Biology

image5.jpg INCLUDEPICTURE “../images/lab007banner02.jpg” \* MERGEFORMAT image6.jpg
   

Experiment 2: The Neuromuscular Junction

image5.jpgEach skeletal muscle is connected to the nervous system be motor end units. When the neurotransmitter acetylcholine is release at this site, the muscle fiber depolarizes. Calcium ions are released from stores in the sarcoplasmic reticulum. The presence of Ca2+ triggers the ratcheting of actin and myosin filaments and the contraction of the myofiber as all of the myofibrils contract simultaneously.

Materials

Neuromuscular Junction Digital Slide Images Neuromuscular Junction (Longitudinal Section) Digital Slide Images

   

Procedure

1. Examine the digital slide images of the neuromuscular junction.

image1.png
Neuromuscular junction 100X.
image2.png
Neuromuscular Junction (Longitudinal Section) 1000X.

Post-Lab Questions

1. Identify the axon, terminal branches, and muscle fibers in the slide image below. If possible, trace the fiber to its terminus. image3.jpg

2. Are there few or many nuclei at the end plate?

3. What is a motor unit?

4. How is a greater force generated (in terms or motor unit recruitment)?

5. What types of sensors are present within the muscle to identify how much force is generated?

Experiment 3: Muscle Fatigue

Muscle contractions are essential for muscles to function properly. The inability of a muscle to maintain tension is muscle fatigue. Failure to contract may occur because of the accumulation of lactic acid, a lack of ATP, or decreased blood flow. In this exercise, you will investigate the correlation between repeated movements and muscle fatigue.

image6.jpg

Materials

Rubber Band

Stopwatch

Note: If you suffer from a medical condition that does not permit you to perform this activity, please ask a partner to volunteer for you.

Procedure

1. Hypothesize how many times you can stretch a rubber band between your thumb and pinky finger in 20 seconds. Record your predictions in the table below.

2. Using your dominant hand, count the number of times you can completely stretch a rubber band between the thumb and pinky finger in 20 seconds. Be sure to stretch the rubber band as far as possible each time and do not take a break in between trials.

3. Record your count for each trial in Table 1.

Table 1: Experimental Counts
  Trial 1 Trial 2 Trial 3 Trial 4 Trial 5
Predicted Value          
Actual Value          

Post-Lab Questions

1. How did the predicted results compare to the actual results?

2. Did you notice any changes in the number of repetitions you could perform, or how your hand felt after each of the trials?

3. Explain the actions that were occurring at the cellular level to produce this movement. Include sources of energy and any possible effect of muscle fatigue.

4. Hypothesize what would happen if blood flow was restricted to the hand when this experiment is performed.

Experiment 4: Gross Anatomy of the Muscular System

image7.jpgMuscle actions are often described as a departure of the from the anatomical position of the body. In performing the next exercise, you will understand how muscles act to affect motion.

Materials

*Participant (can be yourself) *Heavy Object (approximately 5 pounds)

*You must provide

Procedure

1. Begin by examining muscles found in the upper limbs. First, extend your forearm so you have a clear view of your hand. What muscle is required to perform this extension? Extend your fingers out so they are straight and splayed apart. Then, retract your fingers into a tight fist. Repeat this motion several times, observing the wrist and hand muscles as the flex and relax. What muscles are used to complete this action? Record your observations in Table 2.

Note: It is helpful to palpate the area being flexed to better identify which muscles are being used.

2. Moving up the limb, extend your forearm out until it is parallel to the ground. Have a partner press down on your forearm. Flex your forearm to provide resistance as your partner pushes down. Observe the forearm and identify which muscles are being used. Record your observations in Table 2.

3. The partner should stop pushing down on your forearm, but keep it extended. Curl the forearm upward, creating a bend at the elbow. Observe which muscles are being used to complete this action, and record your observations in Table 2.

4. Find a heavy object, and pick it up. Keeping your arm straight, raise the object out to the side until it is parallel to the ground. What muscles does this require? Continue holding the object, and extend your arm back behind you. What muscles does this activate? Record your observations in Table 2.

Note: Be sure the heavy object is not too heavy before you lift it. This item should be approximately 5 – 10 pounds. This object should never be raised above your head!

5. Move down to the lower limbs, and determine what motions are needed to view the lower limb muscles in action. For example, you may want to walk, jump, sit, point your toes, etc. Engage at leave seven different muscles and indicate what motion was used to engage each muscle in Table 2.

