Homework Answers
a. PCR primers are use to provide a "free" 3'-OH to which DNA polymerase can start adding dNTPs.
b. The role of DNA polymerase in PCR is same as in DNA replication which is to add nucleotides according to template strand.
The name of the specific DNA polymerase in PCR is Taq polymerase.
Taq polymerase is used in DNA replication because it can withstand the high temperature of PCR procedure.
c. Nucleotides are the units of nucleic acid, DNA and RNA.
The polymerization of nucleotides can form new DNA strand. The nucleotide Tri-Phosphate can supply energy for the polymerization process.
d. The overall goal of the PCR is to produce huge number of DNA (gene) copy in vitro which is known as gene cloning.
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. Review your notes and the introduction for this lab regarding the components of PCR reactions....
Lab 1 - PCR Pre-lab discussion. Discuss the following among your table prior to beginning the...
Lab 1 - PCR Pre-lab discussion. Discuss the following among your table prior to beginning the lab. 1. Describe the overall goal of the polymerase chain reaction. 2. List the components that are required for a PCR reaction. 3. A special DNA polymerase called Taq is used in PCR. What is unique about this enzyme and why is it used in the PCR reaction? 4. We will be using genomic DNA as our template DNA in this PCR reaction. How...
Now. you should be able to answer the following questions: • How the amplification will be...
Now. you should be able to answer the following questions: • How the amplification will be done? - How you will determine your target sequence? How the amplification will be specific for certain segment? What are the requirements to carry PCR? • Suppose you perform a PCR that begins with one double-strand of the following DNA template: +5'-CTACCTGCGGGTTGACTGCTACCTTCCCGGGATGCCCAAAATTCTCGAG-3+ +3'-GATGGACGCCCAACTGACGATGGAAGGGCCCTACGGGTTTTAAGAGCTC-5'+ A. Draw one cycle of PCR reaction below the following diagram. B. Label the template DNA, the primers, and what is...
Why do we want/need the presence of Mg2+ in a PCR but do not want it...
Why do we want/need the presence of Mg2+ in a PCR but do not want it present at all other steps of processing/analyzing a DNA sample? (2 marks) Identify and explain what generally occurs in each of the 3 main steps of a polymerase chain reaction. (6 marks) 8. Identify and explain what the 3 different PCR controls inform you about the results of a PCR. (3 marks) Highlight the 2 advantages and 3 disadvantages of using PCR. Ensure to...
Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain...
Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain reaction? a. To repair damaged DNA b. To make copies of entire chromosomes c. To make copies of specific regions of DNA d. To prepare cells for cell division 2. The polymerase chain reaction is most comparable to what cellular process? a. Mitosis b. Replication c. Transcription d. Translation 3. When enzymes are elongating (building) a newly synthesized DNA strand in PCR, new nucleotides...
CALCULATIONS [2 points each] You are asked to perform a PCR experiment in the lab. However, in th...
CALCULATIONS [2 points each] You are asked to perform a PCR experiment in the lab. However, in this experiment you must add each ingredient separately (unlike the "master-mix" we used in our own experiment). In this experiment, each PCR reaction tube contained the following ingredients added with a micropipetor... 10 HL of 5x Buffer 6 μ1 of 25 mM MgCl2 solution μL of 10 mM dNTP mix 1.5 μL oligonucleotide primer mix 0.5 HL Taq DNA Polymerase stock solution 28...
I need help to construct this lab report ... I need a well explained introduction and...
I need help to construct this lab report ... I need a well explained introduction and basics methods. ******* PLEASE DO NOT RESPOND IF YOU DONT HAVE THE INFORMATION I NEED*********** INTRODUCTION Introduce the overall idea behind our lab experiments using buccal cells 1. Real time PCR, using SYBR Green dye 2. Genotype DNA SNP (warrior-worrier gene) 3. Genotype DNA for SNP (ACTN3 gene) METHODS Isolation and dilution of DNA: summarize the method used to extract and dilute your gDNA....
8. PCR is used to. A Diagnose genetic disease 8 Solve cnmes C Sudy gene unction...
8. PCR is used to. A Diagnose genetic disease 8 Solve cnmes C Sudy gene unction D. All of th C ONA as a template to form RINA D All of the above 7. PCR technique does not need A. Tag polymerase B Restriion encymes C Olgoucletide prmers C. A fragment of skin D. All of the above 9 PCR can be used in A Cloning B.Sequening C.Medical dagnosis&foric mine 0.PCR can make mullple copies ot A. DNA B RNA...
