if you were to repeat the temperature experiment using pigmented animal cells, what absorbance values would you expect for each temperature? Why? (the original experiment tested the absorbance of tbe pigment from a beet sample in the spectrophotometer at 470 nm at -20 degrees celsius, 4 degrees C, 25 degrees C, 37 degrees C, 55 degrees C, and 80 degrees C

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Answer 1

If I were to repeat the temperature experiment using pigmented animal cells, the expected absorbance values for each temperature would differ because different pigments will respond differently to temperature.

As temperature increases, absorbance generally increases because it alters the structure of the pigments that absorb the light. It is therefore possible that the pigmented animal cells could show a different response at each temperature compared to the beet sample. The expected absorbance values would depend on the pigment's optimal temperature range and how it is affected by temperature changes.

In general, the rate of chemical reactions doubles with a 10°C increase in temperature, which means that the pigments in the animal cells could denature at higher temperatures, causing the absorbance to decrease. Lower temperatures, on the other hand, may lead to reduced absorbance due to lower kinetic energy and slower reaction rates.

In conclusion, the expected absorbance values for each temperature if I were to repeat the temperature experiment using pigmented animal cells would depend on the type of pigment and its optimal temperature range. The pigments could show different responses to temperature changes, and the optimal range for each pigment would be unique.

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Related Questions

Plant cells are connected by plasmodesmata, channels that permit the transport of ions and small molecules between the cells. Which of the following is the most closely analogous structure in a multicellular animal? a. The synapse between two neurons b. The aquaporins in cells of the descending limb of the loop of Henle in kidney nephrons c. The gap junction between two cardiac muscle cells d. The tight junction between two intestinal epithelial cells

Answers

The correct answer is the gap junction between two cardiac muscle cells. Explanation: Plant cells have connections that are unique from those found in multicellular animals. In plant cells, plasmodesmata are present, which are channels that enable ions and small molecules to be transported between cells.

It is the closest analogy to a multicellular animal structure that aids in the transport of ions and small molecules between cells. Gap junctions, which are specialized connections between cells in multicellular animals that allow direct cell-to-cell interaction, are the closest analogy to this plant structure.

Connexin proteins create the channels in these gap junctions, which transport ions and small molecules such as glucose and amino acids directly between two neighboring cells. This structure helps to synchronize contractions between two cardiac muscle cells in particular. So, the gap junction between two cardiac muscle cells is the most closely analogous structure in a multicellular animal to the plasmodesmata present in plant cells.

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illustrate the classifications of cytological methods in
detail.

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Cytological methods are techniques that are used in the laboratory for observing the cells of the living organism. The process involves the study of the cells under the microscope.



This is a type of light microscopy, which is used for observing the cells that are fixed to the slide. It is used to observe cells that are not stained, or cells that are stained with a basic dye such as hematoxylin. her specimens. Light microscopy can be used to observe living cells and tissues, and it can be used to detect cellular abnormalities. 2. Electron Microscopy: Electron microscopy is a technique that uses a beam of electrons to magnify the image of cells and other specimens.

This method is used to observe the cells that are living, and it helps to differentiate the cells that have a high refractive index. The cells that are living are differentiated from those that are dead. 
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ces During the flexion phase of a biceps curl, the elbow flexors are: O Contracting isometrically O Contracting concentrically O Contracting eccentrically Are not primarily involved in the movement

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During the flexion phase of a biceps curl, the elbow flexors are contracting concentrically.Concentric muscle contractions occur when the muscle shortens in length as it generates force, pulling on the bones to create movement. In contrast to concentric contractions,

eccentric muscle contractions occur when the muscle lengthens in response to an opposing force greater than the force generated by the muscle. Isometric contractions occur when the muscle generates force but does not change in length.

The elbow flexors are the primary movers during the flexion phase of a biceps curl. During this phase, the biceps muscle contracts concentrically to shorten and pull on the forearm bones to create movement. Thus, the main answer is Contracting concentrically.

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Choose any/all that apply to the citric acid cycle. One complete turn of the cycle generates three molecules of NADH, one molecule of FADH2 and two molecules of CO2. The rate of the citric acid cycle is increased in the presence of ATP. The oxidation of acetyl CoA provides the energy-rich electrons that are harvested in the citric acid cycle. The citric acid cycle requires aerobic conditions even though no O₂ is directly consumed in the reactions of the cycle. One complete turn of the cycle results in the consumption of one molecule of oxaloacetate. The rate of the citric acid cycle is increased in the presence of cyanide, a potent inhibitor of the electron transport chain.

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The statements that apply to the citric acid cycle are: One complete turn of the cycle generates three molecules of NADH, one molecule of FADH2, and two molecules of CO2. The oxidation of acetyl CoA provides the energy-rich electrons that are harvested in the citric acid cycle. The citric acid cycle requires aerobic conditions, even though no O₂ is directly consumed in the reactions of the cycle.

The citric acid cycle, also known as the Krebs cycle or the tricarboxylic acid cycle, is a central metabolic pathway that occurs in the mitochondria of eukaryotic cells. It plays a critical role in the oxidation of acetyl CoA, which is derived from carbohydrates, fats, and proteins. During one complete turn of the cycle, three molecules of NADH, one molecule of FADH2, and two molecules of CO2 are generated. These electron carriers (NADH and FADH2) carry energy-rich electrons that are later used in the electron transport chain to produce ATP.

