All DNA polymerases require a primer with a 3¢ OH group to begin DNA synthesis. The primer is a. a free DNA nucleotide.
b. a short stretch of RNA nucleotides.
c. a 3¢ OH group that is part of the primase enzyme.

Answers

Answer 1

All DNA polymerases require a primer with a 3' OH group to begin DNA synthesis. The primer is a short stretch of RNA nucleotides.  

The synthesis of DNA during replication requires a free 3′-OH group before the addition of the next nucleotide can occur. This is a problem because in DNA, the nucleotides are joined together by a phosphate group linking the 5′ carbon on one nucleotide with the 3′ carbon on another nucleotide.The enzyme that performs this essential step is called primase, which is a type of RNA polymerase. Primase synthesizes a short RNA primer that is complementary to a single-stranded section of DNA.A primer is a small RNA molecule (or sometimes a DNA molecule) that acts as a starting point for DNA synthesis.

The primer provides a free 3′-OH group to which a DNA nucleotide can be added. DNA polymerase can only add new nucleotides to an existing strand of DNA, it cannot start from scratch. Therefore, DNA polymerase requires a primer with a free 3′-OH group to begin DNA synthesis. All DNA polymerases require a primer with a 3′-OH group to begin DNA synthesis. This primer is a short stretch of RNA nucleotides.

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Nol yet answered Which of the following statements describes a difference between gametogenesis in males and females? Marked out of 0.50 Remove flag Select one: 1. Synaptonemal complexes are only formed in females, 2. Mitotic division of germ-cell precursors occur only in males: 3. Meiosis in females begins in the fetus, whereas male meiosis does not begin until puberty 4. Oocytes don not complete mitosis until after fertilization, whereas spermatocytes complete mitosis before mature sperm are formed estion 2 tot yet nswered A non-disjunction is caused by a failure of chromosomes to separate properly during meiosis. Which non-disjunction listed below will cause (in 100% of cases) death of the zygote in the womb? arked out of 00 Select one Flag estion a. Three copies of chromosome 1 b. Two copies of the Y chromosome c. Three copies of chromosome 21 d. Two copies of the X chromosome

Answers

Gametogenesis in males and females have significant differences.

These differences are highlighted below:

Meiosis in females begins in the fetus, whereas male meiosis does not begin until puberty:

Male and female gametogenesis begin at different stages of development.

Female meiosis begins in the fetus before birth, while male meiosis does not begin until puberty.

Oocytes don not complete mitosis until after fertilization, whereas spermatocytes complete mitosis before mature sperm are formed:

This difference between gametogenesis is related to the physical differences between the female and male germ cells.

The oocyte is the largest cell in the body, and it must remain dormant until it is fertilized by the sperm, while spermatocytes can complete mitosis before forming mature sperm.

Synaptonemal complexes are only formed in females:

This statement is false.

Synaptonemal complexes are formed by both male and female germ cells.

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Which best describes how we understand othersâ actions and movements?
a. When we mimic behavior, we observe the action and compute goals and intentions of the actor, and then reproduce the action based on the goal
b. When we mimic behavior, we learn what the intention of another is by performing the same action ourselves
c. When we imitate behavior, we learn what the intention of another is simply by performing the same action ourselves
d. When we imitate behavior, we observe the action and compute the goals and intentions of the actor, and then reproduce the action based on the goal

Answers

The best option that describes how we understand other's actions and movements is "When we mimic behavior, we observe the action and compute goals and intentions of the actor, and then reproduce the action based on the goal."

When we try to understand others' actions and movements, we attempt to mimic their behavior. We observe the action and calculate the goals and intentions of the actor, and then reproduce the action based on the goal. This helps us learn about the intentions of another person. In the case of imitation, we learn what the intention of another person is simply by performing the same action ourselves.

This is an incorrect statement since copying another person's action alone may not necessarily give us information about the actor's intention. Based on studies conducted, it is revealed that we understand the goals and intentions of others by utilizing our own motor system, in addition to tracking the gaze of the individual whose behavior we are observing.

