WORLD OF CELL+MASTERING ACCESS >CUSTOM
WORLD OF CELL+MASTERING ACCESS >CUSTOM
9th Edition
ISBN: 9781323445044
Author: Hardin
Publisher: PEARSON C
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Chapter 17, Problem 1Q

The theoretical amplification accomplished by n cycles of PCR is 2n. Starting from a single DNA segment, how much amplification would you expect to see after 20 cycles of PCR? After 30 cycles?

Expert Solution
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Summary Introduction

To determine: The amplification of a single DNA segment after 20 cycles of PCR.

Introduction: PCR, also known as, Polymerase Chain Reaction is a DNA amplification technique, which rapidly amplifies and separates DNA segments that are present in small amounts. PCR is used in DNA fingerprinting, DNA sequencing, and forensic sciences. Enzyme DNA polymerase is used in the process of PCR. The enzyme used is heat stable as PCR follows thermal cycling.

Explanation of Solution

The first step of PCR is to identify the DNA segment to be amplified. A single-stranded DNA primer complementary to the target segment is synthesized. Taq polymerase which is a thermostable DNA polymerase is added to catalyze the synthesis of the complementary DNA strand and various amplification cycles are performed to get the desired result.

The general formula for DNA amplification for n number of cycles is 2n.

The result of the amplification of a single segment after 20 cycles will be as follows:

220=1,048,576

Therefore, after 20 cycles a single DNA segment will be amplified to millions of copies.

Expert Solution
Check Mark
Summary Introduction

To determine: The amplification of a single DNA segment after 30 cycles of PCR.

Introduction: PCR, also known as, Polymerase Chain Reaction is a DNA amplification technique, which rapidly amplifies and separates DNA segments that are present in small amounts. PCR is used in DNA fingerprinting, DNA sequencing, and forensic sciences. Enzyme DNA polymerase is used in the process of PCR. The enzyme used is heat stable as PCR follows thermal cycling.

Explanation of Solution

PCR begins with the identification of the DNA segment to be amplified and is followed by the synthesis of a single-stranded artificial primer complementary to the DNA segment which needs to be amplified. DNA polymerase called Taq polymerase is then added to add nucleotide sequences and synthesize the complementary strand. This process is repeated over n number of cycles in order to achieve the desired results.

The amount of copies produced after n number of cycles is given by the formula 2n.

The result of the amplification of a single segment after 30 cycles will be as follows:

230=1,073,741,824

Therefore, after 30 cycles a single DNA segment will be amplified to billions of copies.

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Students have asked these similar questions
. In the PCR process, if we assume that each cycle takes5 minutes, how manyfold amplification would be accomplished in 1 hour?
Assuming that you start with one genome copy and are trying to amplify a 2000 bp DNA fragment, how many rounds of PCR do you need to do before you have products of the correct length?
PCR is an exponential copying of the template strands and can be represented by the function: y = a * 2n, where a is the initial number of template copies and n is equal to the number of cycles PCR has gone through.  How many DNA fragments would be produced after: 15 cycles? 13 cycles with 13 starting template strands? 29 cycles with 32 starting template strands?
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