Your lab instructor has given you a protocol to perform a molecular cloning experiment. In a...
Your lab instructor has given you a protocol to perform a molecular cloning experiment. In a previous experiment, you used polymerase chain reaction (PCR) to amplify a sequence that you believe to regulate expression of a gene you are studying. You will now take this purified PCR product (double stranded DNA) and ligate it into a plasmid that contains a luciferase reporter gene. If your DNA sequence is a promoter sequence, then its presence will allow for expression of the...
Draw (or arrange) only the items you need from the Lab Materials Page (picture below) in...
Draw (or arrange) only the items you need from
the Lab Materials Page (picture below) in the
order you would use them to make AND screen a gene library.
You will ‘draw’ the steps that use the Lab Materials in the correct
order to create and screen a gene library which has the assigned
gene clone. You will need to add some connecting words and phrases
to make all the steps for making your library clear.
The genomic gene clone...
Question: I need help to construct this I need help to construct this lab report ... I need a wel...
Question: I need help to construct this I need help to construct this lab report ... I need a well explained introduction and basics methods. ******* PLEASE DO NOT RESPOND IF YOU DONT HAVE THE INFORMATION I NEED*********** INTRODUCTION Introduce the overall idea behind our lab experiments using buccal cells 1. Real time PCR, using SYBR Green I dye 2. Genotype DNA SNP (warrior-worrier gene) 3. Genotype DNA for SNP (ACTN3 gene) METHODS 1. Isolation and dilution of DNA: summarize...
Lab 1 - PCR Pre-lab discussion. Discuss the following among your table prior to beginning the lab. 1. Describe the overall goal of the polymerase chain reaction. 2. List the components that are required for a PCR reaction. 3. A special DNA polymerase called Taq is used in PCR. What is unique about this enzyme and why is it used in the PCR reaction? 4. We will be using genomic DNA as our template DNA in this PCR reaction. How...
Now. you should be able to answer the following questions: • How the amplification will be done? - How you will determine your target sequence? How the amplification will be specific for certain segment? What are the requirements to carry PCR? • Suppose you perform a PCR that begins with one double-strand of the following DNA template: +5'-CTACCTGCGGGTTGACTGCTACCTTCCCGGGATGCCCAAAATTCTCGAG-3+ +3'-GATGGACGCCCAACTGACGATGGAAGGGCCCTACGGGTTTTAAGAGCTC-5'+ A. Draw one cycle of PCR reaction below the following diagram. B. Label the template DNA, the primers, and what is...
Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain reaction? a. To repair damaged DNA b. To make copies of entire chromosomes c. To make copies of specific regions of DNA d. To prepare cells for cell division 2. The polymerase chain reaction is most comparable to what cellular process? a. Mitosis b. Replication c. Transcription d. Translation 3. When enzymes are elongating (building) a newly synthesized DNA strand in PCR, new nucleotides...
CALCULATIONS [2 points each] You are asked to perform a PCR experiment in the lab. However, in this experiment you must add each ingredient separately (unlike the "master-mix" we used in our own experiment). In this experiment, each PCR reaction tube contained the following ingredients added with a micropipetor... 10 HL of 5x Buffer 6 μ1 of 25 mM MgCl2 solution μL of 10 mM dNTP mix 1.5 μL oligonucleotide primer mix 0.5 HL Taq DNA Polymerase stock solution 28...
8. PCR is used to. A Diagnose genetic disease 8 Solve cnmes C Sudy gene unction D. All of th C ONA as a template to form RINA D All of the above 7. PCR technique does not need A. Tag polymerase B Restriion encymes C Olgoucletide prmers C. A fragment of skin D. All of the above 9 PCR can be used in A Cloning B.Sequening C.Medical dagnosis&foric mine 0.PCR can make mullple copies ot A. DNA B RNA...
Draw (or arrange) only the items you need from
the Lab Materials Page (picture below) in the
order you would use them to make AND screen a gene library.
You will ‘draw’ the steps that use the Lab Materials in the correct
order to create and screen a gene library which has the assigned
gene clone. You will need to add some connecting words and phrases
to make all the steps for making your library clear.
The genomic gene clone...
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