
Phlebotomy Essentials
6th Edition
ISBN: 9781451194524
Author: Ruth McCall, Cathee M. Tankersley MT(ASCP)
Publisher: JONES+BARTLETT PUBLISHERS, INC.
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CGATTGCAGGTTATAGCG. Which of the following primer pair can be used to amplify this template with PCR?
a. GCTAA and TAGCG
b. GCTAA and CGCTA
c. CGATT and TAGCG
d: CGATT and CGCTA
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- This is from the Wilson et al. article.arrow_forwardThink about the function of the primers in a PCR that is designed to amplify a specific sequence, and about the temperatures of the PCR cycle. After considering these two points, give two reasons why 4-nucleotide long primers are not appropriate for PCR and explain.arrow_forwardRedraw Figure 10-6 with the goal of adding one EcoRIend and one XhoI end. Below is the Xhol recognitionsequence.Recognition sequence:. . . CTCGAG . . .. . . GAGCTC . . .After cut:. . . C TCGAG . . .. . . GAGCT C . . .arrow_forward
- a. What is the purpose of molecular cloning?b. What purpose do selectable markers serve in vectors?c. What is the purpose of the origin of replication in aplasmid vector?d. Why do cloning vectors have polylinkers?arrow_forwardWhat specifically will happen if DNA polymerase is inaccurate during DNA synthesis? Explain how this inaccuracy might affect the organism.arrow_forwardYou are performing a PCR reaction but unbeknownst to you, there is a significant pool of dUTP in the nucleotide mix (along with dCTP, dTTP, dATP, and dGTP). How might this affect your PCR product? a. If the PCR product was ligated into a plasmid and put into a cell, a totally different mRNA would be made from the insert compared to an insert made with T's. b. If the pool of dTTP ran out before the pool of dUTP, DNA replication could no longer occur. c. During the reaction, uracils incorporated into the product would cause the PCR product to degrade as it is being made. d. Uracil would be incorporated into the product and would lessen the affinity of any DNA binding proteins that might bind to the product in subsequent experiments. e. Nothing would happen since polymerases can't use dUTP to make DNA.arrow_forward
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