A) linkage mapping.
B) linkage disequilibrium mapping.
C) candidate gene approach.
D) all of the above
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A) Southern blotting
B) in situ hybridization
C) PCR
D) Southern blotting and PCR
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A) origin of replication
B) drug-resistance gene
C) polylinker sequence
D) all of the above
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A) single-nucleotide polymorphisms.
B) nucleotide tandem replacements.
C) short tandem repeats.
D) autosomal dominant polymorphism.
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A) missense mutation.
B) nonsense mutation.
C) silent mutation.
D) none of the above.
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A) genomic DNA was present.
B) retroviral DNA was a contaminant.
C) endonucleases should have been added.
D) RNA polymerase was present.
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A) the cellular and tissue-specific localization of the mRNA encoded by a particular gene.
B) the activity of the protein translated from a particular mRNA.
C) the size of the mRNA transcript.
D) all of the above
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A) DNA denaturation,primer elongation,primer annealing
B) primer annealing,DNA ligation,primer elongation
C) primer elongation,primer annealing,DNA ligation
D) DNA denaturation,primer annealing,primer elongation
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A) 7.5 × 10² base pairs
B) 7.5 × 10³ base pairs
C) 7.5 × 10⁴ base pairs
D) 7.5 × 10⁵ base pairs
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A) disrupts the target DNA sequence.
B) results in the destruction of the target mRNA.
C) destroys the target protein.
D) all of the above
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A) resistant to G418 and resistant to ganciclovir.
B) sensitive to G418 and resistant to ganciclovir.
C) resistant to G418 and sensitive to ganciclovir.
D) sensitive to G418 and sensitive to ganciclovir.
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A) temperature-sensitive mutation.
B) recessive mutation.
C) conditional mutation.
D) suppressor mutation.
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A) determine if the cells are also making β-galactosidase
B) tag the protein with green fluorescent protein to see if it is degraded by G418
C) label a fragment of the gene to see where it is expressed
D) clone the gene into a G418-sensitive cell line,then treat these cells with G418
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A) epitope tagging.
B) in situ hybridization.
C) polymerase chain reaction.
D) next-generation sequencing.
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A) facilitate transfer of the cDNA into the E.coli cells.
B) provide a promoter for the transcription of the cDNA in E.coli.
C) facilitate purification of the expressed protein though binding to an affinity column containing chelated nickel atoms.
D) prevent degradation of the expressed protein by E.coli proteases.
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A) Tay-Sachs disease
B) Duchenne muscular dystrophy
C) cystic fibrosis
D) none of the above
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A) more than one genome.
B) more than two copies of each chromosome.
C) only one copy of each chromosome.
D) multiple copies of a specific chromosome.
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