A) The target gene was not disrupted successfully.
B) Genes in addition to the target gene were disrupted.
C) The heterozygous mice in your cross did not mate properly.
D) The target gene is haploinsufficient; that is, a mutant phenotype is observed when only one copy of the gene is disrupted.
E) The target gene is essential for viability.
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A) origin of replication.
B) unique restriction enzyme sites.
C) Ti plasmid.
D) selectable markers.
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Multiple Choice
A) To date, there has not been a case of gene therapy curing a disease.
B) We have yet to develop a vector for delivering the gene.
C) Patients mount immune responses to the transferred gene and vectors.
D) We do not have the ability to use somatic gene therapy at this time.
E) We can only alter germ-line cells at this time.
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Multiple Choice
A) They have a gene of interest that has been fully disabled.
B) They have lower expression levels of a gene of interest.
C) They have higher expression levels of a gene of interest.
D) They have a point mutation in the gene of interest.
E) They have a gene removed, which results in lowered fertility.
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A) size.
B) electrical charge.
C) nucleotide content.
D) the probe used.
E) both size and electrical charge.
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Multiple Choice
A) siRNAs could be generated that would silence elevated levels of a harmful gene.
B) An RNAi library could be generated to assay harmful gene expression levels.
C) RNAi probes could bind to good genes and thus increase their expression.
D) RNAi could be used to amplify large amounts of therapeutic proteins.
E) RNAi cannot be used in humans, as it is a process found only in plants.
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Multiple Choice
A) A deletion of exon 24 in addition to exon 23
B) A deletion of intron 23
C) A deletion of 30 bases within exon 23
D) A deletion of 25 bases within exon 21
E) An insertion of a corrected copy of exon 23 after the mutant exon 23
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A) migrate more rapidly than
B) migrate at the same speed as
C) migrate more slowly than
D) cause degradation of
E) separate into
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A) one
B) two
C) three
D) four
E) one or two
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A) They act as primers for DNA polymerase.
B) They act as primers for reverse transcriptase.
C) They cut the sequenced DNA at specific sites.
D) They allow only the specific sequencing of the RNAs of a genome.
E) They stop synthesis at a specific site, so the base at that site can be determined.
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Multiple Choice
A) 1, 4, 5, 6, 2, 3
B) 4, 1, 6, 5, 3, 2
C) 4, 5, 1, 6, 2, 3
D) 1, 4, 5, 2, 6, 3
E) 1, 6, 4, 5, 2, 3
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A) Site-directed mutagenesis
B) Oligonucleotide-directed mutagenesis
C) CRISPR-Cas9 genome editing followed by nonhomologous end joining (NHEJ)
D) CRISPR-Cas9 genome editing followed by homologous recombination (HR) with a donor template
E) Mutagenesis with radiation
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A) E and H
B) S
C) X and N
D) S and N
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Multiple Choice
A) Coding sequences for gene products can be isolated from cDNA libraries.
B) Antibodies are used for Northern blot analysis.
C) The number of STR copies is variable throughout human populations.
D) PCR amplification generates large numbers of linear DNA fragments.
E) RNA molecules can be used as hybridization probes in Southern blot analysis.
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A) chromosome walking
B) DNA fingerprinting
C) site-directed mutagenesis
D) RNAi
E) CRISPR-Cas genome editing
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Multiple Choice
A) Selectable markers provide a means for preferentially allowing growth of only those bacterial cells that have been transformed with the cloning vector.
B) Unique restriction enzyme sites allow for larger pieces of foreign DNA to be inserted into the bacterial cloning vector.
C) Unique restriction enzyme sites provide a means for inserting the foreign DNA into the cloning vector at a specific known sequence site.
D) A bacterial origin of replication ensures that the plasmid is replicated while present within the bacterial cell.
E) Selectable markers provide a means for selecting cells that have been transformed with a recombinant plasmid.
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