Exam 7: Nucleic Acid Amplification

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Which of the following is a method of signal amplification?

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D

In PCR, an instrument is used to increase and decrease the temperature at set intervals as programmed by the technologist in order to:

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C

Real-time PCR differs from standard PCR in which way?

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A PCR assay is performed, and the results are being analyzed. The positive control has a band at the expected size; the negative template control has a band at the same size as the positive control; the contamination control has no band; and the amplification control has a band of expected size. All of the patient samples that were run had a band the same size as the band seen in the positive and negative template control wells. How are these results interpreted?

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Which of the following techniques is a primer-directed in vitro enzymatic reaction for the production of multiple copies of a specific DNA fragment found in a clinical sample?

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Which of the following is the most likely source of PCR contamination?

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A PCR reaction that uses more than one primer pair is called:

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Starting with a single target, how many copies are produced in a PCR reaction of 30 cycles?

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The specificity of the PCR reaction is determined by which of the following components?

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Which of the following PCR modifications was developed to allow for the amplification of an RNA template?

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Transcription-mediated amplification obtains:

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What is the purpose of an amplification control in PCR?

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Which modification of PCR uses short primers with random sequences that generate the amplification of many different products?

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Which of the following steps can be taken to minimize mis-priming in a PCR procedure?

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Which of the following is the function of SYBR Green in quantitative PCR?

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What is TaqMan?

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Nucleic acid has been isolated from a urethral swab and a PCR is performed on the sample to detect Neisseria gonorrhoeae. The positive control has a band at the expected size; the negative template control and the contamination controls do not have bands; and the amplification control has a band of expected size. The patient sample has a band consistent with the amplification control band and does not have a band corresponding to the positive control band. How is this result interpreted?

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Which of the following PCR controls ensures that the enzyme is active, the buffer is optimal, and the primers are priming the correct target sequence and must have a PCR product detected in order to be valid?

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TaqMan, molecular beacons, and scorpion-type primers are all used in which of the following procedures?

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What type of PCR starts with an RNA template?

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