Q. Mutation is never deliberately induced in PCR products.

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Q. Choose the correct statement with regard to quantitative PCR?

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Q. By using two oligonucleotides, we can measure the amount of quantity of DNA by measuring the amount of fluorescence. The first probe absorbs light and the second emits it at a particular wavelength.

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Q. In another method of quantitative PCR, reporter-quencher set up is used. Which of the statement holds true for this methodology?

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Q. Which of the statement hold true for Quantitative PCR?

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Q. How many approaches are there for measuring the quantity of PCR products?

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Q. Which type of PCR allows the use of permeabilized tissue?

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Q. Reverse transciptase PCR is also carried out at times. Which of the statement is true?

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Q. Which one of the following is not done if amplification of the non flanking region is carried out?

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Q. Generally, amplification is carried out between the PCR primers. But if amplification is carried out outside the primers, it is called as __________

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Q. Topoisomerse I is also used for cloning of PCR product at times. Which of the statement holds true for such type of cloning?

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Q. Which of the following statement is incorrect regarding the cloning of PCR products?

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Q. How can PCR product be cloned into a vector?

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Q. The process of inserting an amplified PCR product in a vector for cloning is known as __________

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Q. If two successive PCRs are carried out, in which PCR there are chances of having a non-specific product?

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Q. If two successive PCR are carried out, it is called as __________

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Q. Touch-down PCR is another modification. Its characteristics include:

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Q. The primer annealing temperature is often very low from the maximum temperature. This low temperature leads to some mismatches.

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Q. An alternative to adding polymerase at later stage is __________

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Q. Hot-start PCR is a modification of PCR. Which of the following is not corresponding to it?

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