How many of each phenotype are there? You may find it helpful to answer this question by selecting the “Analyze” tab, and checking the box labeled “Ignore sex of flies,” as shown in the image on the previous page.

Genetics

Your Assignment –

You will be setting up several fly crosses, comparing offspring ratios, and determining the mode of inheritance of those genes. We will be using mutants in the white gene and in the miniature gene for this lab. The white gene and the miniature gene are both located on the X chromosome.  Follow the instructions below, and answer all questions.

 

Part I

Cross #1:

Select a female fly with the White Eye Color trait, and mate her to a male fly with the Miniature Wing Size trait.

Q1. What are the phenotypes of the offspring from this cross?

Q2. How many of each phenotype are there? You may find it helpful to answer this question by selecting the “Analyze” tab, and checking the box labeled “Ignore sex of flies,” as shown in the image on the previous page.

Cross #2:

Select the female offspring of cross #1, and mate her to a male fly showing both the White Eye Color trait and the Miniature Wing Size trait.

Q3. What are the phenotypes of the offspring from this cross?

Q4. How many of each phenotype are there?

Q5. Assume these genes are inherited through simple Mendelian inheritance. Set up a Punnett’s Square of cross #2. Do the Punnett’s Square results match the results you observe?  Explain why or why not.

Q6. Write the genotypes of each of the parents and offspring in crosses #1 and #2. Remember, these genes are on the X chromosome.

Q7. Are the mutant alleles in the female parent in cross #2 in cis or in trans? Draw a diagram of the arrangement of her alleles on both of her X chromosomes.

Q8. For each gene, which alleles are dominant and negative?

Q9. Consider your answer to Q8. What is the name for the specific type of cross you set up for cross #2?

Q11. Propose a non-Mendelian mode of inheritance for the white and miniature genes.

Q12. How far apart on the X chromosome are the white and miniature genes? You must show all work to receive any credit for this question.

Part II

Repeat crosses #1 and #2 using either one of the two genes listed above and the Yellow allele of the Body Color trait. Then answer questions #6 and #12 for these new crosses.

 

Write an essay explaining why we can’t transfer animal blood into human body.

Scientific language opinnion essay

Write an essay explaining why we can’t transfer animal blood into human body.

Discuss the types of Bacteriostatic antibiotics and the importance of a functioning immune system.

Types of Bacteriostatic antibiotics

This essay must focus on The specific class of antiobiotic (Bacteriostatic) and how it prevents cell replication. It must also tie in how it affects protein synthesis in the cell and the cell in general. Also discuss the types of Bacteriostatic antibiotics and the importance of a functioning immune system.

 

Write an essay on how does restricted end onuclease work.

Uclease work

Write an essay on how does restricted end on uclease work.

 

Summarize the career, summarize how neuroscience is involved in the career, discuss education and experience requirements for the career.

DISCUSSION ESSAY

Information: You will select an unconventional career in neuroscience, or highlight a conventional career that utilizes neuroscience in ways you did not realize. You do not need peer-reviewed journal articles as your sources, as this is more of an exploration exercise to see just how valuable your major is! However, citations are required for any websites, articles, etc. that you use.

Paper content: Summarize the career, summarize how neuroscience is involved in the career, discuss education and experience requirements for the career.

Can an action potential be triggered without ion flow occurring? Can an action potential occur if there is not the correct concentrations of ions on the outside and the inside of the cell?

Modeling Ion Movement

In this lab we will explore the importance of ion balance in neurotransmission. In part one you will model how ions move in and out of a neuron due to channels opening. Then in part two you will use a computer simulation to look at how ion distributions across the cell membrane (plasma membrane) make an action potential possible.

 You will make a hypothesis that talks about how ion balance is important for neuron transmission. Remember that transmission (communication from one neuron to a another) can only happen when an action potential is triggered. Here are some questions to consider when framing your hypothesis. Make a hypothesis that integrates these questions.

  1. Can an action potential be triggered without ion flow occurring?
  2. Can an action potential occur if there is not the correct concentrations of ions on the outside and the inside of the cell?

