A) DNA fingerprinting.
B) next-generation sequencing.
C) transgenic research.
D) reverse genetics.
E) positional cloning.
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A) Increase the amount of gene used.
B) Add linkers to generate new restriction enzyme sites.
C) Use a cosmid as a cloning vector.
D) Use dideoxy sequencing to obtain the sequence of the gene.
E) Cut the DNA with a blunt end cutter.
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A) one
B) two
C) three
D) four
E) one or two
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A) Add less Cas9 enzyme.
B) Create a longer sgRNA.
C) Try a different sgRNA that will still pair within the gene of interest.
D) Use separate crRNA and tracrRNA molecules.
E) Use a higher-fidelity version of Cas9.
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A) denaturation of the double-stranded template, extension of the new DNA molecules, primer annealing
B) denaturation of the double-stranded template, primer annealing, extension of the new DNA molecules
C) denaturation of the double-stranded template, extension of the new DNA molecules, hybridization of the template
D) degradation of the template, primer annealing, extension of the new DNA molecules
E) hybridization of the single-stranded templates, primer annealing, extension of the new DNA molecules
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A) can measure the amount of DNA amplified as the reaction proceeds, while standard PCR cannot.
B) can amplify DNA a billion-fold within just a few hours, while standard PCR cannot.
C) can determine the DNA sequence, while standard PCR cannot.
D) uses DNA polymerase, while standard PCR does not.
E) requires primers, while standard PCR does not.
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Multiple Choice
A) Genomic libraries contain fewer restriction enzyme sites, whereas cDNA libraries contain many more.
B) A genomic library is prepared from total genomic DNA, whereas a cDNA library is prepared from mRNA.
C) Genomic libraries contain much more sequence information and are much larger than cDNA libraries.
D) Genomic libraries contain coding and noncoding (regulatory, intron, etc.) sequences, whereas cDNA libraries contain only coding sequences along with their associated 5' and 3' untranslated regions.
E) cDNA libraries are generated with the use of reverse transcriptase, whereas genomic libraries are not.
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A) Bt toxin
B) G418
C) cleavage of X-gal
D) penicillin resistance
E) gancyclovir
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A) RNA polymerase.
B) DNA polymerase.
C) reverse transcriptase.
D) dNTPs.
E) mRNAs.
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A) EcoRII
B) PvuII
C) EcoRI
D) BglII
E) CofI
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A) plasmid
B) bacteriophage
C) agrobacterium
D) bacterial artificial chromosome
E) cosmid
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A) Ti plasmid
B) Agrobacterium tumefaciens
C) selectable markers
D) Ti plasmids and Agrobacterium tumefaciens only
E) Ti plasmids, Agrobacterium tumefaciens, and selectable markers
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Multiple Choice
A) 4, 2, 3, 5, 1, 6
B) 4, 5, 2, 3, 1, 6
C) 4, 2, 5, 1, 6, 3
D) 4, 3, 2, 5, 1, 6
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A) cDNA library
B) PCR library
C) genomic library
D) knockout library
E) transgenic library
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A) Forward genetics
B) Reverse genetics
C) Mutagenesis with radiation
D) CRISPR-Cas9 genome editing targeting the gene of interest followed by nonhomologous end joining (NHEJ)
E) CRISPR-Cas9 genome editing targeting the gene of interest followed by homologous recombination (HR) with a donor template
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A) DNA
B) RNA
C) protein
D) DNA and RNA
E) DNA, RNA, or protein
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Multiple Choice
A) He carried out step 2 at too low a temperature
B) He carried out step 2 at too high a temperature.
C) He designed primers with repetitive sequences.
D) He contaminated the template DNA sample.
E) He carried out step 3 for too short a time.
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