopic:  Selectable Markers: I | Selectable Markers: II | Selectable Markers |
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Consider the following statements:

I:  Asexual reproduction preserves genetic information while sexual reproduction permits variations.
II:  Traditional hybridization often leads to the inclusion and multiplication of undesirable genes along with the desired genes.
III:  rDNA technology allows us to isolate and introduce only one or a set of desirable genes without introducing undesirable genes in the target organism.

Which of the above statements are true?

1. I and II only 2. I and III only
3. II and III only  4. I, II, and III
Subtopic:  Process of Biotech |
 83%
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Consider the following statements:

I:  Exonucleases remove nucleotides from the ends of DNA whereas, endonucleases make cuts at specific positions within DNA.
II:   To visualize pure DNA fragments, it is stained with ethidium bromide and seen in UV light.
III:  Plasmids and phage DNA are used as vectors in genetic engineering as they are extrachromosomal DNA molecules.

Which of the above statements are true?

1. I and II only 2. I and III only
3. II and III only  4. I, II, and III
Subtopic:  Tools: Enzymes: I | Tools |
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Consider the following statements: 

I:  Ori is responsible for the copy number of the linked DNA.
II:  Transformation is a process through which a piece of DNA is introduced into a host bacterium. 
III:  Bacteriophages have very high copy numbers of their genome within the bacterial cell.

Which of the above statements are true?

1.  I and II only 2.  I and III only
3.  II and III only  4.  I, II, and III
Subtopic:  Tools: Vectors: I | Selectable Markers: I | Selectable Markers | Tools |
 79%
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Consider the following statements:

I:  Biolistics or gene gun can be used to introduce genes in both plant and animal cells.
II:  Agrobacterium tumefaciens does not naturally infect Monocots.
III:  Liposomes are used in gene therapy for cystic fibrosis.

Which of the above statements are true?

1.  I and II only 2.  I and III only
3.  II and III only  4.  I, II, and III

Subtopic:  Host & Desired DNA: II | Host & Desired DNA |
 73%
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The bioreactor shown in the diagram is:
 

1. Sparged stirred tank type 2. Airlift type
3. Simple stirred tank type 4. Fluidized bed type
Subtopic:  Bioreactors/Downstream Processing |
 72%
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You are inserting your gene of interest into the Lac Z gene in a plasmid also containing a tetracycline-resistant gene. You plate your transformed bacteria on media containing tetracycline and X-gal. Which of the following results would indicate a clone with recombinant plasmids?

1.  A clone which did not grow on the tetracycline plates
2.  A white colony on the tetracycline plates
3.  A blue colony on the tetracycline plates
4.  A red colony on the tetracycline plates

Subtopic:  Selectable Markers: III | Selectable Markers |
 58%
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What type of probe would you use for a Western blot experiment?

1.A known DNA sequence.2.An RNA molecule.
3.A purified protein.4.An antibody.

Subtopic:  Process of Biotech |

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Which of the following is not part of the normal process of cloning recombinant DNA in bacteria?

1.  restriction endonuclease digestion of cellular and plasmid DNAs.
2.  production of recombinant DNA using DNA ligase and a mixture of digested cellular and plasmid DNAs.
3.  separation of recombinant DNAs by electrophoresis using the Southern technique to determine where the desired recombinant migrates.
4.  transformation of bacteria by the recombinant DNA plasmids and selection using ampicillin.
Subtopic:  Host & Desired DNA: II | Process of Biotech | Host & Desired DNA |
 53%
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