Table 2: Gross Anatomy Data
Movement Muscle(s) Activated Action(s) of Muscle(s)
1. Forearm Extended (Step 1)    
2. Fingers Extended and  Splayed (Step 1)    
3. Fingers Retracted (Step 1)    
4.  Forearm Pressed Down Upon (Step 2)    
5. Elbow Bent (Step 3)    
6. Arm Raised to Side with Heavy Object (Step 4)    
7. Arm Extended Back with Heavy Object (Step 4)    
8. (lower limbs; student selects action…)    
9. (lower limbs; student selects action…)    
10. (lower limbs; student selects action…)    
11. (lower limbs; student selects action…)    
12. (lower limbs; student selects action…)    
13. (lower limbs; student selects action…)    
14. (lower limbs; student selects action…)    
 

Post-Lab Questions

1. Label the human muscle diagram.

image4.jpg

2. Which muscle(s) were used to extend your arm backwards?

3. Which muscle(s) were used to extend and splay your fingers outward?

Experiment 5: ATP and Muscle Fatigue

Muscles require energy to contract. Energy is released when biomolecules such as sugars and fats are broken down, and is stored in the form of ATP. ATP enables muscle contraction, but can only be stored in relatively small amounts. For this reason, the body must continually metabolize new ATP molecules.

image8.jpgMuscle fatigue occurs if the local ATP reservoir for a muscle becomes depleted. This is a common result of strenuous exercise in which ATP is consumed at a faster rate than it is produced. At this point, muscles may fail to contract and the intensity of an exercise must decrease. In this experiment, you will test how long it takes your muscles to fatigue.

Materials Stopwatch *Participant *Sturdy Wall to Stand Against *You must provide

Procedure

1. To begin, find a wall that is strong enough for you to push against. A temporary wall (such as a partition panel) is not suitable.

2. Find the stopwatch and adjust the settings so it is ready to operate.

3. Stand with your back pressed up against the wall, and lower yourself into a “wall-sit”. To do this:

a. Align the backs of your heels, hips, and shoulders with the wall.

b. Keeping your back pressed against the wall, take a few small steps forward (your upper half will lower as you walk your feet out).

c. Lower yourself into a sitting position, keeping your back flat against the wall, until your knees form a 90 degree angle.

d. Steady this position by focusing the majority of your weight in your heels. Do not allow your lower back to pull away from the wall.

4. Start the stopwatch and time how long you are able to hold the wall-sit position. The amount of time will vary, but will likely fall within approximately 30 – 120 seconds. When you are tired, check the time on the stopwatch, and move out of the position by slowly lowering your body down to the floor or standing up.

5. Record how long you were able to hold the wall-sit in Table 3.

6. Allow your muscles to rest for approximately two minutes, reset the stopwatch, and repeat Steps 3 – 5.

7. Again, allow your muscles to rest for approximately two minutes, reset the stopwatch, and repeat Steps 3 – 5. You should have three trials of data.

Table 3: Muscle Fatigue Data
Trial Time (seconds)
Trial 1  
Trial 2  
Trial 3  

 

Post-Lab Questions

1. What happened to the time intervals between Trial 1 and Trial 3? What caused this change?

2. Identify three muscles which were engaged during the wall-sit.

3. Explain the biochemical reasoning behind muscle fatigue.

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Scin Work Wk7

SCIN 130 Lab 7: CSI Wildlife, Case 1

General Instructions

Be sure to read the general instructions from the Lessons portion of the class prior to completing this packet.

Remember, you are to upload this packet with your quiz for the week!

Background

The scenarios investigated are based on the recently published literature: Wasser, S. K., Brown, L., Mailand, C., Mondol, S., Clark, W., Laurie, C., & Weir, B. S. (2015). Genetic assignment of large seizures of elephant ivory reveals Africa’s major poaching hotspots. Science, 349(6243), 84–87. The underlying data are available on the Dryad Digital Repository: http://dx.doi.org/10.5061/dryad.435p4.

Remember, DNA is made up of nucleotides and an allele is an alternative form of a gene which may be from mutation, but is found on the same place in a chromosome in individuals and functions similarly. If you are unfamiliar with these terms, make sure to review them in your book prior to completing the lab.

Specific Lab Instructions

Name:     

Date:

Go to: CSI Wildlife on HHMI Biointeractive

Part 1: The Introduction

1. Read the instructions on the home page. Then, watch the opening video from the CSI Wildlife Introduction.

2. What is a keystone species?

SCIN 130 Lab 7: CSI Wildlife, Case 1

V1 04.2018 Felicetti

Page 1 of 9

3. Dr. Wasser states that approximately 50,000 African elephants are killed each year. According to the video, it is estimated that there are around 470,000 African elephants. If these numbers are correct, approximately what percentage of African elephants are killed each year? (Show your work.

