A) digestive enzymes.
B) restriction enzymes.
C) enzymes from peroxisomes.
D) microscopic scalpels.
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A) reproductive cloning.
B) therapeutic cloning.
C) stem cell cloning.
D) gene therapy cloning.
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A) 1 - 1.5%
B) 5 - 7.5%
C) 9.5 - 15%
D) 34 - 55%
E) It changes during a person's life.
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A) structural DNA.
B) repeated sequences.
C) transposable elements.
D) exons.
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A) Thomson
B) Varmus
C) Wilmut
D) Spemann
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A) immune acceptance
B) shortened life span
C) intra-species transfer of specific genes
D) producing a viable vector
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A) the common cold.
B) cystic fibrosis.
C) tuberculosis.
D) anthrax.
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A) The vector used to carry the gene may elicit a strong immune response,leading to rejection of the added gene.
B) The virus vector may insert its DNA into the middle of a gene which could lead to cancer.
C) The genes carried by the virus vector could be used to produce more viruses.
D) All of the above.
E) The first two are correct.
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A) resistant to insect pests.
B) resistant to certain herbicides.
C) more nutritious.
D) All of these are correct.
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A) injecting mRNA for a protein into the roots of the plant.
B) inserting the Bt protein gene into the plant.
C) coating the plant with a gel that acts as a barrier.
D) All of these are correct.
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A) Because the individual's immune system is suppressed with drugs.
B) Because the cells are embryonic.
C) They are rejected,and that is why this has not worked yet.
D) Because the embryonic cells are cloned from the same individual they are injected into.
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A) adenovirus.
B) NIH virus.
C) rhino-associated virus.
D) adeno-associated virus.
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A) 3 billion
B) 500,000
C) About 25,000
D) 46
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A) amylase
B) peptidase
C) trypsin
D) ligase
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