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a. Draw two separate flow charts (one for lower temperatures
and another for increased temperatures). Show the homeostatic
responses that occur for each (including both physiological and
behavioral re

Answers

Homeostasis is the ability of the body to maintain a stable internal environment even in the presence of a constantly changing external environment.

The body regulates various physiological processes such as temperature, blood sugar levels, water balance, and others.

A change in the external environment can cause a deviation from the normal range of these processes, leading to physiological and behavioral responses to maintain balance.

Lower temperatures flow chart:

Behavioral responses:

shivering, curling up, seeking warmth.

Physiological responses: the body constricts blood vessels to the skin to reduce heat loss; increases metabolic rate to produce more heat;

release of hormones such as adrenaline and noradrenaline.Increased temperatures flow chart:

Behavioral responses:

sweating, moving to a cooler environment.

Physiological responses:

the blood vessels to the skin dilate to release heat; the sweat glands produce sweat, which cools the body; the respiratory rate increases to release heat through breathing.

Homeostasis is the body's ability to maintain a stable internal environment, even in the presence of a constantly changing external environment.

In the case of low temperatures, the body responds by shivering, curling up, seeking warmth, constricting blood vessels to the skin to reduce heat loss, increasing metabolic rate to produce more heat, and releasing hormones such as adrenaline and noradrenaline.

On the other hand, in high temperatures, the body responds by sweating, moving to a cooler environment, dilating blood vessels to the skin to release heat, producing sweat, which cools the body, and increasing the respiratory rate to release heat through breathing.

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SLC Activity #2 for Biology 1406 Name Mendelian Genetics Problems 1) A true-breeding purple pea plant was crossed with a white pea plant. Assume that purple is dominant to white. What is the phenotypic and genotypic ratio of the F1 generation, respectively? b. 100% purple; 100% PP a. 100% white; 100% Pp c. 50% purple and 50% white; 100% Pp d. 100% purple; 100% Pp e. 50% purple and 50% white; 50% Pp and 50% pp 2) A heterozygous purple pea plant was self-fertilized. Assume that purple is dominant to white. What is the phenotypic and genotypic ratio of the progeny of this cross, respectively? a. 50% purple and 50% white; 25% PP, 50% Pp, and 25% pp b. 100% purple; 25% PP, 50% Pp, and 25% pp c. 100% purple; 50% Pp, and 50% pp d. 50% purple and 50% white; 25% PP, 50% Pp, and 25% pp. e. 75% purple and 25% white; 25% PP, 50% Pp, and 25% pp. 3) A purple pea plant of unknown genotype was crossed with a white pea plant. Assume that purple is dominant to white. If 100% of the progeny is phenotypically purple, then what is the genotype of the unknown purple parent? What special type of cross is this that helps identify an unknown dominant genotype? 4) A purple pea plant of unknown genotype was crossed with a white pea plant. Assume that purple is dominant to white. Of 1000 offspring, 510 were purple, and 490 were white; the genotype of the unknown purple parent must be: 5) Yellow pea color is dominant to green pea color. Round seed shape is dominant to wrinkled to wrinkled seed shape. A doubly heterozygous plant is self-fertilized. What phenotypic ratio would be observed in the progeny? A) 1:1:1:1 B) 9:3:3:1 C) 1:2:1:2:4:2:1:2:1 D) 3:1 E) 1:2:1 6) What is the genotype of a homozygous recessive individual? a. EE c. ee b. Ee 7) Red-green color blindness is. X-linked recessive trait. Jane, whose father was colorblind, but is normal herself has a child with a normal man. What is the probability that the child will be colorblind? A) 1/2 B) 1/4 C) 1/3 D) 2/3 8) Red-green color blindness is an X-linked recessive trait. Jane, whose father was colorblind, but is normal herself, has a child with a normal man. What is the probability that a son will be color- blind? A) 1/2 B) 1/4 C) 1/3 D) 2/3 9) Flower color in snapdragons is an example of incomplete dominance. A pure-breeding red plant is crossed with a pure-breeding white plant. The offspring were found to be pink. If two pink flowers are crossed, what phenotypic ratio would we expect? a. 1 Red: 2 Pink : 1 White b. 3 Red: 1 Pink c. 3 Red: 1 White d. 1 Red: 1 Pink