4. In one or two sentences, summarize Dr. Wasser’s research and how it is being used to conserve elephants.

Part 2: Case One

1. Watch the crime scene video on the first slide of Case One. Explain the goal of the case.

2. Look at the map provided; in what type of location are the majority of African elephants located?

3. Proceed to the How DNA Profiling Works section.

a.

b. What does “STR” stand for and how are they important for identification?

c. Look at the gel on the screen. What do the bands on the agarose gel represent?

d. What is the purpose of the DNA ladder on the agarose gel?

e. DNA profiling is also called DNA fingerprinting. A common misconception about DNA fingerprinting is that the analysis has to do with actual fingerprints. Explain one similarity and one difference between a human being’s pattern of bands on an electrophoresis gel and a human fingerprint.

4

5. Click on Technique.

a. List three sources to obtain elephant DNA for analysis.

b. Watch the animation on the polymerase chain reaction under Technique. What is the purpose of heating the DNA strand? What is the purpose of cooling the DNA strand?

c. What is the relationship between the size of a DNA fragment and the distance it migrates in the gel?

d. Why does DNA migrate to the positive electrode?

e. Run the gel in the Technique section by pressing the Start button. Which elephant (left or right) has both the largest and smallest fragments?       Approximately what size is the largest fragment (bp)?       Smallest?      .

6. Proceed to the Application section and look at the gel.

a. For Marker C, are the two elephants in the gel on the left homozygous or heterozygous? How do you know?

7. Read the Review section, and make sure you can answer the questions.

8.

9. Go to Finding a Match

a. Click on the “+” next to each marker. Compare the bands in the agarose gel from the unidentified elephant and the known elephants. Which elephant (there are two pages of them) matches the unidentified elephant?

10. Watch the video on the “Case Solved” slide.

a.

b. Name two properties of a good marker and explain why good markers are important.

Adapted from: Click and Learn “CSI Wildlife” (2016). CSI Wildlife Explorer Worksheet. HHMI Biointeractive Teaching Materials.

 
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UMUC Biology 102/103 Lab 2: The Chemistry Of Life ANSWER KEY

This is the correct material for UMUC Biology 102/103 Lab 2: The Chemistry of Life. However, this is an Answer Key, which means, you should put it in your own words. Here are the questions that will be answered. Attached is the lab that is fully completed when purchased. Enjoy!

Pre-Lab Questions

1.    Nitrogen fixation is a natural process by which inert or unreactive forms of nitrogen are transformed into usable nitrogen. Why is this process important to life?

2.    Given what you have learned about the hydrogen bonding shared between nucleic acids in DNA, which pair is more stable under increasing heat: adenine and thymine, or cytosine and guanine? Explain why.

3.    Which of the following is not an organic molecule; Methane (CH4), Fructose(C6H12O6), Rosane (C20H36), or Ammonia (NH3)? How do you know?

Experiment 1: Testing for Proteins

Data Tables and Post-Lab Assessment

Table 1: A Priori Predictions

Sample Initial Color Final Color Is Protein Present?
1. Albumin Solution      
2. Gelatin Solution      
3. Glucose      
4. Water      
5. Unknown      

 

Sample Initial Color Final Color Is Protein Present?
1. Albumin Solution      
2. Gelatin Solution      
3. Glucose      
4. Water      
5. Unknown      

Table 2: Testing for Proteins Results

Post-Lab Questions

1.    Write a statement to explain the molecular composition of the unknown solution based on the results obtained during testing with each reagent.

2.    How did your a priori predictions from Table 1 compare to your actual results in Table 2? If there were any inconsistencies, explain why this occurred.

3.    Identify the positive and negative controls used in this experiment. Explain how each of these controls are used, and why they are necessary to validate the experimental results.

4.    Identify two regions which proteins are vital components in the human body. Why are they important to these regions?

5.    Diet and nutrition are closely linked to the study of biomolecules. Describe one method by which you could monitor your food intake to ensure the cells in your body have the materials necessary to function.

Experiment 2: Testing for Reducing Sugars

Data Tables and Post-Lab Assessment

Table 3: Testing for Reducing Sugars Results

Sample Initial Color Final Color Reducing Sugar Present
1 – Potato      
2 – Onion      
3 – Glucose Solution      
4 – Water      
5 – Unknown      

Post-Lab Questions

1.    What can you conclude about the molecular make-up of potatoes and onions based on the test you performed? Why might these foods contain these substance(s)?

 

2.    What results would you expect if you tested ribose, a monosaccharide, with Benedict’s solution? Biuret solution?

Experiment 3: What Household Substances are Acidic or Basic?