Now that you have a hypothesis we will test the hypotheses with some modeling! In part one we are using physical models to look at how channels opening allow ion flow down their concentration gradients. In part two we will use a computer model to ask how important the precise ionic concentrations are to be able to trigger action potentials.

 

Lab 3 – Part 1:

Understanding ion flow:

Grab 1 clear plastic cups, 1 paper cups, and a pin. Put an inch of water in the clear plastic cup, fill the paper cup with water. Put the paper cup inside the clear plastic cup. Add 5-10 drops of food coloring the water inside the paper cup. Now, lift the paper cup up, take the pin and puncture the side of the paper cup. Now put it back into the clear plastic cup. Describe what happens.

 

Insulation:

Using two magnets and a paper towel, allow the magnets to connect through the paper towel. Repeat but this time fold the paper towel. Can the magnets still connect through the folded paper towel. Continue folding the paper towel until the magnets cannot connect. What have you demonstrated here?

 

Answer these questions in your lab report in the methods section as you are describing them. Remember to state the methods in a narrative form and not a numbered list.

  • What does the water inside the paper cup represent based on our lectures?
  • What kind of channel does the pin hole represent (be specific!!)?
  • What ion does the food coloring represent?
  • What does the paper towel represent?
  • What do the magnets represent?

 

Lab 3 – Part 2:

The knowledge you gained from the food coloring should help build your hypothesis about how a cell’s membrane potential is controlled by changes in the ion concentration. Form a hypothesis about what will happen as you decrease Na+ concentrations outside the cell. Remember this hypothesis as you will need it for the lab!

 

Next go to this Simulator for Neural Networks and Action Potentials (SNNAP) https://nba.uth.tmc.edu/neuroscience/s1/labs/actpot/hhsimu.html

by the University of Texas Health Science Center at Houston. You will land on a page showing the one below.

The blue line Vm represents the membrane potential that is calculated using this equation.

 

In order to understand anything about this equation you will need to know what the terms in the equation mean. As stated above, the Vm is the membrane potential, Cm is the membrane capacitance (capacitance is the ability of a membrane to store a charge and is determined by physical properties of the membrane), Iinj is the injected current, gNa is the Na+ conductance, gK is the K+ conductance, and gl is the leakage conductance. ENa and EK are the equilibrium potentials of sodium (Na) and potassium (K) respectively. There are also a few variables that model activation of ion channels. Recall that ion channels are what gives the membrane permeability to the ions. Ions themselves will not pass-through membranes. There had to be a hole in the cup to let the ions (dye molecules) out. The conductance of the Na+ channel is governed by an activation variable m and an inactivation variable h, gNa = gNamax m3h and the conductance of the K+ channel is governed by a single activation variable n, gK = gKmax n4

 

Causing and Action Potential with Channel Opening.

Now that we understand the terms, we can start manipulating some of them. The default settings here are set to use an electrical impulse (Current Injection) to trigger an action potential (blue line). The orange and green lines model the increase in permeability of sodium and potassium ions due to the opening of sodium and potassium channels due to an electrical impulse.  Notice that there is a term for Current Injection. This is the stimulus that will trigger the opening of the ion channels in the membrane because here we are modeling voltage gated ion channels. When you set this Current Injection to zero, there will be no permeability of the membrane to ions (all channels are closed).

 

Answer these questions in your results section.

  • What happens to the membrane potential when the Current Injection is zero?
  • Alter the Current injection to be 5 nA/cm2. Do you see an action potential being fired now?
  • Step up the Current Injection from 5 nA/cm2 one step at a time leaving all other parameters set to their default. At what current do you see the action potential fire?

Answer these questions in your results and discussion section.

  1. Knowing that Current Injection causes ion channels to open, explain what has happened when the current reaches the level needed to cause the action potential. Make sure to mention channels opening and increased permeability of ions.