Answers

The answers to the biology 1406 name mendelian genetics problems are as follows:

1. The phenotypic and genotypic ratio of the F1 generation is d. 100% purple; 100% Pp.

2. The phenotypic and genotypic ratio of the progeny of this cross, respectively is a. 50% purple and 50% white; 25% PP, 50% Pp, and 25% pp.

3. A purple pea plant of unknown genotype was crossed with a white pea plant. Assume that purple is dominant to white. If 100% of the progeny is phenotypically purple, then what is the genotype of the unknown purple parent? What special type of cross is this that helps identify an unknown dominant genotype? The unknown genotype of the purple parent is Pp. The type of cross is a test cross.

4. A purple pea plant of unknown genotype was crossed with a white pea plant. Assume that purple is dominant to white. Of 1000 offspring, 510 were purple, and 490 were white; the genotype of the unknown purple parent must be Pp.

5. Yellow pea color is dominant to green pea color. Round seed shape is dominant to wrinkled seed shape. A doubly heterozygous plant is self-fertilized. What phenotypic ratio would be observed in the progeny? The correct option is b. 9:3:3:1.

6. What is the genotype of a homozygous recessive individual? The correct option is c. ee.

7. Red-green color blindness is an X-linked recessive trait. Jane, whose father was colorblind but is normal herself, has a child with a normal man. What is the probability that the child will be colorblind? The correct option is b. 1/4.

8. Red-green color blindness is an X-linked recessive trait. Jane, whose father was colorblind but is normal herself, has a child with a normal man. What is the probability that a son will be color-blind? The correct option is d. 2/3.

9. Flower color in snapdragons is an example of incomplete dominance. A pure-breeding red plant is crossed with a pure-breeding white plant. The offspring were found to be pink. If two pink flowers are crossed, what phenotypic ratio would we expect? The correct option is d. 1 Red: 1 Pink.

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Which of the following about the phycosphere is incorrect? O Photosynthetic bacteria use flagella to swim toward the phycosphere to obtain organic carbon nutrients O Chemotactic bacteria use flagella to swim toward the phycosphere to obtain organic carbon nutrients O Chemotactic bacteria detect and swim toward the microenvironment around the phycosphere via chemoreceptors of the chemosensing system O in the increasing concentration of organic carbon in the phycosphere, tumbling frequency is reduced and runs are longer

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The given options are all correct statements about the phycosphere, the microenvironment surrounding algal cells.

Photosynthetic bacteria are known to use flagella as a means to swim toward the phycosphere, where they can obtain organic carbon nutrients released by the algae. Similarly, chemotactic bacteria utilize their flagella and chemosensing systems to detect and navigate toward the microenvironment around the phycosphere, attracted by the presence of organic carbon.

Within the phycosphere, there is an increasing concentration of organic carbon due to the release of nutrients by the algae. This high concentration of organic carbon has an impact on bacterial behavior. The tumbling frequency of bacteria is reduced, and they engage in longer "runs" as they move within the phycosphere, enabling them to better explore and exploit the nutrient-rich environment.

The phycosphere plays a crucial role in the intricate relationships between algae and bacteria in aquatic ecosystems. These interactions have significant implications for nutrient cycling, algal growth, and overall ecosystem functioning. The accurate understanding of bacterial behavior and dynamics in the phycosphere is essential for studying and managing aquatic environments effectively.