The citric acid cycle requires aerobic conditions because it relies on the availability of molecular oxygen (O₂) as the final electron acceptor in the electron transport chain. Although O₂ is not directly consumed in the citric acid cycle reactions, its presence is necessary for the proper functioning of the electron transport chain.

The statement regarding the consumption of one molecule of oxaloacetate is incorrect. Oxaloacetate is regenerated during the cycle and is not consumed. The statement about the citric acid cycle being increased in the presence of cyanide, a potent inhibitor of the electron transport chain, is also incorrect. Cyanide inhibits the electron transport chain, thereby disrupting the production of ATP, and subsequently slows down the citric acid cycle as it relies on the electron transport chain for the re-oxidation of NADH and FADH2.

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The earlier the stage in immune development a genetic mutation occurs, the more likely that the mutation will affect immune development more profoundly. True or False?

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True. The earlier a genetic mutation occurs during immune development, the more likely it is to have a profound effect on immune development.

This is because immune development involves a complex and highly regulated series of events, including the development and differentiation of immune cells, the establishment of immune tolerance, and the recognition and response to pathogens.

Genetic mutations that occur early in immune development can disrupt these processes and lead to significant impairments in immune function.

During early stages of immune development, stem cells give rise to progenitor cells, which subsequently differentiate into various immune cell types, such as T cells, B cells, and natural killer cells. Mutations that occur during these early stages can disrupt the normal development and maturation of immune cells, leading to impaired immune responses.

These mutations can affect crucial steps in immune cell development, including the rearrangement of gene segments that encode antigen receptors, the selection of immune cells with appropriate receptor specificity, and the development of tolerance to self-antigens.

In contrast, mutations that occur later in immune development, after immune cells have matured and are functioning, may have a lesser impact on immune development.

While they can still cause specific defects or dysregulation in immune responses, they may not disrupt the overall process of immune development to the same extent as mutations that occur earlier.

It's important to note that the specific consequences of a genetic mutation on immune development can vary depending on the gene affected, the nature of the mutation, and other genetic and environmental factors.

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Imagine you are a researcher in New Delhi. You hear reports coming in that coronavirus patients in your area are presenting with a more severe form of the disease with extremely high rates of septicaemia (infection within the blood) and multiorgan failure. Both coronavirus and the bacteria Haemophilus influenzae have been isolated in the blood of some of these patients. It is your job to design a study to answer the following question: Is this more severe disease caused by a new variant of coronavirus, a new type of H. influenzae, or are both pathogens somehow involved? Design a clinical study that will collect and analyse samples to try to answer this question Describe the potential results of this study Discuss how the potential results help identifying the cause of severe symptoms

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To design a study to answer the question of whether the more severe disease caused by a new variant of coronavirus, a new type of H. influenzae, or both pathogens are somehow involved, a clinical study will be designed.

What is septicaemia?

Septicaemia is defined as blood poisoning caused by the presence of microorganisms or their toxins in the blood or other tissues of the body. In other words, it's a severe bacterial infection in the blood that can lead to organ failure.

What is multi-organ failure?

Multi-organ failure is a condition in which multiple organ systems in the body begin to fail due to an injury or illness.

What are the potential results of this study?

If the more severe disease is caused by a new variant of coronavirus, the study would find that patients who have this variant will develop a severe form of the disease and will have a high rate of septicaemia and multi-organ failure.

If it is caused by a new type of H. influenzae, the study would find that patients who have this type of bacteria in their blood would develop the same severe form of the disease.

If both pathogens are involved, the study would find that patients who have both pathogens would develop an even more severe form of the disease, which may lead to death or permanent damage to multiple organs in the body.

How do potential results help identify the cause of severe symptoms?

The potential results of the study will help to identify the cause of severe symptoms by determining which pathogen is causing the more severe form of the disease.

This information can be used to develop effective treatments and vaccines for the specific pathogen, which will help to reduce the severity of the disease and save lives.

Additionally, identifying the cause of the severe symptoms will help to prevent the spread of the disease by implementing effective control measures such as quarantine, contact tracing, and other infection control measures.

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What are the four nitrogenous bases of DNA? Adenine, Guanine, Uracil, Cytosine Adenine, Uracil, Thymine, Cytosine O None of the answers is correct. O Adenine, Guanine, Cytosine, Thymine

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The correct option is (D)The four nitrogenous bases of DNA are Adenine, Guanine, Cytosine, and Thymine.

Adenine forms two hydrogen bonds with Thymine, and Guanine forms three hydrogen bonds with Cytosine. These four bases are the building blocks of DNA.

DNA is the genetic material that carries hereditary information in living organisms. It is composed of four nitrogenous bases that are paired to form the rungs of the DNA ladder. The four nitrogenous bases of DNA are Adenine, Guanine, Cytosine, and Thymine.

These nitrogenous bases pair up to form base pairs.Adenine forms two hydrogen bonds with Thymine, and Guanine forms three hydrogen bonds with Cytosine.

These four bases are the building blocks of DNA. The order and sequence of these bases determine the genetic information encoded in DNA. Any change in the order of bases can cause mutations that can lead to diseases.

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Write a hypothesis related to this data
write any hypothesis related to assimilation efficiancy, change in
speed , % avg water composition which are dependant variables,
relation to the independant 1. Clearly state the research hypothesis (or hypotheses) you are investigating. This/these hypothesis/hypotheses are experimental The hypothesis does NOT have to be in the form of an IF, AND, THEN sta

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The research hypothesis suggests a significant relationship between assimilation efficiency, change in speed, and % avg water composition, influenced by an independent variable. The experimental hypothesis specifically focuses on the impact of increasing water temperature on these variables and proposes that temperature affects the relationship.