 

Altering Ion Concentrations

We know from the Nernst and Goldman equations mentioned in the beginning of this lab that the equilibrium potential for ions can be simplified (over simplified) to a ratio of the concentration of an ion outside a cell to that on the inside of the cell [ion]outside/ [ion]inside. Mathematically this means that as the concentration of the ions outside a neuron is lowered so will the equilibrium potential of that ion. Reducing the concentration of sodium ions outside side of a neuron would mimic what happens in cases of hyponatremia (low sodium and too much water) that we saw in “The Agony of Ecstasy MDMA and the Kidney” paper.

 

Notice that you can also change Equilibrium potential of both sodium and potassium. In this exercise we will manipulate the equilibrium potential of sodium to model hyponatremia. When we reduce the equilibrium potential of sodium, we are effectively decreasing the amount of sodium outside the cell and breaking down the concentration gradient of sodium that exists across the neuron membrane. Recall that ions will move from areas of high concentration to areas of low concentration (flowing down the concentration gradient).

 

The default settings on our simulator models a standard sodium gradient that you would see under normal conditions. This results in an Equilibrium potential of sodium of 55 mV. To model hyponatremia, change this to 0 mV while keeping all other parameters the same.

 

Answer these questions in your results section.

  • Where you able to trigger an action potential while the equilibrium potential of sodium was zero? Note that the action potential trace is still in a dotted blue line so you can see what it would look like.
  • Note the membrane potential at the peak (apex of blue line) when the Equilibrium potential of sodium is 0 mV and check that it matches what is on the chart below. Determine the membrane potential at the peak for four more points of sodium equilibrium potential levels anywhere between zero and 55 and fill in the chart below.

 

Sodium Equilibrium Potential (mV) Membrane Potential (mV)
0 -41.5
   
   
   
   

 

For your graphics section.

  • Make a scatter plot of Membrane Potential vs. Sodium Equilibrium Potential. Since Sodium Equilibrium Potential is the independent variable it should go on the x-axis (Abscissa) and since the Membrane Potential is the dependent variable it should go on the y-axis (Ordinate). Add a trendline and determine the coefficient of determination (R2). For more information on the R2 and what it can tell us look here. What trend do you notice? How can you tell if it is significant?

 

In your discussion section answer the following.

  • Now let’s imagine a scenario like the one in the JAMA article about ““The Agony of Ecstasy MDMA …” where the sodium outside the neuron is really low and thus causing the equilibrium potential of sodium to be low. Based on your plot above do you think that action potentials (depolarization of the membrane) will be more difficult in hyponatremia?
  • How might this change in action potentials affect consciousness?
  • How might this change in action potentials affect your heart’s ability to beat?
  • Why does taking ecstasy sometimes result in this?

 

Lab 3 Write-up Rubric

 

Formatting (1 point):

  • (0.2 points) 12 point font in a standard font (such as Arial, Times, or Calibri)
  • (0.2 points) Single Spaced
  • (0.2 points) Separate page for graphics, figures, and references.
  • (0.2 points) Each section has a clear header.
  • (0.2 points) 1.5 Page minimum reached. It can be and easily will be longer.

 

Introduction (2 points): Introduce the lab and your hypothesis. Give pertinent background information as needed that explains what you are doing.

  • (0.5 points)Clear and strong hypothesis
  • (0.5 points)Background Information with in-text citations for all facts in APA style.
  • (0.5 points)Background information leads logically to your hypothesis.
  • (0.5 points)No information that should be in other sections (e.g., discussion).

 

Methods (1.5 points): Talk about what you did for the lab to collect the data and/or information as well as the analyses you did.

  • (0.5 points)Clear explanation of all steps take to collect the data with enough detail that someone could repeat the work. Copy and paste of the lab manual is not okay.  Make sure to answer the required questions as statements.
  • (0.5 points)Clear explanation steps taken to analyze any data. Copy and paste of the lab manual is not okay. This must be your own words.
  • (0.5 points)No information that should be in other sections (e.g., results).
  • This must be your own words in a narrative (not a list form). You will lose half of your points in this section if it is in a list and not a narrative form.

 

Results (1.5 points): Talk about the data you collected and the results of the analysis without analyzing it. Analysis means that you are telling us what the data and results means. For example, “this group was bigger than that one.” Just state the numbers and let the reader figure out which one is bigger on their own. Save the analysis for the discussion!