Data Tables and Post-Lab Assessment

Table 4: pH Values of Common Household Substances

Substance pH Prediction pH Test Strip Color
     
     
     
     
     

Post-Lab Questions

1.    What is the purpose of determining the pH of the acetic acid and the sodium bicarbonate solution before testing the other household substances?

2.    Compare and contrast acids and bases in terms of their H+ ion and OH ion concentrations.

3.    Name two acids and two bases you often use.

 
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The Hardy-Weinberg Equation

The Hardy-Weinberg Equation 1
The Hardy-Weinberg Equation
How can we make predictions about the characteristics of a population?
Why?
Punnett squares provide an easy way to predict the possible genotypes for an offspring, but it is not practical
to perform a Punnett square analysis on all possible combinations of all members of a population to
predict what the population might look like in the future. For that we must turn to statistics. The HardyWeinberg
equation is a tool biologists use to make predictions about a population and to show whether or
not evolution is occurring in that population.
Model 1 – Controlled (Selective) Mating
Bb
Bb
Bb
bb
bb
bb
Bb
Bb
Bb
bb
bb
bb
Males Females
Bb
Bb
Bb
bb
bb
bb
Males Females
Bb
Bb
Bb
bb
bb
bb
1. How many mating pairs are illustrated in Model 1?
2. Describe the parents in each mating pair in Model 1. Use terms such as homozygous, heterozygous,
dominant, and recessive.
3. Use two Punnett squares to determine the possible genotypes for offspring from the pairs.
2 POGIL™ Activities for AP* Biology
4. If each mating pair has one offspring, predict how many of the first generation offspring will
have the following genotypes.
BB Bb bb
5. Imagine the 24 beetles in Model 1 as a population in an aquarium tank.
a. How likely is the pairing scenario in Model 1 to take place during the natural course of things
within that tank?
b. Why is Model 1 labeled “Selective Mating”?
6. List two other pairings that might occur in the population in Model 1 if the beetles were allowed
to mate naturally.
7. If the population of beetles in Model 1 mated naturally would your prediction for the offspring
in Question 4 still be valid? Explain.
8. Discuss in your group the limitations of Punnett square predictions when it comes to large populations.
Summarize the key points of your discussion here.
The Hardy-Weinberg Equation 3
Model 2 – Population Genetics
Bb bb
Bb Bb
Bb Bb
Bb bb
bb bb
bb bb
Bb bb
Bb Bb
Bb Bb
Bb bb
bb bb
bb bb
Males Females
9. Compare the organisms in the population in Model 1 with the organisms in the population in
Model 2.
10. Individually match up twelve mating pairs from the population in Model 2 that might occur in a
natural, random mating situation.
11. Compare your set of mating pairs with other members of your group. Did your mating scheme
match anyone else’s in the group?
4 POGIL™ Activities for AP* Biology
Read This!
When it comes to mating in natural populations with hundreds or even millions of individuals, it is diffi
cult, maybe even impossible, to think of all the mating scenarios. After several generations of leaving
things up to nature, the alleles that are present in the population will become more and more randomized.
Statistics can help biologists predict the outcome of the population when this randomization has occurred.
If the population is particularly nonrandom to start, this randomization may take several generations.
12. How many total alleles are in the population in Model 2?
13. What is the probability of an offspring from the Model 2 population getting a dominant allele?
14. What is the probability of an offspring from the Model 2 population getting a recessive allele?
15. If p is used to represent the frequency of the dominant allele and q is used to represent the frequency
of the recessive allele, then what will p + q equal?
16. Use your knowledge of statistics to calculate the probability of an offspring from the Model 2
population having each of these genotypes. Support your answers with mathematical equations.
(Don’t forget there are two ways to get a heterozygous offspring—Bb or bB.)
BB Bb bb
17. Check your answers in Question 16 by adding the three values together. Your sum should be
equal to one. Explain why the sum of the three answers in Question 16 should be equal to one.
18. Using p and q as variables, write formulas for calculating the probability of an offspring from a
population having each of the following genotypes.
BB Bb bb
19. Complete the equation:
p2
+ 2pq + q2
=
The Hardy-Weinberg Equation 5
Read This!
The equations you have just developed, p + q = 1 and p2
+ 2pq +q2
= 1, were fi rst developed by G. H.
Hardy and Wilhelm Weinberg. They represent the distribution of alleles in a population when
• The population is large.
• Mating is random.
• All genotypes are equally likely to reproduce (there is no natural selection).
• No organisms enter or leave the population (there is no immigration or emigration).
• No mutations occur.
In other words, the group of alleles available in the population must be very stable from generation
to generation. If the distribution of genotypes in a population matches that predicted by the HardyWeinberg
equation, then the population is said to be in Hardy-Weinberg equilibrium. If the distribution
of genotypes in a population does not match that predicted by the Hardy-Weinberg equation, then the
population is said to be evolving.
20. Consider the requirements for a population to be in Hardy-Weinberg equilibrium. In the natural
world, are populations likely to be in Hardy-Weinberg equilibrium? Justify your reasoning.
21. Sickle-cell anemia is a genetic disease. The Sickle-cell allele is recessive, but individuals with the
homozygous recessive genotype (ss) often die prematurely due to the disease. This affects approximately
9% of the population in Africa. Use the Hardy-Weinberg equations to calculate the
following:
a. The frequency of the recessive allele in the population (q).
b. The frequency of the dominant allele in the population (p).
c. The frequency of homozygous dominant individuals in the African population.
d. The frequency of heterozygous individuals in the African population.
e. Based on this analysis, is the African population in Hardy-Weinberg equilibrium? Justify your
answer.
6 POGIL™ Activities for AP* Biology
22. Individuals with the heterozygous genotype (Ss) for Sickle-cell exhibit resistance to Malaria, a
serious disease spread by mosquitoes in Africa and other tropical regions.
a. Discuss with your group how this might affect the frequency of the recessive allele in the
African population. Summarize your group’s conclusions here.
b. How might this trait affect the values calculated in Question 21 and the population’s
tendency toward Hardy-Weinberg equilibrium?
23. Consider the beetle population in Model 2. Imagine a change occurred in the beetle’s ecosystem
that made it easier for predators to spot the white beetles and six of the white beetles were lost.
Predict the genotype frequency in the population after this event.
24. Compare your answers to Question 22 with those of Question 16. How do your answers support
the conclusion that the population is not in Hardy-Weinberg equilibrium?
The Hardy-Weinberg Equation 7
Extension Questions
25. The ability to taste PTC is due to a single dominant allele “T.” You sampled 215 individuals and
determined that 150 could detect the bitter taste of PTC and 65 could not. Calculate the following
frequencies.
a. The frequency of the recessive allele.
b. The frequency of the dominant allele.
c. The frequency of the heterozygous individuals.
26. Sixty flowering plants are planted in a flowerbed. Forty of the plants are red-flowering homozygous
dominant. Twenty of the plants are white-flowering homozygous recessive. The plants
naturally pollinate and reseed themselves for several years. In a subsequent year, 178 red-flowered
plants, 190 pink-flowered plants, and 52 white-flowered plants are found in the flowerbed. Use a
chi-square analysis to determine if the population is in Hardy-Weinberg equilibrium.

