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what was the driving force for the development of microscale testing
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- Which of the following types of data produce curves similar in shape to the graph? Select all that apply 1.Bacterial growth in a culture 2.A normal distribution of height in a population of students 3.Exponential population growth 4.Haemoglobin binding of oxygen 5.Log transformations of drug dose curves 6.Osmotic fragility of red blood cells 7.A standard curve for an enyme assayI need assistance with how to read Fletcher Munson graphs. Please help and show me the proper way to analyze these graphs. The previous experts I've asked on this platform were incorrect.Methods should be 4-5 paragraphs long. Describe the exact set-up of the experiment to a Brassica rapa plant for a lighting experiment with natural sunlight and artificial lighting including how many plants you started with, what the seeds were planted in, if anything was added to the environment, etc. Describe in detail how to measure the Brassica rapa. Describe the variables that were held constant. Specifically, address the difference between the control groups versus experimental groups and how exactly you applied an independent variable which is the duration of light exposure of the Brassica rapa to the experimental group members. Quantify the independent variable.
- Explain each four steps in Product Development that was given below: a.) Isolation of microbes that produce product of interest. b.) Screening for best producing strain;naturally or mutation or genetic engineering c.)Optimization of production condition d.)Scaling up from lab scale ( up to 10L) to industrial scale (> 10,000L)There are different types of sampling designs that may be used depending on the types of studies. Which sampling design you may recommend for the following experiments : a. To investigate the disease incidence in a field of tomato b. To investigate the nosocomial infection in people c. To investigate the microbial diversity in an agricultural fieldWhat are advantages and disadvantages of solid phase bioremediation technique?
- "RESEARCH CONCEPT NOTE" INSTRUCTIONS: 1. Select and read peer-reviewed research articles online. Choose ONE recent article (2010-2022 only). These articles should focus on Microscopy, Cell Culture and Aseptic Technique, and Cell Counting. 2. Based on the research articles you have been reading, identify a SMART research problem/question, objective, significance, and methodology. Note: SMART- Specific, Measurable, Attainable, Realistic, and Time-bound. 3. Fill up the Concept Note Template below. TITLE: Background of the Problem/Question(2 paragraphs only) Research Problem (Gap)/Question(1 sentence only) Research Objectives(2-3 objectives only) Significance of the Proposed Solution(1-2 sentences only) Summary of Methodology(1-2 paragraphs only) ReferencesList all the references mentioned in the in-text citation. Follow APA format.Multitest systems use a series of miniaturized biochemical tests to determine the identity of an unknown organism. Compared to using individual test tubes for these same tests, multitest systems __________. Multitest systems use a series of miniaturized biochemical tests to determine the identity of an unknown organism. Compared to using individual test tubes for these same tests, multitest systems __________. are more resistant to contamination use less media and reagents require a shorter incubation period generate results that are easier to interpretRecall that while FOVS will change with changing objectives, the size of the organism itself does not change. Consider the next example. Example #1 Polyp Objective: 40x Example #2 Polyp blObjective: 10x Example #3 Polyp Objective: 4x Field of view: 500 µm Field of view: 2000 µm Field of view: 5000 µm Estimated # of Estimated # of Estimated # of organisms that fit organisms that fit organisms that fit across the FOV: 1 Approximate size of organism: 500μm/ 1 = 500 μm across the FOV: 4 across the FOV: 10 Approximate size of organism: 2000µm/ 4 = 500 µm Approximate size of organism: 5000μm/ 10-500 μm %3D The three examples above are of the same jellyfish polyp, but at varying objectives. What is the size of the polyp at the 40x objective? 10x? 4x? Which objective visualizes the polyp best? Which objective would be best used to estimate organism size with?
- How about the top two reasons why layering procedures should be used? Provide evidence by citing particular cases.Article - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501646/ Here are the articles provided within the question - They are not needed but are available if additional information is warranted - The figures being mentioned are already provided. This is Biochemoistry, please answer each part to the best of your ability. There are a max of 3 parts due to guidelines and please answer each part with clear and efficient work with answers. Thank youwhat are some of the strengths and weaknesses to using a Culture dependent enumeration approach from a microbial perspective