  • (0.5 points)All required results are stated/ submitted. For example if you calculated an average you state what that result was and these results make sense for the experiment. Make sure to answer the required questions as statements.
  • (0.5 points) Results written in paragraph form as a narrative.
  • (0.5 points)No conclusions of what the results mean or information that belongs in another section of the report. Note graphics like charts belong in the graphics section!

 

Discussion (2 points): Analyze the data in your results and relate that to your hypothesis. The discussion section will also be where you talk about  how to improve your research and why this type of study matters.

  • (0.5 points)Summary of what was found and why it matters. Make sure to answer the questions given in the lab report for this section.
  • (0.5 points)Clear statement of whether the hypothesis was supported or rejected and why.
  • (0.5 points)Statement(s) of what the strengths of the experimental approach were.
  • (0.5 points) Statement(s) of what the weaknesses of the experimental approach were including possible sources of error or bias.

 

References (1 point):

  • (0.5 points)You need to use one additional reference to the paper we have given here.
  • (0.5 points)References are reliable and valid sources. (e.g., pass the CRAAP test).

 

Graphics (1 point):

  • (0.5 points) Give a completed chart of your values from part 2 and an XY scatter plot of these values.
  • (0.5 points) Appropriate labels are provided for each graphic. This include chart titles and axis labels.

 

Provide an example of a fixed population and an example of a dynamic or open population. Explain the significance of each population type as related to the examples you provided.

Answer these epidemiology questions.

1.
a. Provide an example of a fixed population and an example of a dynamic or open population.
b. Explain the significance of each population type as related to the examples you provided.

2.Complete the following exercise correctly. Please refer to the Fact Sheet and MMWR Report to answer the questions.

We discussed the importance of defining the case during the lecture and reviewed the evolution of the case definition for HIV. The case definition for HIV infection was further revised in 2014. List and justify 3 attributes of the new definition in comparison to previous definitions based on information in the Fact Sheet: Terms, Definitions, and Calculations Used in CDC HIV Surveillance (December 2016) and the MMWR Report, April 11, 2014.
Direct link, Fact Sheet: https://www.cdc.gov/hiv/pdf/statistics/systems/nhbs/cdc-hiv-terms-surveillance-publications-2014.pdf Links to an external site.

Direct link, MMWR Report: http://www.cdc.gov/mmwr/preview/mmwrhtml/rr6303a1.htm?s_cid=rr6303a1_e Links to an external site.

3.You are studying hypertension among smokers and nonsmokers. We have 300 smokers,700 nonsmokers, 500 individuals with hypertension, and 500 without. There are 250 smokers with hypertension and 250 nonsmokers with hypertension. Create a 2×2 table with the above information and compare the incidence rate of smokers with hypertension and nonsmokers with hypertension.

Describe your impression of at least one of the speakers in 400-500+ words. Do you know someone who has seen this specialist, and how does it affect your viewpoint of this career?

Assignment – Reflective Writing – Meet the Experts: Pharmacy/Dentistry/Neurology & Women’s Health

  • Describe your impression of at least one of the speakers in 400-500+ words.
  • Do you know someone who has seen this specialist, and how does it affect your viewpoint of this career?
  • Would the hours that the doctor works fit within the lifestyle you wish to have, why?
  • How might this job fill the need for you to feel satisfied with your career?

Name and describe your species. It’s okay if you just call them “species I,” “species 2,” but each item must have a unique name.

Grocery Taxonomy Lab

Before beginning this exercise, be sure that you’ve studied Section 12.3 from your text. You may also find this web site to be useful: Classification of Living Things

Objective:

The point of this exercise is to help you understand the practice of taxonomy.

Materials:

An assortment of thirty different food items
A ruler, tape measure, or digital scale with metric units

Methods:

Hopefully, you will be able to rummage around in your kitchen to find 30 items to use for this lab. Try for variety and diversity in your selection. You may only use one of each specific item.
Your 30 objects represent members of thirty different species in the Kingdom Grocery. Your task is to organize your species into genera, families, and Orders in the manner of the Linnaean classification system.