A hypothesis related to assimilation efficiency, change in speed, and % avg water composition can be as follows:

Research hypothesis: There is a significant relationship between assimilation efficiency, change in speed, and % avg water composition. This relationship is influenced by the independent variable (such as temperature, pH, or concentration of a nutrient).

Experimental hypothesis: Increasing the temperature of water increases the assimilation efficiency and change in speed of organisms in the water. The % avg water composition is also affected by temperature as it is a measure of the amount of water present in the sample. Therefore, the relationship between assimilation efficiency, change in speed, and % avg water composition is dependent on temperature.

This hypothesis can be tested through experiments where the temperature of the water is varied while keeping other factors constant. The assimilation efficiency and change in speed of organisms can be measured, and the % avg water composition can also be calculated. The results can then be analyzed to determine if there is a significant relationship between these variables and temperature.

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How do terminally-differentiated cell types contribute to a supportive niche environment for planarian neoblasts?
Is there a difference between potency and developmental potency?
What is the developmental potency of Archeocytes?

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Planarians are flatworms that have evolved a remarkable stem cell system. A single pluripotent adult stem cell type.

Called a neoblast, gives rise to the entire range of cell types and organs in the planarian body plan, including a brain, digestive, excretory, sensory, and reproductive systems. Neoblasts are abundantly present throughout the mesenchyme and divide continuously

Potency refers to the ability of a stem cell to differentiate into different cell types. Developmental potency refers to the potential of a cell to give rise to all the cell types of an organism during development.

Archeocytes are totipotent cells found in sponges that can differentiate into any cell type. They have the highest level of developmental potency

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Postsynaptic facilitation a) All of the the statements are true. Ob) affects all targets of the postsynaptic neurons equally. Oc) is spatial summation. Od) occurs when a modulatory neuron synapses on

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Postsynaptic facilitation occurs when a modulatory neuron synapses on the presynaptic terminal. So, option D is accurate.

Postsynaptic facilitation refers to the process where the postsynaptic response to a neurotransmitter release is enhanced. It occurs when a modulatory neuron synapses on the presynaptic terminal, leading to an increase in neurotransmitter release. This modulation can enhance synaptic transmission and influence the strength of the synaptic connection.

The other options are incorrect:

a) All of the statements are true: This is not accurate as the other options are not true.

b) affects all targets of the postsynaptic neurons equally: Postsynaptic facilitation can occur selectively at specific synapses and does not necessarily affect all targets equally.

c) is spatial summation: Spatial summation refers to the integration of signals from multiple presynaptic neurons at different locations on the postsynaptic neuron, which is different from postsynaptic facilitation.

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21] The most accurate estimation of VO2max is achieved from the HR response to a submaximal exercise test if several assumptions are met. Per that: A] What is a steady state HR and what is the procedu

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Steady-state HR refers to the HR that is achieved when an individual maintains a constant exercise workload for at least three minutes.

This steady state HR is considered to be representative of the body’s oxygen consumption (VO2) during exercise.The procedure for submaximal exercise test is to obtain a steady state HR response and maintain that HR for a period of at least 3 minutes while measuring HR, ventilation, and oxygen consumption.

The steady state HR is then used to estimate the VO2max.In order to obtain an accurate estimation of VO2max from the HR response to a submaximal exercise test, several assumptions must be met. These assumptions include:a. Steady-state HR must be achieved and maintained for at least 3 minutes.b. The relationship between HR and VO2 must be linear.

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You have 16 rare diploid yeast strains with which you want to perform this analysis. You put the two oligos (ASO#1 and ASO#2) on membranes (ASO#1 on the top row and ASO#2 on the bottom). You then extract genomic DNA from the yeast and PCR-amplify the DNA using primers that flank the AWA1 gene’s coding region. You label the PCR products with radioactivity and treat them chemically to make them single-stranded. You allow the labeled DNA to hybridize to the oligos, and you wash away any unbound DNA.
Predict the results for: strain 1 (homozygous for functional AWA1), strain 2 (heterozygous for functional AWA1 and awa1) and strain 3 (homozygous for awa1) by shading in the regions where you should see a hybridization signal below.

Answers

The analysis provided in the question uses a diploid yeast and involves a PCR-amplification of DNA.

Once the DNA is PCR-amplified, radioactivity is used to label the PCR products and treated chemically to make them single-stranded.

Subsequently, the labeled DNA is allowed to hybridize to the oligos, and any unbound DNA is washed away.

Homozygous for functional AWA1

In strain 1, which is homozygous for the functional AWA1 gene, it is expected that a hybridization signal will be present in the first row where the ASO#1 oligo is located, but not in the second row where ASO#2 is located.

you should see a hybridization signal in the top row of the membrane and no signal in the bottom row.

Heterozygous for functional AWA1 and awa1

For strain 2, which is heterozygous for functional AWA1 and awa1, hybridization signals should be visible in both rows of the membrane.


Homozygous for awa1

you should see a hybridization signal in the bottom row of the membrane and no signal in the top row.

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Evaluate the pulmonary pressures provided, and determine what portion of the respiratory pressure cycle is represented: Atmospheric pressure = 760 mmHg Intrapulmonary pressure= 763 mmHg Intrapleural p

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According to the information we can infer that intrapulmonary pressure = 763 mmHg represents forced inspiration.

What represents the intrapulmonary pressure?

Intrapulmonary pressure refers to the pressure inside the lungs. During forced inspiration, the diaphragm and other respiratory muscles contract more forcefully, causing an increase in lung volume.