 
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Biology Lab Work 4 Assistance

 

UMUC Biology 102/103

Lab 4: Enzymes

INSTRUCTIONS:

·         On your own and without assistance, complete this Lab 4 Answer Sheet electronically and submit it via the Assignments Folder by the date listed in the Course Schedule (under Syllabus).

·         To conduct your laboratory exercises, use the Laboratory Manual located under Course Content. Read the introduction and the directions for each exercise/experiment carefully before completing the exercises/experiments and answering the questions.

         Save your Lab 4 Answer Sheet in the following format:  LastName_Lab4 (e.g., Smith_Lab4).

·         You should submit your document as a Word (.doc or .docx) or Rich Text Format (.rtf) file for best compatibility.

Pre-Lab Questions

  1. How could you test to see if an enzyme was completely saturated during an experiment?
  2. List three conditions that would alter the activity of an enzyme. Be specific with your explanation.
  3. Take a look around your house and identify household products that work by means of an enzyme. Name the products, and indicate how you know they work with an enzyme.

Experiment 1: Enzymes in Food

Data Tables and Post-Lab Assessment

Table 1: Substance vs. Starch Presence

Table 1: Substance vs. Starch Presence
Substance Resulting Color Presence of Starch?
Positive Control: Ginger Root    
Negative Control: Student Must Select    
Food Product:    
Food Product:    
Saliva:    

Post-Lab Questions

 

  1. What were your controls for this experiment? What did they demonstrate? Why was saliva included in this experiment?
  2. What is the function of amylase? What does amylase do to starch?
  3. Which of the foods that you tested contained amylase? Which did not? What experimental evidence supports your claim?
  4. Saliva does not contain amylase until babies are two months old. How could this affect an infant’s digestive requirements?
  5. There is another digestive enzyme (other than salivary amylase) that is secreted by the salivary glands. Research to determine what this enzyme is called. What substrate does it act on? Where in the body does it become activated, and why?
  6. Digestive enzymes in the gut include proteases, which digest proteins. Why don’t these enzymes digest the stomach and small intestine, which are partially composed of protein?

