Regular PCR |
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Hot start PCR |
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High-Fidelity PCR |
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Immuno PCR. |
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Real-time PCR |
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2. The following information about Taq DNA polymerase is/are correct.
Taq DNA polymerase was discovered by Kary Mullis in 1983. |
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The entire Taq DNA polymerase reaction (PCR) technique was bought by Perkin Elmer in the range of $120 million. |
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Kary Mullis received a Nobel prize in 1993 for discovering Taq DNA polymerase. |
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Taq DNA polymerase was isolated from Thermus aquaticus. |
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It is a bacterial enzyme for DNA replication. |
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3. The following are true foe the specific PCR technique:
Tgo DNA Polymerase maintains four time the fidelity DNA amplification ib comparison to Taq DNA Polymerase. |
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High Fidelity PCR uses a combination of Taq DNA Polymerase and Tgo DNA Polymerase. |
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Tgo DNA Polymerase has 3’-5’ exonuclease or proofreading activity. |
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Long Template PCR system uses Taq DNA Polymerase and
thermostable DNA polymerase. |
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The error rate is decreased 30 folds by High Fidelity PCR in comparison toTaq DNA Polymerase. |
Question
2. The true statements about polymerase chain reaction are:
I. It is obtained from the Thermus aquaticus bacteria.
II. It is the bacterial enzyme used for DNA replication.
Hence option d, e are correct.
3. High Fidelity PCR uses the combination of Taq polymerase DNA and pfu. The high Fidelity PCR increases the rate of replication by 4 fold. Hence option b and e are correct.
Some of the PCR techniques for DNA amplification are: Regular PCR Hot start PCR High-Fidelity PCR...
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