This increased volume leads to a decrease in intrapulmonary pressure, creating a pressure gradient that allows air to flow into the lungs. The given value of 763 mmHg for intrapulmonary pressure is slightly higher than atmospheric pressure (760 mmHg), indicating that the pressure inside the lungs is slightly elevated during forced inspiration.

So, the provided intrapulmonary pressure of 763 mmHg represents forced inspiration.

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Which of the following would you NOT expect to see from a population that has experienced genetic drift
Group of answer choices
a.Isolated population with low levels of immigration
b.Low allelic diversity
c.High levels of heterozygosity
d.Small population size

Answers

c. High levels of heterozygosity. Genetic drift reduces genetic diversity over time. High levels of heterozygosity indicate a higher genetic diversity, which is not expected in a population that has experienced genetic drift.

Genetic drift refers to random changes in allele frequencies in a population due to sampling error. As a result, certain patterns emerge. While options a, b, and d are commonly associated with populations that have experienced genetic drift, option c, high levels of heterozygosity, is not expected. Genetic drift tends to reduce genetic diversity over time, resulting in lower levels of heterozygosity. Therefore, high levels of heterozygosity are more commonly associated with populations that have higher genetic diversity, such as those influenced by gene flow or natural selection. In the context of genetic drift, the effects are more pronounced in smaller populations where chance events can have a larger impact on allele frequencies.

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Which of these statements regarding secondary structure is FALSE? Al. Beta-strands are called an "extended" conformation because the side chains extend away from the strand axis. A2. In an alpha-helix, an H-bond forms between backbone atoms in amino acids that are actually more than two residues away from each other in the sequence. A3. The Ramachandran plot of a sheet will have most points in the upper-left region. A4. Unlike a DNA helix, a protein alpha-helix has side chains on the outside and backbone on the inside. AS. All of the above statements are actually true. p. 12 of 27 MBB 222 Summer 2022 W4-W5 - Exercises CQ4-22 (W5g Protein secondary structures) Which comparison / contrast statement is TRUE? A1. Alpha-helices and beta-strands have similar phi values but different psi values. A2. An alpha-helix and a parallel beta-sheet both have all C-O groups aligned in one direction. A3. Anti-parallel sheets have more H-bonds, making them more stable than parallel sheets. A4. H-bonds are formed between every 3-4 residues in an alpha-helix but between every 2 residues in a beta-strand. All of the above are truc. AS.

Answers

In an alpha-helix, an H-bond form between backbone atoms in amino acids that are actually more than two residues away from each other in the sequence is false regarding the secondary structure. Thus, A2 is correct. Anti-parallel sheets have more H-bonds, making them more stable than parallel sheets is true. Thus, A3 is correct.

A) The false statement regarding the secondary structure is A2. In an alpha-helix, an H-bond forms between backbone atoms in amino acids that are actually more than two residues away from each other in the sequence.

This statement is incorrect because in an alpha-helix, the H-bonds form between the carbonyl oxygen of one amino acid and the amide hydrogen of an amino acid four residues down the sequence. The helical structure allows for this regular pattern of H-bonding.

B) The true comparison/contrast statement is A3. Anti-parallel sheets have more H-bonds, making them more stable than parallel sheets. Anti-parallel beta-sheets have the strands running in opposite directions, allowing for more extensive H-bonding between the backbone atoms of adjacent strands.

This increased number of H-bonds enhances the stability of the anti-parallel sheets compared to parallel sheets, where the strands run in the same direction, leading to fewer H-bonds.

In conclusion, the false statement in the first question was A2, which inaccurately described H-bond formation in an alpha-helix. The true statement in the second question was A3, highlighting the greater stability of anti-parallel beta-sheets due to their increased number of H-bonds.

Understanding the characteristics and differences between secondary structure elements like alpha-helices and beta-sheets is crucial for comprehending protein folding, stability, and function. By examining these features, researchers can gain insights into the structural properties of proteins and their roles in various biological processes.

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3. Which of the following statements regarding the organization of the nervous system is NOT TRUE? A. The central nervous system coordinates all mechanical and chemical actions. B. The autonomic nervous system is under voluntary control. C. Somatic nerves control skeletal muscles, bones and skin. D. The spinal cord relays motor nerve messages from the brain to effectors. E. The peripheral nervous system consists of nerves that link the brain and spinal cord to the rest of the body. 4. Interneurons are most commonly associated with: A. sensory nerves. B. the central nervous system. C. the sympathetic nervous system. D. the peripheral nervous system. E. all of the above. A. 5. Which of the following sets of components are NOT a part of the reflex arc? Sensory receptor, spinal cord, effector Interneuron, motor neuron, receptor C. Sensory neuron, spinal cord, brain D. Spinal cord, motor neuron, muscle B. E. Receptor, interneuron, motor neuron 6. Which part of the neuron receives sensory information? a. dendrite c. axon b. sheath d. node of Ranvier e. cell body 7. Which part of the brain joins the two cerebral hemispheres? A. meninges D. cerebrum B. corpus callosum E. cerebellum C. pons

Answers

The autonomic nervous system is under voluntary control is NOT TRUE because the autonomic nervous system is involuntary and not under voluntary control. Interneurons are most commonly associated with . Hence option B is correct.

