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AAB MOLECULAR DIAGNOSTICS FINAL PAPER 2026 COMPREHENSIVE SOLUTION COMPILATION

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AAB MOLECULAR DIAGNOSTICS FINAL PAPER 2026 COMPREHENSIVE SOLUTION COMPILATION

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AAB MOLECULAR DIAGNOSTICS FINAL
PAPER 2026 COMPREHENSIVE SOLUTION
COMPILATION

◉ What is a method for removing nucleotides and primers from PCR
products prior to sequencing?
Answer: Shrimp alkaline phosphatase (SAP) and exonuclease I
(ExoI)


◉ How does nested PCR increase both specificity and sensitivity?
Answer: By using two pairs of primers to amplify a single target in
two separate PCR runs. The second pair of primers bind slightly
inside the binding sites of the first pair. This will increase the
intended PCR product.


◉ How does PCR differ from qPCR (real time)?
Answer: PCR detects the final product by endpoint analysis.


◉ How does qPCR differ from PCR?
Answer: qPCR detects the quantity of product as it is produced
during the run.

, ◉ What is the purpose of the quencher in qPCR?
Answer: To reduce the florescence signal.


◉ What are three common molecular tests that involve the
amplification of probe sequences?
Answer: Ligase Chain Reaction (LCR), Strand Displacement
Amplification (SDA), and Q-beta Replicase.


◉ What is isothermal amplification?
Answer: A process that uses one temperature for amplification after
the initial denaturation.


◉ The major amplification products in Strand Displacement
Amplification (SDA) is?
Answer: Probes/Primers


◉ Strand Displacement Amplification (SDA) was first widely used to
detect which organism?
Answer: Mycobacterium tuberculosis


◉ Where does Q-beta Replicase derives its name?
Answer: From the major enzyme that is used to amplify the probe
sequence (Q-beta replicase)

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