Experiment 2: Effect of Temperature on Enzyme Activity

Data Tables and Post-Lab Assessment

Table 2: Balloon Circumference vs. Temperature

Table 2: Balloon Circumference vs. Temperature
Tube Temperature (°C) Uninflated Balloon Circumference (cm) Final Balloon Circumference (cm) Difference in Balloon Circumference (cm)
1 – (Cold)        
2 – (RT)      
3 – (Hot)      

 

 

Post-Lab Questions

  1. What reaction is being catalyzed in this experiment?
  2. What is the enzyme in this experiment? What is the substrate?
  3. What is the independent variable in this experiment? What is the dependent variable?
  4. How does the temperature affect enzyme function? Use evidence from your data to support your answer.
  5. Draw a graph of balloon diameter vs. temperature. What is the correlation?
  6. Is there a negative control in this experiment? If yes, identify the control. If no, suggest how you could revise the experiment to include a negative control.
  7. In general, how would an increase in substrate alter enzyme activity? Draw a graph to illustrate this relationship.
  8. Design an experiment to determine the optimal temperature for enzyme function, complete with controls. Where would you find the enzymes for this experiment? What substrate would you use?
 
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UMUC Biology 102 / 103 Lab 3: Cell Structure And Function ANSWER KEY

This contains 100% correct material for UMUC Biology 103 LAB03. However, this is an Answer Key, which means, you should put it in your own words. Here is a sample for the Pre lab questions answered:

Pre-Lab Questions

1. Identify the major similarities and differences between prokaryotic and eukaryotic cells. (2 pts)

Prokaryotes tend to be less complex than eukaryotic cells, with fewer organelles and (generally) fewer requirements for survival. Eukaryotes have a nucleus, while prokaryotes do not. Both eukaryotes and prokaryotes have DNA, a cell membrane, and cytoplasm.

2. Where is the DNA housed in a prokaryotic cell? Where is it housed in a eukaryotic cell? (2 pts)

DNA is housed in the nucleus in eukaryotic cells. Prokaryotic cells do not have a nucleus, and thus DNA exists freely in the cytoplasm.

3. Identify three structures which provide support and protection in a eukaryotic cell. (2 pts)

The cell membrane, the cytoplasm, and the cytoskeleton (microtubules, microfilaments, etc.).

The rest of the questions are answered as well:

Onion Root Tip 100X g (Small)

Experiment 1: Cell Structure and Function

Post-Lab Questions

1.    Label each of the arrows in the following slide image:

2.    What is the difference between the rough and smooth endoplasmic reticulum?

3.    Would an animal cell be able to survive without a mitochondria? Why or why not?

4.    What could you determine about a specimen if you observed a slide image showing the specimen with a cell wall, but no nucleus or mitochondria?

5.    Hypothesize why parts of a plant, such as the leaves, are green, but other parts, such as the roots, are not. Use scientific reasoning to support your hypothesis.

Experiment 2: Osmosis – Direction and Concentration Gradients

Data Tables and Post-Lab Assessment

Table 3: Sucrose Concentration vs. Tubing Permeability

Band Color Sucrose % Initial Volume (mL) Final Volume (mL) Net Displacement (mL)
Yellow        
Red        
Blue        
Green        

Hypothesis:

Post-Lab Questions

1.    For each of the tubing pieces, identify whether the solution inside was hypotonic, hypertonic, or isotonic in comparison to the beaker solution in which it was placed.

2.    Which tubing increased the most in volume? Explain why this happened.

3.    What do the results of this experiment this tell you about the relative tonicity between the contents of the tubing and the solution in the beaker?

4.    What would happen if the tubing with the yellow band was placed in a beaker of distilled water?

5.    How are excess salts that accumulate in cells transferred to the blood stream so they can be removed from the body? Be sure to explain how this process works in terms of tonicity.

6.    If you wanted water to flow out of a tubing piece filled with a 50% solution, what would the minimum concentration of the beaker solution need to be? Explain your answer using scientific evidence.

7.    How is this experiment similar to the way a cell membrane works in the body? How is it different? Be specific with your response.

 
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Microscopy For Microbiology – Use And Function Hands-On Labs, Inc. Version 42-0249-00-02

Microscopy for Microbiology – Use and Function

Hands-On Labs, Inc. Version 42-0249-00-02

Lab Report Assistant

This document is not meant to be a substitute for a formal laboratory report. The Lab Report Assistant is simply a summary of the experiment’s questions, diagrams if needed, and data tables that should be addressed in a formal lab report. The intent is to facilitate students’ writing of lab reports by providing this information in an editable file which can be sent to an instructor.

Exercise 1: Getting to Know your Compound Microscope

Data Table 1. Microscope Components.