B. the central nervous system. Sensory neuron, spinal cord, brain are the sets of components that are NOT a part of the reflex arc because reflex arc comprises of Sensory receptor, interneuron, and motor neuron. The part of the neuron that receives sensory information is the dendrite. The dendrites receive chemical messages (neurotransmitters) from other neurons at their synapses. The cell body integrates information from the dendrites and sends out electrical signals via a specialized process known as the axon.

The corpus callosum joins the two cerebral hemispheres of the brain. It is a broad band of nerve fibers that connects the two hemispheres of the brain.

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The sides of a parallelogram measure 68 cm and 83 cm and one of
the diagonals measures 42 cm. Solve for the largest interior angle
of the parallelogram.

Answers

The largest interior angle of the parallelogram is approximately 136.96 degrees.

To find the largest interior angle, we can use the Law of Cosines. Let's denote the sides of the parallelogram as a = 68 cm and b = 83 cm. The diagonal is c = 42 cm. Using the Law of Cosines, we can solve for the angle opposite to the diagonal:

[tex]cos(A) = (b^2 + c^2 - a^2) / (2 * b * c)[/tex]

Plugging in the values, we get:

[tex]cos(A) = (83^2 + 42^2 - 68^2) / (2 * 83 * 42)cos(A) ≈ 0.3894[/tex]

Taking the inverse cosine (arccos) of this value, we find that A ≈ 136.96 degrees, which is the largest interior angle of the parallelogram.

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Two trays of cuttings are placed in different environments. Cuttings in Tray I are placed in dry air (40% humidity) whilst cuttings in Tray 2 are placed in moist air (95% humidity). Other factors being equal, which tray is likely to have a greater percentage of cutting survival? Give [2.5 Marks] two reasons.

Answers

Tray 2, which contains cuttings placed in moist air (95% humidity), is likely to have a greater percentage of cutting survival compared to Tray 1 (cuttings in dry air at 40% humidity). There are two reasons for this: Moisture Availability and Reduced Stress

1. Moisture Availability: Higher humidity in Tray 2 provides a more favorable environment for the cuttings. Cuttings rely on moisture for the process of root development and establishment. The increased moisture in Tray 2 helps to prevent excessive water loss through transpiration and provides a continuous supply of water to the cuttings, promoting their survival and root growth.

2. Reduced Stress: Dry air in Tray 1 (40% humidity) can lead to increased stress on the cuttings. Low humidity causes accelerated water evaporation from the leaf surfaces, resulting in water stress and dehydration for the cuttings.

This can hinder their ability to develop roots and establish themselves. In contrast, the higher humidity in Tray 2 reduces water stress and maintains a more favorable moisture balance for the cuttings, allowing them to focus on root growth and survival.

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True/False: 1. Bridge reaction produces 2ATP from one glucose 2. Krebs Cycle is also known as Citric Acid Cycle.

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The given statements are:1. Bridge reaction produces 2 ATP from one glucose. True. 2. Krebs Cycle is also known as Citric Acid Cycle. True.

1. Bridge reaction produces 2 ATP from one glucose. TrueThe transition reaction is also known as the Bridge reaction. It takes place in the mitochondrial matrix, where it converts two molecules of pyruvate that were formed during glycolysis to two molecules of acetyl-CoA. The reaction is catalyzed by pyruvate dehydrogenase and it is the link between glycolysis and Krebs Cycle. The reaction produces 2 ATP molecules.

2. Krebs Cycle is also known as Citric Acid Cycle. TrueThe Krebs Cycle is a series of chemical reactions that occur in the mitochondrial matrix in eukaryotic cells. It is also called the citric acid cycle or the tricarboxylic acid cycle. The cycle involves the oxidation of acetyl-CoA molecules that are produced by the bridge reaction and is the most important part of cellular respiration. The cycle also produces energy in the form of ATP and CO2. Hence, it is true that the Krebs Cycle is also known as Citric Acid Cycle.

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A mutation in the sequence below occurs: TTC-TGG-CTA-GTA-CAT After the mutation, the sequence has now changed to: ATC-TGG-CTA-GTA-CAT What type of mutation has occurred?

Answers

This is a point mutation, similar to a deletion mutation, it changes a few or just one single nucleotide in a codon.

Part 1: 2n=10. A gamete has ______ chromosomes.
Part 2: 2n=10. A gamete has ______ DNA molecules.
Part 3: 2n=10. A product of meiosis II has _____ chromosomes.
Part 4: A product of meiosis II has _____ DNA molecules

Answers

The gamete has 5 chromosomes. A gamete has 10/2 = 5 DNA molecules . Each of the four daughter cells produced has 5 chromosomes.

Part 1: If 2n=10, this means the diploid number is 10, and it is the total number of chromosomes in the somatic cell of the organism. This number can be divided in half to obtain the haploid number of chromosomes that can be found in gametes. Therefore, in this case, the gamete has 5 chromosomes.

Part 2: When it comes to the DNA molecules found in a gamete, it is important to note that DNA replication only occurs once during interphase before meiosis I. The sister chromatids produced by DNA replication are held together by a centromere, which means that a gamete has only half the number of DNA molecules found in a somatic cell. Thus, if 2n=10, a gamete has 10/2 = 5 DNA molecules.

Part 3: The end result of meiosis II is four haploid daughter cells, each with half the number of chromosomes of the parent cell. The parent cell had two sets of chromosomes (2n), so it had 10 chromosomes. During meiosis I, the chromosome number was reduced from 2n to n (5 in this case), and during meiosis II, sister chromatids were separated. As a result, each of the four daughter cells produced has 5 chromosomes.

