Visual Essentials of Anatomy &Physiology
1st Edition
ISBN: 9780321780775
Author: Martini, Frederic
Publisher: Prentice Hall
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Chapter 8.1, Problem 1.8SR
Summary Introduction
To label: The cranial nerves and to indicate whether they carry out motor, sensory, or both the functions.
Introduction: The twelve pairs of cranial nerves are components of the peripheral nervous system. These nerves are numbered from I to XII. These nerves directly emerge from the brain and pass through distinct openings present in the cranium.
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a) Calculating Transformation Efficiency
For the +DNA/+Amp/+IPTG plate, record the following:
Number of transformants (colonies): _________________
Nanograms of plasmid DNA added: 50 ng
Final recovery volume: 0.50 mL
Volume plated: 0.25 mL
Transformation efficiency equation:
Transformation efficiency = Number of transformants / µg of DNA x Final volume at recovery (mL)/ volume plated (mL)
b) Using the equation above, calculate the transformation efficiency.
c) Describe the success of the transformation efficiency of this demo based on the calculation you did above?
a) What differences would you expect to see between the -DNA/+Amp and +DNA/+Amp plates?
b) Predict the growth you would expect to see on each of the following plates:
– DNA ___________________________________________________________
– DNA/+Amp ______________________________________________________
+DNA/+Amp ______________________________________________________
+DNA/+Amp/+IPTG _________________________________________________
1)Which plate did you see purple/pink/blue bacterial cells? Why did you see this growth? Explain your answer in terms of transformation and plasmids?
2) Calculating Transformation Efficiency
For the +DNA/+Amp/+IPTG plate, record the following:
Number of transformants (colonies): _________________
Nanograms of plasmid DNA added: 50 ng
Final recovery volume: 0.50 mL
Volume plated: 0.25 mL
Transformation efficiency equation:
Transformation efficiency = Number of transformants / µg of DNA x Final volume at recovery (mL)/ volume plated (mL)
3) Using the equation above, calculate the transformation efficiency.
4) Describe the success of the transformation efficiency of this demo based on the calculation you did above?
Chapter 8 Solutions
Visual Essentials of Anatomy &Physiology
Ch. 8.1 - Prob. 1LOCh. 8.1 - Prob. 2LOCh. 8.1 - Prob. 3LOCh. 8.1 - Prob. 4LOCh. 8.1 - Prob. 5LOCh. 8.1 - Prob. 6LOCh. 8.1 - Prob. 7LOCh. 8.1 - Prob. 1.1RCh. 8.1 - Prob. 1.2RCh. 8.1 - Prob. 1.3R
Ch. 8.1 - Identify the cranial nerves by name and number.
Ch. 8.1 - Prob. 2.2RCh. 8.1 - Prob. 2.3RCh. 8.1 - Prob. 3.1RCh. 8.1 - Prob. 3.2RCh. 8.1 - Prob. 3.3RCh. 8.1 - Prob. 4.1RCh. 8.1 - Prob. 4.2RCh. 8.1 - Prob. 4.3RCh. 8.1 - Prob. 5.1RCh. 8.1 - Prob. 5.2RCh. 8.1 - Prob. 5.3RCh. 8.1 - Prob. 6.1RCh. 8.1 - Prob. 6.2RCh. 8.1 - Prob. 6.3RCh. 8.1 - Prob. 7.1RCh. 8.1 - Prob. 7.2RCh. 8.1 - Prob. 7.3RCh. 8.1 - Prob. 1.1SRCh. 8.1 - Prob. 1.2SRCh. 8.1 - Prob. 1.3SRCh. 8.1 - Prob. 1.4SRCh. 8.1 - Prob. 1.5SRCh. 8.1 - Prob. 1.6SRCh. 8.1 - Prob. 1.7SRCh. 8.1 - Prob. 1.8SRCh. 8.1 - Prob. 1.9SRCh. 8.1 - Prob. 1.10SRCh. 8.1 - Prob. 1.11SRCh. 8.1 - Prob. 1.12SRCh. 8.1 - Label the indicated structures in the accompanying...Ch. 8.1 - Prob. 3.1SRCh. 8.1 - Prob. 3.2SRCh. 8.1 - Prob. 3.3SRCh. 8.1 - Prob. 3.4SRCh. 8.1 - Prob. 3.5SRCh. 8.1 - Prob. 3.6SRCh. 8.1 - Prob. 3.7SRCh. 8.1 - Prob. 3.8SRCh. 8.1 - Prob. 3.9SRCh. 8.1 - Prob. 3.10SRCh. 8.2 - Describe the organization and functions of the...Ch. 8.2 - Describe the innervation patterns of the...Ch. 8.2 - Describe the effects of sympathetic activation and...Ch. 8.2 - Prob. 1.1RCh. 8.2 - Prob. 1.2RCh. 8.2 - A. Starting in the spinal cord, trace the path of...Ch. 8.2 - Prob. 2.1RCh. 8.2 - Prob. 2.2RCh. 8.2 - Prob. 2.3RCh. 8.2 - Prob. 3.1RCh. 8.2 - Why is the parasympathetic division called the...Ch. 8.2 - Prob. 3.3RCh. 8.2 - Prob. 1.1SRCh. 8.2 - Prob. 1.2SRCh. 8.2 - Prob. 1.3SRCh. 8.2 - Prob. 1.4SRCh. 8.2 - Prob. 1.5SRCh. 8.2 - Prob. 1.6SRCh. 8.2 - Prob. 1.7SRCh. 8.2 - Prob. 1.8SRCh. 8.2 - Prob. 1.9SRCh. 8.2 - Prob. 2.1SRCh. 8.2 - Prob. 2.2SRCh. 8.2 - Prob. 2.3SRCh. 8.2 - Prob. 2.4SRCh. 8.2 - Prob. 2.5SRCh. 8.2 - Prob. 2.6SRCh. 8.2 - Prob. 2.7SRCh. 8.2 - Prob. 2.8SRCh. 8.2 - Prob. 2.9SRCh. 8.2 - Prob. 2.10SRCh. 8.2 - Prob. 2.11SRCh. 8.2 - Prob. 2.12SRCh. 8.2 - Prob. 2.13SRCh. 8.2 - Prob. 3SRCh. 8 - Prob. 1CRQCh. 8 - Prob. 2CRQCh. 8 - Prob. 3CRQCh. 8 - Prob. 4CRQCh. 8 - Prob. 5CRQ
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- 1) Look at the ideal results. Were your predictions accurate, and how did they compare with your results? 2) You used aseptic technique during this lab. Why is it important to work in a sterile manner when working with bacteria in the lab? 3) Why are the cells incubated at 42°C?arrow_forwardOverview of Transformation Protocol -Prepare competent bacteria for transformation: Treat starter E. coli bacteria with CaCl2and Competent Cell Solution (CCS). Store on ice until transformation procedure. Competent cells are cells that are likely to take up foreign DNA and be transformed. This step increases the likelihood that the E. coli cells will take up the introduced vector and be transformed. -Transformation procedure: Obtain two microcentrifuge tubes containing your competent cells. Label one tube +DNA and one -DNA. Add CaCl2 to both tubes. Add the transformation mix containing the plasmid DNA to the tube labeled +DNA. Do not add any plasmid DNA to the -DNA tube. Incubate both tubes on ice for 10 minutes. Then, place both tubes in a 42\deg C water bath for 45 seconds. Replace the tubes in an ice bucket for 2 minutes. Add recovery broth to both tubes. Incubate both tubes in a 37 C water bath for 5 minutes. Questions: 1) What differences would you expect to see between the…arrow_forwardOverview of Transformation Protocol -Prepare competent bacteria for transformation: Treat starter E. coli bacteria with CaCl2and Competent Cell Solution (CCS). Store on ice until transformation procedure. Competent cells are cells that are likely to take up foreign DNA and be transformed. This step increases the likelihood that the E. coli cells will take up the introduced vector and be transformed. -Transformation procedure: Obtain two microcentrifuge tubes containing your competent cells. Label one tube +DNA and one -DNA. Add CaCl2 to both tubes. Add the transformation mix containing the plasmid DNA to the tube labeled +DNA. Do not add any plasmid DNA to the -DNA tube. Incubate both tubes on ice for 10 minutes. Then, place both tubes in a 42\deg C water bath for 45 seconds. Replace the tubes in an ice bucket for 2 minutes. Add recovery broth to both tubes. Incubate both tubes in a 37 C water bath for 5 minutes. Questions: 1)What is the selectable marker in this experiment? How…arrow_forward
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