Letter Component Name Component Function
A    
B    
C    
D    
E    
F    
G    
H    
I    
J    
K    
L    
M    

 

Data Table 2. Total Magnification.

Lens Ocular Magnification Objective Magnification Total Magnification
Scanning      
Low Power      
High Power      
Oil Immersion      

Data Table 3. Field of View.

Lens Total Magnification Field of View (mm) Field of View (µM)
Scanning      
Low Power      
High Power      
Oil Immersion      

 

Data Table 4. Letter e Viewing Results.

Lens Photograph Observations
Scanning    
Low    
High    
Oil Immersion    

 

Questions

A. Describe the details in the slides “Letter e” that become visible as the power changed from scanning power, to low power, to high power.

B. Why is it important to calculate the diameter of the field when first using the microscope?

Exercise 2: Viewing Prepared Microbe Slides

Data Table 5. Prepared Slide Viewing Results.

Slide Photograph Total Magnification
Amoeba  

 

 

 
Penicillium  

 

 
Yeast  

 

 

 
Spirillium  

 

 

 
Bacillus  

 

 

 
Coccus  

 

 

 

 

Questions

A. Using the field of view calculated in Exercise 1 for the high power lens, approximately how far across are each of the cells in the Bacteria Coccus Form slide in Data Table 5? Show your calculations.

B. Detail techniques you found helpful for focusing on the various slides in this exercise.

Exercise 3: Preparing Wet-Mount Slides

Data Table 6. Wet-Mount Viewing Results.

Slide Photograph Total Magnification
Cheek Cell Smear  

 

 

 
Dental Tatar Smear  

 

 

 

 

Questions

A. Describe the similarities and differences between the cheek cell wet mount and dental plaque wet mount.

B. How did the process of preparing wet-mount slides become easier as you prepared the second wet-mount slide of this exercise?

 
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BIO GENETICS LAB 2 QUESTIONS HELP

NEED HELP WITH BLANK BOX QUESTION

(question 1 and 4 in conclusion part. )

* It would be nice if you can check my answeres too.

NOTES:

Tube Sample Lane

1 1 kb DNA ladder 1

2 Mother’s DNA 2

3 Child’s DNA 3

4 A.F. #1 DNA 4

5 A.F. #2 DNA 5

Record the distance each ladder band moved from the well in mm along with the size of the DNA fragments in that band in bp units, based on the bp given in step 19 , in your Lab Notes.

Lane 1:

1,000 bp 34 mm

900 bp 36 mm

800 bp 38 mm

700 bp 40 mm

600 bp 43 mm

500 bp 47 mm

400 bp 51 mm

300 bp 56 mm

250 bp 60 mm

200 bp 64 mm

150 bp 69 mm

100 bp 77 mm

50 bp 90 mm

Lane 2:

37 mm 850bp

59 mm 265bp

Lane 3:

37 mm 850bp

44 mm 575bp

Lane 4:

41 mm 670bp

43 mm 600bp

Lane 5:

44 mm 575bp

55 mm 320bp

Experiment: Agarose Gel Electrophoresis of DNA Fragments

Lab Results

  1. List the distances traveled in mm for the bands in the DNA ladder in the table below.
    Remember, smaller fragments travel farther than longer ones, so the top-most band will be the 1,000 bp sized DNA fragments whereas the bottom-most band will be the 50 bp sized DNA fragments. 

    DNA Ladder
    Band Distance (mm)
    50 bp  90 mm
    100 bp  77 mm
    150 bp  69 mm
    200 bp  64 mm
    250 bp  60 mm
    300 bp  56 mm
    400 bp  51 mm
    500 bp  47 mm
    600 bp 43 mm
    700 bp 40 mm
    800 bp 38 mm
    900 bp 36 mm
    1,000 bp 34 mm
  2. Whose sample had the approximately 570 bp and 320 bp sized DNA fragments?
     A.F. #2
  3. What were the sizes of the DNA fragments for alleged father #1?
    41 mm 670bp

    43 mm 600bp

Data Analysis

  1. Which size DNA fragment did the child inherit from her mother?
     37 mm 850bp
  2. Which alleged father, if any, can be definitively ruled out as the child’s biological father?
     A.F. #2

Conclusions

  1. How are new molecules of DNA synthesized in living cells?
  2. What is the function of DNA?
     

    DNA has genetic information that controls our cells. So, DNA is like a blueprint that shows how to construct components of cells like proteins and ribonucleic acid (RNA). This information is carried down to newer generations through inheritance.