Part 4: As mentioned in part 2, a gamete has half the number of DNA molecules found in a somatic cell. During meiosis II, the sister chromatids produced in meiosis I are separated into four haploid daughter cells. Each daughter cell inherits half the number of chromosomes of the parent cell and thus half the number of DNA molecules. Therefore, a product of meiosis II has 5/2 = 2.5 DNA molecules, but since DNA cannot be divided in half, the answer should be rounded to 3.

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Explain the importance of lipid nanoparticle technology in RNA delivery system.

Answers

Lipid nanoparticle technology plays a crucial role in RNA delivery systems, enabling efficient and targeted delivery of RNA therapeutics.

Lipid nanoparticle technology is of paramount importance in the field of RNA delivery systems. These nanoparticles, composed of lipids, are designed to encapsulate and protect RNA molecules, ensuring their stability and preventing degradation. The main answer lies in their ability to facilitate efficient and targeted delivery of RNA therapeutics to specific cells or tissues in the body.

Lipid nanoparticles possess unique characteristics that make them ideal for RNA delivery. Firstly, their small size allows for easy penetration through biological barriers, such as cell membranes. This enables effective delivery of RNA molecules into the target cells, where they can exert their therapeutic effects. Additionally, the lipid-based structure of these nanoparticles enables them to interact with cell membranes, facilitating the internalization of the RNA cargo into the cells.

Moreover, lipid nanoparticles offer protection to the RNA molecules during circulation in the body. The lipid bilayer of the nanoparticles shields the RNA from enzymatic degradation and clearance by the immune system. This enhances the stability and half-life of the RNA therapeutics, increasing their efficacy and reducing the required dosage.

Furthermore, lipid nanoparticle technology allows for precise targeting of specific cells or tissues. By modifying the surface of the nanoparticles with ligands or antibodies that recognize cell-specific receptors, researchers can achieve selective delivery of RNA therapeutics to the desired cells. This targeted approach enhances the therapeutic efficiency and minimizes off-target effects, improving the safety profile of RNA-based therapies.

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Question 2
2.1 Briefly discuss fihe principle of common intermediates (i.e. reaction coupling) in bioenergetics (4). Use an example
(6)
2.2 Present a schematic representaion of free energy changes for an energetically favourable reaction, showing the
effects of a catalyst
NE
Question 3
3. List the 6 assumptions by Henri and Michaels-Menten in describing the relationship between initial velocity and
substrate concentration versus the Briggs-Haldene modifications of the Michaelis-Menten equation
(12)
3.2 Present a schematic representation of the Lineweaver-Burk Plot and equation
(3)
Question 4
2.1 Classify enzyme reversible inhibitors by (a) giving the type, mechanism and etlect on the kinetic parameters (Km and
(10))
/max)
Question 4
Present the cleland notation for a ping-pong bi-b1 mechanIsm

Answers

The questions provided cover various topics in bioenergetics and enzyme kinetics. They address concepts such as common intermediates in bioenergetics, the Michaelis-Menten equation and its assumptions, enzyme inhibitors and their effects on kinetic parameters, and the Cleland notation for a ping-pong bi-bi mechanism.

1. The principle of common intermediates, also known as reaction coupling, plays a crucial role in bioenergetics. It refers to the linking of energetically unfavorable reactions with energetically favorable reactions through shared intermediates. By coupling these reactions, the overall free energy change becomes more favorable, allowing the unfavorable reaction to proceed. For example, in cellular respiration, the energy released during the oxidation of glucose is coupled with the synthesis of ATP through common intermediates like NADH and FADH2.

2. The schematic representation of free energy changes for an energetically favorable reaction shows the effect of a catalyst. A catalyst increases the rate of reaction by lowering the activation energy barrier. In the schematic, the presence of a catalyst results in a lower activation energy, enabling the reaction to occur more readily. This leads to a shift in the energy profile, with a lower energy barrier and a faster rate of reaction.

3. The six assumptions made by Henri and Michaelis-Menten in describing the relationship between initial velocity and substrate concentration are: 1) The enzyme-substrate complex forms reversibly, 2) The rate-determining step is the breakdown of the enzyme-substrate complex, 3) The total enzyme concentration remains constant, 4) The reaction is carried out under steady-state conditions, 5) The reaction is homogeneous, and 6) The substrate concentration is much higher than the enzyme concentration. The Briggs-Haldane modifications of the Michaelis-Menten equation introduced additional assumptions to account for inhibitor effects.

4. Enzyme reversible inhibitors can be classified into different types based on their mechanism and effects on kinetic parameters such as Km and Vmax. Types of reversible inhibitors include competitive inhibitors (compete with the substrate for the active site), uncompetitive inhibitors (bind to the enzyme-substrate complex), and mixed inhibitors (bind to both the enzyme and the enzyme-substrate complex). Competitive inhibitors increase the apparent Km value, while uncompetitive inhibitors decrease both the Km and Vmax values. Mixed inhibitors can either increase or decrease the Km value, depending on their affinity for the enzyme or enzyme-substrate complex.

the detailed principles of common intermediates in bioenergetics, the Michaelis-Menten equation and its assumptions, enzyme inhibitors and their effects on kinetic parameters, and the Cleland notation for a ping-pong bi-bi mechanism. These concepts are important in understanding the dynamics of biochemical reactions and enzyme kinetics.

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In which region of the stress-strain curve are tissue changes considered to result in permanent structural changes? Select one: O a. initial force O b. plastic O c. yield point O d. elastic

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In the plastic region of the stress-strain curve, tissue changes are considered to result in permanent structural changes. This region occurs after the elastic region and beyond the yield point. The correct answer is: b. plastic

In the plastic region, the material or tissue undergoes deformation even after the applied stress is removed. The deformation is not fully recoverable, and the material retains a new shape or structure.

