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Most anticancer drugs such as the antimetabolites. alkalating agents and platinum based drugs target the S-phase of the cell cycle ( DNA replication/synthesis phase)

Other drugs like the antimicrotubules target the G2-M phase of the cell cycle

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Q: Where in the cell cycle could scientists target anticancer drugs?
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Explain why the precise length target DNA sequence doesn't get amplified until the third cycle?

In the first polymerization step, a new DNA strand is synthesized onto each primer. Taq polymerase extends this new strand well beyond the target sequence, producing a new DNA strand that contains the downstream/upstream primer and is longer than the target. In the second cycle, the DNA is denatured and primers anneal to the original target DNA and to the new DNA strands produced in the first cycle. A mixture of small target sequences and larger hybrid DNA sequences are produced at the end of the second cycle. In the third cycle, the target DNA of defined length is reprimed with both upstream and downstream primers. Taq polymerase then synthesizes two copies of target DNA of defined length. The number of these defined target sequences is doubled with each subsequent round of PCR, thereby increasing logarithmically. Thus, a 40 cycle PCR would amplify a given template 240 , thus potentially producing 1.0 x 1012 DNA molecules. In the first polymerization step, a new DNA strand is synthesized onto each primer. Taq polymerase extends this new strand well beyond the target sequence, producing a new DNA strand that contains the downstream/upstream primer and is longer than the target. In the second cycle, the DNA is denatured and primers anneal to the original target DNA and to the new DNA strands produced in the first cycle. A mixture of small target sequences and larger hybrid DNA sequences are produced at the end of the second cycle. In the third cycle, the target DNA of defined length is reprimed with both upstream and downstream primers. Taq polymerase then synthesizes two copies of target DNA of defined length. The number of these defined target sequences is doubled with each subsequent round of PCR, thereby increasing logarithmically. Thus, a 40 cycle PCR would amplify a given template 240 , thus potentially producing 1.0 x 1012 DNA molecules.


What questions might scientists have asked following the discovery of cyclin?

What is the function of a cyclin?How is cyclin expression regulates?Why do protein levels of the cyclins fluctuate throughout the cell cycle?


Wh of the following groups of scientists did NOT contribute to research in microbial genetics?

Winogradsky studied the microbial recycling of sulfur in the environment, while Beijerinck studied the nitrogen cycle in bacteria


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How soon after your menstrual cycle do you ovulate?

On average a woman ovulates 14 days after the first day of her period...however, everyone is different, so depending on the length of your cycle this could vary.

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Explain why the precise length target DNA sequence doesn't get amplified until the third cycle?

In the first polymerization step, a new DNA strand is synthesized onto each primer. Taq polymerase extends this new strand well beyond the target sequence, producing a new DNA strand that contains the downstream/upstream primer and is longer than the target. In the second cycle, the DNA is denatured and primers anneal to the original target DNA and to the new DNA strands produced in the first cycle. A mixture of small target sequences and larger hybrid DNA sequences are produced at the end of the second cycle. In the third cycle, the target DNA of defined length is reprimed with both upstream and downstream primers. Taq polymerase then synthesizes two copies of target DNA of defined length. The number of these defined target sequences is doubled with each subsequent round of PCR, thereby increasing logarithmically. Thus, a 40 cycle PCR would amplify a given template 240 , thus potentially producing 1.0 x 1012 DNA molecules. In the first polymerization step, a new DNA strand is synthesized onto each primer. Taq polymerase extends this new strand well beyond the target sequence, producing a new DNA strand that contains the downstream/upstream primer and is longer than the target. In the second cycle, the DNA is denatured and primers anneal to the original target DNA and to the new DNA strands produced in the first cycle. A mixture of small target sequences and larger hybrid DNA sequences are produced at the end of the second cycle. In the third cycle, the target DNA of defined length is reprimed with both upstream and downstream primers. Taq polymerase then synthesizes two copies of target DNA of defined length. The number of these defined target sequences is doubled with each subsequent round of PCR, thereby increasing logarithmically. Thus, a 40 cycle PCR would amplify a given template 240 , thus potentially producing 1.0 x 1012 DNA molecules.


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