Eliminating which of the following from a PCR reaction would result in no amplification of DNA?
a) template DNA
b) primers
c) Taq Polymerase
d) dNTPs
e) Eliminating any of these would result in no amplification of DNA
Eliminating which of the following from a PCR reaction would result in no amplification of DNA?...
Some of the PCR techniques for DNA amplification are: Regular PCR Hot start PCR High-Fidelity PCR Immuno PCR. Real-time PCR ------------------------------------ 2. The following information about Taq DNA polymerase is/are correct. Taq DNA polymerase was discovered by Kary Mullis in 1983. The entire Taq DNA polymerase reaction (PCR) technique was bought by Perkin Elmer in the range of $120 million. Kary Mullis received a Nobel prize in 1993 for discovering Taq DNA polymerase. Taq DNA polymerase was isolated from Thermus aquaticus....
25. Which is not a required reactant for a PCR reaction? Select one: a. Primer DNA b. Taq polymerase c. dNTP d. template DNA e. ATP
PCR utilizes specific DNA primers and polymerase enzyme to make copies of particular DNA sequence. The primers must attach to separated DNA at the target sequences so that the polymerase can build new DNA strands. What must also be added to the mixture besides primers and polymerase enzyme in order to get amplification and DNA? a. RNA polymerase b. dNTPs c. electron carriers d. DNA repair enzymes
You decide to use PCR to determine if your genotype for the PTC tasting gene TAS2R38. You then decide to also determine genotype for another gene called PER3. What PCR "ingredient" would be different in these two tests? Select one: a. Template gDNA b. dNTPS (nucleotides) c. Taq DNA polymerase d. Primers
a. List the six main components of a PCR amplification reaction and explain how its preseneel master mix is need for the production of an amplicon. Components Template DNA Primers MgCl2 dNTP Buffer Polymerase Why it is needed on
Select the components and equipment that would be necessary for doing PCR. select all that apply Sample containing the DNA to be amplified dNTPs (deoxyribonucleotide triphosphates) Taq polymerase (thermostable polymerase) RNA polymerase Restriction endonucleases Primers specific to the DNA sequence to be amplified Thermocycler
Which is not one of the elements needed to amplify DNA by polymerase chain reaction (PCR)? Question 16 options: A) Nucleoside triphosphates that serve as the source of the nucleotides A, T, C, and G needed in the synthesis of the new strands of DNA B) A restriction endonuclease enzyme that cleaves DNA at specific locations C) The segment of DNA that must be copied D) A DNA polymerase enzyme that will catalyze the synthesis of a complementary strand of...
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...
Which of the following molecules is not required for a PCR reaction? View Available Hint(s) Ligase O Primer O DNA O DNTPs Submit Previous Answers X Incorrect; Try Again; One attempt remaining dNTPs are required because they are the building blocks of DNA molecules. - Part B The thermostability of Taq polymerase is required during the annealing phase of PCR. View Available Hint(s) O True O False Submit
. Review your notes and the introduction for this lab regarding the components of PCR reactions. a. What is the function of primers in a PCR reaction? PCR primers is to provide a "free" 3'-OH group to which the DNA polymerase can add dNTPs b. What is the function of DNA polymerase in a PCR reaction? What specific DNA polymerase is used in PCR and why? c. What are nucleotides and what is the function of nucleotides in a PCR...