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The difference between somatic cell gene therapy and germline therapy is that


A) germline therapy overcomes a protein malfunction in specific tissues but is not repaired in the entire organism and cannot be passed on to offspring.
B) somatic cell gene therapy is introduced into the egg, sperm or developing embryo, whereas germline therapy introduces a new gene into a mature tissue.
C) somatic cell gene therapy overcomes a protein malfunction in specific tissues but is not repaired in the entire organism and cannot be passed on to offspring.
D) germline therapy is the temporary repair of a genetic mutation, whereas somatic cell therapy is a permanent fix.

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The advantage of germline therapy over somatic cell therapy is that the normal gene is inserted into an egg,sperm,or developing embryo so that the repair is present in every cell of the organism as it matures to adulthood.

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The size of DNA is often given in the number of _____ that it contains.


A) genes
B) codons
C) base pairs
D) proteins
E) triplets

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DNA strands can begin to separate at the temperature of ______.


A) 37oC
B) 42oC
C) 60oC
D) 90oC
E) 100oC

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Which of the following is the second step in gene mapping?


A) Target DNA removed from cells and isolated
B) Cloning host treated with calcium chloride and receives plasmid
C) Separate DNA fragments with gel electrophoresis
D) Desired protein is produced by cloning host
E) Gene is amplified by multiplication of cloning host

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What type of DNA map is most detailed?


A) Linkage
B) Sequence
C) Physical
D) Geographical
E) Chromosomal

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Analysis of DNA fragments in gel electrophoresis is based on


A) larger fragments moving slowly and remaining closer to the wells.
B) DNA having an overall negative charge and moving to the positive pole.
C) DNA fragments being stained so that they can be seen.
D) application of an electric current through the gel causing DNA fragments to migrate.
E) All of the choices are correct.

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The various techniques by which scientists manipulate DNA in the lab are termed ______.


A) genetic engineering
B) biotechnology
C) recombinant DNA
D) gel electrophoresis
E) gene probes

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Common vectors used to transfer a piece of DNA into a cloning host are


A) plasmids.
B) viruses.
C) bacteriophages.
D) artificial chromosomes.
E) All of the choices are correct.

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When patient tissues are transfected with viruses carrying a needed,normal human gene,the technique is called ______.


A) cloning
B) gene therapy
C) antisense therapy
D) DNA fingerprinting

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Making new genomes is called ______.


A) bioengineering
B) synthetic biology
C) genetic engineering
D) cloning
E) recombinant DNA

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Two different nucleic acids can _____ by annealing at their complementary sites.


A) form a peptide bond
B) covalently bond
C) ligate
D) hybridize

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Gene probes can be labeled for detection with reporter molecules such as _____.


A) enzymes
B) fluorescent dyes
C) radioisotopes
D) All of the choices above can be used.

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The deliberate removal of genetic material from one organism and its subsequent transfer into the genome of another organism is a specific technique called ______.


A) genetic engineering
B) biotechnology
C) recombinant DNA technology
D) gel electrophoresis
E) gene probe technology

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Why is an enzyme from a thermophilic bacterium used in PCR?


A) The enzyme makes DNA that is more similar to human DNA.
B) This thermohile's enzyme will synthesize DNA.
C) DNA is replicated at a high temperature that denatures most proteins.
D) It is cheaper to obtain from live microorganisms than producing the enzyme in a lab.

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It is possible to identify mRNA molecules using fluorescently labeled cDNA.

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Amplification of DNA is accomplished by ______.


A) a Southern blot
B) a Western blot
C) DNA sequencing
D) gene probes
E) the polymerase chain reaction

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The field of pharmacogenomics uses knowledge of an individual's single nucleotide polymorphisms to determine how they will respond to a particular drug.

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The primers in PCR are


A) synthetic DNA oligonucleotides.
B) reverse transcriptases.
C) bacterial enzymes.
D) DNA polymerases.
E) short RNA strands.

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Which PCR step synthesizes complimentary DNA strands?


A) Heat target DNA to 94° C.
B) Add DNA polymerase and nucleotides at 72° C.
C) Repeat the cycle of heating and cooling.
D) Cool DNA to between 50° C and 65° C.
E) Add primers.

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