The initial force, elastic region, and yield point are all part of the stress-strain curve but do not represent permanent structural changes. The initial force is the beginning of the curve where the material starts to deform. The elastic region represents reversible deformation, meaning the material returns to its original shape once the stress is removed. The yield point is the point at which the material begins to exhibit plastic deformation and permanent changes occur. The correct answer is: b. plastic

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why do pathogens have avirulence genes except preventing the
infection?

Answers

Pathogens have avirulence genes to evade or manipulate the host immune response, increase their chances of survival and replication within the host, and establish a successful infection.

Avirulence genes, also known as avr genes, encode specific factors or molecules that are recognized by the host immune system and trigger a defense response. Pathogens evolve avirulence genes as a means to manipulate or evade the host immune system, allowing them to establish an infection and survive within the host. By expressing avirulence factors, pathogens can modulate the host immune response, suppress immune defenses, or evade recognition by host defense mechanisms. This enables the pathogen to persist and replicate within the host, leading to successful infection. Avirulence genes play a crucial role in the complex host-pathogen interaction and can determine the outcome of the infection, including the severity of the disease and the pathogen's ability to colonize and spread within the host.

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Explain the reabsorption of glucose in the PCT by secondary active
transport. What determines the maximum rate at which glucose can be
reabsorbed by this transport process? Of what clinical significan

Answers

The reabsorption of glucose in the proximal convoluted tubule (PCT) occurs through secondary active transport. The maximum rate of glucose reabsorption is determined by the number of functional SGLTs and the concentration gradient of sodium.

The reabsorption of glucose in the proximal convoluted tubule (PCT) is an essential process in the kidneys to maintain glucose homeostasis. Glucose is filtered from the blood in the glomerulus and enters the PCT. To be reabsorbed back into the bloodstream, glucose utilizes secondary active transport, specifically a co-transport mechanism. This process involves the activity of sodium-glucose co-transporters (SGLTs) located on the luminal membrane of the PCT cells.

SGLTs are responsible for coupling the movement of sodium ions and glucose molecules. As sodium ions move down their concentration gradient from the lumen into the PCT cells via facilitated diffusion through sodium channels, they carry glucose molecules along with them against their concentration gradient. This co-transport process allows glucose to be reabsorbed from the tubular fluid into the PCT cells.

The maximum rate at which glucose can be reabsorbed by this transport process is influenced by two factors. Firstly, the number of functional SGLTs on the luminal membrane determines the capacity for glucose transport. If there are more SGLTs available, a higher number of glucose molecules can be transported. Secondly, the concentration gradient of sodium ions between the tubular fluid and the PCT cells affects the driving force for glucose reabsorption. A higher sodium concentration gradient provides more energy for the co-transport of glucose.

The clinical significance of this process lies in conditions where the reabsorption of glucose is impaired. For example, in individuals with uncontrolled diabetes mellitus, the glucose concentration in the blood can exceed the capacity of the SGLTs for reabsorption, leading to glucose being excreted in the urine (glycosuria). Monitoring the reabsorption of glucose in the PCT can help diagnose and manage diabetes mellitus and other renal disorders.

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Suppose that you have one wild-type female fly and one white-eyed male fly. What steps would you follow to produce a white-eyed female fly? Illustrate your with Punnett squares. A steps

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In order to produce a white-eyed female fly with one wild-type female fly and one white-eyed male fly, you would need to follow the following steps. This cross will result in all male progeny with wild-type eyes and all female progeny with white eyes.

There are two different ways to do this: Method 1: Cross a white-eyed male with a wild-type female The cross between a white-eyed male and a wild-type female will result in only male progeny with white eyes and female progeny with wild-type eyes.

This cross will result in all male progeny with wild-type eyes and all female progeny with white eyes. Punnett square for this cross: Note that since this cross involves an X-linked trait, only the female progeny will inherit the trait.

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What are ROS and examples of ROS? How do they affect the cells
resulting in aging?

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ROS stands for Reactive Oxygen Species, which are chemically reactive molecules containing oxygen.

They are natural byproducts of cellular metabolism and are generated during normal physiological processes such as aerobic respiration. Examples of ROS include superoxide anion (O2•-), hydrogen peroxide (H2O2), and hydroxyl radical (•OH).

While ROS play important roles in cellular signaling and defense against pathogens, excessive accumulation of ROS can have detrimental effects on cells. ROS can damage cellular components such as proteins, lipids, and DNA through oxidative stress.

This oxidative damage can lead to cellular dysfunction, impaired cellular signaling pathways, and ultimately contribute to aging and age-related diseases.

ROS-induced damage to DNA can result in mutations and genomic instability, leading to impaired cellular function and increased risk of aging-related diseases such as cancer. ROS can also promote inflammation and activate signaling pathways involved in cellular senescence, a state of irreversible cell cycle arrest associated with aging.

To counteract the negative effects of ROS, cells have antioxidant defense systems that include enzymes such as superoxide dismutase, catalase, and glutathione peroxidase. These enzymes help neutralize ROS and maintain cellular redox balance. However, with age, the efficiency of these defense mechanisms may decline, leading to increased ROS accumulation and subsequent cellular damage, contributing to the aging process.

Overall, the balance between ROS production and antioxidant defense systems is crucial for maintaining cellular homeostasis and preventing age-related cellular dysfunction and aging-associated diseases.