  3. If each individual has such a small amount of DNA in their cells, how do the bands on the gel contain enough DNA to be visible?
      In order to make DNA visible. The Gel has to be soaked in a dye (ethidium bromide) to bind with the DNA and rinsed off after. Ethidium bromide helps to make DNA visible by glowing brightly in UV rays.
  4. Humans only have a few eye colors and only four ABO-based blood types. How can DNA tests definitively identify individuals when many people have brown eyes or type A blood?
  5. Suppose a suspicious hair was found in a victim’s home. A gel is set up with the DNA fragments of two suspected criminals in lanes 4 and 5, the DNA fragments of the suspicious hair in lane 3, and the victim’s DNA fragments, as a negative control, are in lane 2. A DNA ladder is in lane 1. The resulting gel is below. Which suspect, if any, committed the crime? Explain your answer.
 
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Biology Lab Assignments

Lab 2 Cell Structure and Function BIO101L

Student Name: Click here to enter text.

Access Code (located on the lid of your lab kit): Click here to enter text.

Pre-Lab Questions

1. Identify three major similarities and differences between prokaryotic and eukaryotic cells.

Click here to enter text.

2. Where is the DNA housed in a prokaryotic cell? Where is it housed in a eukaryotic cell?

3. Identify three structures which provide support and protection in a eukaryotic cell.

Experiment 1: Identifying Cell Structures

Post-Lab Questions

1. Label each of the arrows in the following slide image:

Structure Identity
A Click here to enter text.
B Click here to enter text.
C Click here to enter text.
D Click here to enter text.

 

2. What is the difference between the rough and smooth endoplasmic reticulum?

3. Would an animal cell be able to survive without mitochondria? Why or why not?

4. What could you determine about a specimen if you observed a slide image showing the specimen with a cell wall, but no nucleus or mitochondria?

5. Hypothesize why parts of a plant, such as the leaves, are green, but other parts, such as the roots, are not. Use scientific reasoning to support your hypothesis.

Experiment 2: Create a Cell

Post-Lab Questions

1. What cell structures did you place in the plant cell that you did not place in the animal cell?

2. Is there any difference in the structure of the two cells?

3. What structures do cells have for support in organisms that lack cell walls?

4. How are organelles in a cell like organs in a human body?

5. How does the structure of a cell suggest its function? List three examples.

6. In the table below, list the items you used to represent the various organelles in your ANIMAL cell. Provide a brief rationale explaining why you selected each item.

Item Organelle Rationale
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.

 

7. Insert picture of your ANIMAL cell with your name and access code handwritten in the background.

8. In the table below, list the items you used to represent the various organelles in your PLANT cell. Provide a brief rationale explaining why you selected each item.

Item Organelle Rationale
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.
Click here to enter text. Click here to enter text. Click here to enter text.

 

9. Insert picture of your PLANT cell with your name and access code handwritten in the background.

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Anthropology Exam

Beginning Thoughts on Anthropology, Culture & Cultural Diversity

1.)What ideas or images that come to mind if someone says “Anthropology” or “anthropologist”? What has shaped your ideas about what Anthropology is or what Anthropologists do?

2.)What IS Anthropology? And what are the four sub-fields of Anthropology?

3.)Some contemporary archaeologists focus on studying modern human waste….including e-waste. If someone were to study YOUR waste (trash) …and e-waste what would they learn about you? Your diet? Your lifestyle?

4.) What are some cultural adaptations human beings have to better allow them to survive in their environment? Are there negative effects of these adaptations? If so, do the benefits outweigh those negative effects?

5.)American anthropologist Ralph Linton once said “The last thing a fish would ever notice would be water.” (Ralph Linton, 1936) How is this relevant and applicable to a discussion on “culture”?

6.) Polish anthropologist, Bronislaw Malinowski who is credited with inventing the anthropological method of intensive fieldwork, wrote in his journal about his fieldwork in the Trobriand Islands.In his diary he wrote” Imagine yourself suddenly set down surrounded by all your gear, alone on a tropical beach close to a native village, while the launch or dinghy which has brought you sails away out of sight.” What is Malinowski describing? Have you ever had an analogous experience in Philadelphia (or elsewhere)?

7.)Clifford Geertz, one of the most influential American anthropologists in the last 40 years, said “The locus of study is not the object of study. Anthropologists don’t study villages (tribes, neighborhoods…) they study in villages.” What do you think he meant? (And what happens if you substitute college for village?)

8.) If I were to ask you to provide a “socio-cultural analysis” of this classroom…where would you begin? Can you identify 10 ways that you might consider “diversity” within this classroom? (on campus, in the city, in the U.S. or in the world?)

9.) How do you think about diversity? i.e.as a problem? A challenge? An asset? Explain

10.) What do you think is bigger…a nation-state or a culture? Briefly explain.

 
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