A) It has not been approved for use in the United States.
B) It degrades so easily that it has to be applied repeatedly.
C) It is not very toxic.
D) It is new and untested.
E) None of the above
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A) collection.
B) library.
C) museum.
D) bank.
E) farm.
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A) constructing a gene library.
B) constructing an expression vector.
C) performing a restriction digestion.
D) attempting to "silence" a gene.
E) constructing a recombinant plasmid.
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A) ligation reactions with blunt-end DNA molecules.
B) hybridization between DNA and transcription factors.
C) restriction endonucleases for cutting cell walls.
D) synthesizing cDNA molecules from mRNA templates.
E) the transcriptional activation of expression vectors.
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A) predict who will get cancer.
B) show transcriptional patterns in an organism during different times of development.
C) clone DNA.
D) make transgenic plants.
E) inhibit transcription of disease genes.
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A) Selective breeding to produce cows with greater milk yield
B) Pharming
C) Use of microbes to produce an antibiotic
D) The synthetic production of nylon using organic chemistry techniques
E) All of the above are examples of biotechnology.
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A) RNAi can be used with DNA chips.
B) Only RNAi can be used to test cause-and-effect relationships.
C) RNAi is more stable than antisense RNA.
D) RNAi is single-stranded and thus easier to produce.
E) None of the above
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A) Primary structure of the protein and the genetic code
B) Primary structure and secondary structure of the protein and the genetic code
C) Primary structure of the protein, the genetic code, promoter sequence, and codon usage
D) Secondary structure of the protein, the genetic code, and promoter sequence
E) Primary structure of the protein and promoter sequence
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A) PCR.
B) recombinant DNA.
C) complementary DNA.
D) DNA fingerprinting.
E) None of the above
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A) DNA ligase
B) DNA polymerase
C) RNA polymerase
D) Reverse transcriptase
E) Replicase
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A) separate proteins based on size and charge.
B) knock out a gene.
C) create antisense DNA.
D) measure expression levels of a gene.
E) coax DNA into host cells.
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A) RNAi
B) Knockout technology
C) Antisense
D) Mutant tRNA
E) Transposon mutagenesis
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A) single stranded.
B) not made in vivo.
C) relatively stable in cells.
D) capable of binding to specific mRNAs.
E) Both c and d
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A) bacterial plasmids.
B) viruses.
C) plant plasmids.
D) bacteriophage .
E) All of the above
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A) The analysis of traits determined by multiple genes
B) Overexpression of a particular gene
C) Silencing a particular gene
D) Knocking out a particular gene
E) Targeting a protein to the nucleus
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