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Where are the internal nares located? Between the nasal cavity and the nasopharynx Between the glottis and the epiglottis Between the oropharynx and the oral cavity O Between the trachea and the prima

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The internal nares, also known as the internal nostrils or choanae, are located between the nasal cavity and the nasopharynx.

What are the internal nares?

The internal nostrils, or choanae, are paired openings located at the back of the nasal cavity. They connect the nasal cavity to the nasopharynx, which is the upper part of the throat. These openings allow for the passage of air and facilitate the flow of air from the nasal cavity into the respiratory system.

They serve as the opening through which air passes from the nasal cavity into the back of the throat (nasopharynx) and eventually into the respiratory system.

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Enterobacteriaceae Identification: The EnteroPluri-Test System (continued) B. Short-Answer Questions 1. What are the advantages and disadvantages of multitest systems for bacterial identification? 2. Before using the EnteroPluri-Test System, what test must be performed to confirm the identity of your unknown as a member of the family Enterobacteriaceae? What is the expected result?

Answers

Multitest systems are beneficial for bacterial identification. Still, they do have their disadvantages too.

The advantages and disadvantages of multitest systems for bacterial identification are given below:

Advantages:

Multitest systems are easy to use, have low cost, rapid, and require minimal training and expertise. Multitest systems are designed to identify specific bacterial species or groups within a single test.Multitest systems help to reduce the time required to identify bacteria.

Disadvantages:

Some multitest systems lack specificity and may be misinterpreted or generate false-positive results.Sometimes, the tests are inaccurate, and they may not always work correctly.Multitest systems are costly, and the equipment may not be available to all users.   Before using the EnteroPluri-Test System, you must confirm the identity of your unknown as a member of the family Enterobacteriaceae. The IMViC test is used to differentiate Enterobacteriaceae from other bacterial families. The test consists of four different tests that help to identify bacteria.

The four tests are:

Indole production test Methyl Red test Voges-Proskauer test Citrate utilization test Indole production test:

The presence of indole in the tryptophan broth indicates a positive result, and the absence of indole indicates a negative result. Methyl Red test: Methyl Red is a pH indicator that turns red when the pH is below 4.5. A positive result is given when the pH indicator turns red. A negative result is given when the pH indicator remains yellow.Voges-Proskauer test: This test is based on the ability of certain bacteria to produce acetoin from glucose.

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An embryo exposed to a new teratogen caused all the ectoderm cells to be stuck at the dorsal surface of the embryo. The most likely explanation for this would beThat teratogen activated migrationThe teratogen prevented cleavageThe teratogen prevented cell divisionThe teratogen blocked epiboly Which type of risk is based on the financial integrity of a bond issuer? liquidity risk call risk business risk interest rate risk A thick-walled cylinder made of a material with yield strength of 500 MPa with 50 mm inner radius and 60 mm outer radius is subjected to an internal pressure of 60 MPa. Determine the reserve of plasticity based on Tresca theory. 21 MPa 6 MPa 17 MPa 15 MPa 10 MPa 12 MPa Problem # 1 [35 Points] Vapor Compression Refrigeration System Saturated vapor enters the compressor at -10oC. The temperature of the liquid leaving the liquid leaving the condenser be 30oC. The mass flow rate of the refrigerant is 0.1 kg/sec. Include in the analysis the that the compressor has an isentropic efficiency of 85%. Determine for the cycle [a] the compressor power, in kW, and [b] the refrigeration capacity, in tons, and [c] the COP. Given: T1 = -10oC T3 = 30oC nsc = 85% Find: [a] W (kW) x1 = 100% m = 0.1 kg/s [b] Q (tons) [c] COP Schematic: Process Diagram: Engineering Model: Property Data: h1 = 241.35 kJ/kg h2s = 272.39 kJ/kg h3 = 91.48 kJ/kgProblem # 2 [35 Points] Vapor Compression Heat Pump System Saturated vapor enters the compressor at -5oC. Saturated vapor leaves the condenser be 30oC. The mass flow rate of the refrigerant is 4 kg/min. Include in the analysis the that the compressor has an isentropic efficiency of 85%. Determine for the cycle [a] the compressor power, in kW, and [b] the heat pump system capacity, in kW, and [c] the COP. Given: T1 = -5oC T3 = 30oC nsc = 85% Find: [a] W (kW) x1 = 100% x3 = 0% m = 4.0 kg/min [b] Q (kW) [c] COP Schematic: Process Diagram: Engineering Model: Property Data: h1 = 248.08 kJ/kg h2s = 273.89 kJ/kg h4 = 81.9 kJ/kgProblem # 3 [30 Points] Gas Turbine Performance Air enters a turbine at 10 MPa and 300 K and exits at 4 MPa and to 240 K. Determine the turbine work output in kJ/kg of air flowing [a] using the enthalpy departure chart, and [b] assuming the ideal gas model. Given: Air T1 = 300 K T2 = 240 K Find: w [a] Real Gas P1 = 10 MPA P2 = 4 MPa [b] Ideal Gas System Schematic: Process Diagram: Engineering Model: Property Data: ______T A-1 _____T A-23 __ Figure A-4 MW = 28.97 kg/kmol h1* = 300 kJ/kg h1/RTc = 0.5 Tc = 133 K h2* = 240.2 kJ/kg h2/RTc = 0.1 Pc = 37.7 bar R = 8.314 kJ/kmolK Materials are isotropic and homogenous. No need of worrying about safety factors. 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