First, carefully name and describe your species. It’s okay if you just call them “species I,” “species 2,” but each item must have a unique name. You should also measure each item in some way (using metric units) and include these measurements in your descriptions — length, diameter, circumference, weight, etc. You will need to create a word doc and type your 30 species names, descriptions, and measurements.

The system developed by Linnaeas has seven major levels of classification, beginning at the most general (most inclusive) level, Kingdom, and ending with the most specific, (least inclusive) species.

(Note: An additional level above Kingdom was added later).

Your items are all in the Kingdom Grocery. Your next task is to organize your 30 species into genera, genera into families and families into orders. Make sure your taxonomy nests properly and is clear to anyone who reads it.

HINT to help you get started:

Remember that Linnaeus decided on his classification by grouping species into genera because of physical similarity, then grouping genera into families because of broader similarity, etc. You might  find it easiest to begin at the most specific level and move toward the general. Spread your objects out and cluster them into categories based on similarities. Don’t forget, by the way, that each category (or taxon) has to have a name. Once you’ve got your species clustered into genera, then go on and cluster your genera into families, etc.

Show your nesting scheme either as a branching diagram or in outline view. For example, if I were making a nesting scheme for certain items of clothing, it might look like this:

  • Order Outerwear
  • Family Winter
  • Genus Hats
  • Species Striped Beanie
  • Species Red Stocking Hat

If you have any questions contact me

What is the rate of infertility of men and women ages 18-50 in the United States? What is the current contraceptive status amongst women ages 18-50 in the United States?

Replay to these 2 posts with more information

Post #1:
The National Survey of Family Growth collects data on a variety of categories such as pregnancy and births, marriage and cohabitation, infertility, use of contraception, family life, and general and reproductive health. The data is collected by conducting surveys and performing a statistical analysis on them. Some of the research questions that can be formed by using this data source are ,“What is the rate of infertility of men and women ages 18-50 in the United States,” and “What is the current contraceptive status amongst women ages 18-50 in the United States.” One hypothesis could be “Men and women who live in areas of high pollution tend to suffer from infertility more than men and women who do not.” Some strengths of the NSFG as a source of data on unintended pregnancy are its wealth of information on pregnancy, contraceptive use, and related topics. Some weaknesses included the questions as well as how they were interpreted by the respondents.

Reference

Qureshey, E. J., Chen, H. Y., Wagner, S. M., Chauhan, S. P., & Fishel Bartal, M. (2022). Factors associated with long-acting reversible contraception usage: Results from the National Survey of Family Growth. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 10.1002/ijgo.14485. Advance online publication. https://doi.org/10.1002/ijgo.14485

Post #2:
The Influenza Hospitalization Surveillance Network (FluSurv-NET) collects demographic and clinical data from patients that have laboratory-confirmed influenza-associated hospitalizations1.

Data collection usually runs from the start to the end of flu season each year (Oct 1 – April 30), though collection periods can and do change if there is atypical influenza activity in any given year. The data collected is generally used to calculate a weekly influenza-associated hospitalization rate, which is then reported to the CDC1.

Because FluSurv-NET collects demographic data, it is possible to examine specific demographics to determine if they have a higher risk of influenza-associated hospitalization.

As an example, a hypothesis that could be addressed using the data source would be: pregnant women are at higher risk of experiencing an influenza-associated hospitalization than the general population.

One strength of the data source is that it only includes laboratory-confirmed cases of influenza-associated hospitalizations. This removes any ambiguity as to whether the patient had influenza, as opposed to self-reporting. One weakness of the data source is that it only collects data from hospitals in 14 states. While the states are fairly well spread out, there is no guarantee that the data collected necessarily reflects national influenza-associated hospitalization rates1.

 

References

Centers for Disease Control and Prevention. (2023, January 17). Influenza hospitalization surveillance network (FLUSURV-net). Centers for Disease Control and Prevention. Retrieved January 29, 2023, from https://www.cdc.gov/flu/weekly/influenza-hospitalization-surveillance.htm