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Bacteria use a number of ways to control gene expression. The enzymes required for the biosynthesis of the amino acid tryptophan are synthesized only if tryptophan is not available in the growth medium, ie trp operon is expressed only in the absence of tryptophan. The trp operon of E. coli is not only controlled through a regulatory protein but also by transcription attenuation.
Answer all questions-
1. What is gene expression?
2. List different methods that bacteria can use to regulate gene expression at the transcription step.
3. Describe the regulation of trp operon by attenuating transcription in the presence of tryptophan.
4. Describe the regulation of trp operon by attenuating transcription in the absence of tryptophan.

Answers

The regulation of the trp operon by transcription attenuation is a complex process and involves the interplay of regulatory proteins, RNA structures, and metabolite binding.

1. Gene expression refers to the process by which information encoded in a gene is used to synthesize a functional gene product, such as a protein or RNA molecule. It involves multiple steps, including transcription (the synthesis of RNA from DNA) and translation (the synthesis of protein from RNA).

2. Bacteria can use several methods to regulate gene expression at the transcription step. These include:

Promoter regulation: Bacteria can control gene expression by altering the activity of the promoter region, which is responsible for initiating transcription. This can be achieved through the binding of regulatory proteins that either enhance (activators) or inhibit (repressors) transcription.Transcription factors: Bacteria can utilize specific proteins called transcription factors that bind to DNA and regulate the transcription of specific genes. These transcription factors can either activate or repress gene expression.DNA methylation: Methylation of DNA bases can affect gene expression by either promoting or inhibiting transcription. Methylation patterns can be heritable and can influence gene expression patterns in bacteria.Transcriptional attenuation: This is a regulatory mechanism where the transcription process is prematurely terminated before the full gene product is synthesized. It typically involves the formation of specific RNA structures that can either allow or hinder the progression of RNA polymerase during transcription.

3. In the presence of tryptophan, the trp operon is regulated by transcription attenuation. The trp operon contains genes involved in tryptophan biosynthesis. When tryptophan is abundant, it acts as a co-repressor, binding to a regulatory protein called the trp repressor. The trp repressor-trp complex then binds to a specific region of the trp mRNA, called the attenuator region.

4. In the absence of tryptophan, the trp operon is regulated by attenuating transcription in a different manner. When tryptophan levels are low, the trp repressor does not bind to tryptophan, and instead, a different RNA structure forms in the attenuator region of the trp mRNA. This structure allows RNA polymerase to continue transcribing the trp operon, resulting in the synthesis of enzymes involved in tryptophan biosynthesis.

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Which of the following is a FALSE statement? The contractile ring is composed of actin filaments and myosin filaments. Microtubule-dependent motor proteins and microtubule polymerization and depolymerization are mainly responsible for the organized movements of chromosomes during mitosis. Sister chromatids are held together by cohesins from the time they arise by DNA replication until the time they separate at anaphase. Condensins are required to make the chromosomes more compact and thus to prevent tangling between different chromosomes Each centromere contains a pair of centrioles and hundreds of gamma-tubulin rings that nucleate the growth of microtubules.

Answers

The false statement among the following options is  "Each centromere contains a pair of centrioles and hundreds of gamma-tubulin rings that nucleate the growth of microtubules."

What are centromeres? Centromeres are the region of the chromosomes that helps to separate the replicated chromosomes between two cells during cell division. They provide a site for the kinetochore complex to attach to spindle fibers during cell division. The centromere is considered to be the most critical part of the chromosome during cell division.

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Conversion of 1 mole of acetyl-CoA to 2 mole of CO2 and 1 mole of CoASH in the citric acid cycle also results in the net production of: 1 mole of FADH2 1 mole of oxaloacetate 1 mole of citrate 1 mole of NADH 4 mole of ATP

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The net production of 1 mole of FADH2, 1 mole of NADH, 1 mole of GTP, and 4 mole of ATP results from the conversion of 1 mole of acetyl-CoA to 2 mole of CO2 and 1 mole of CoASH in the citric acid cycle. GTP is later converted to ATP by the enzyme nucleoside diphosphate kinase.

Conversion of 1 mole of acetyl-CoA to 2 mole of CO2 and 1 mole of CoASH in the citric acid cycle also results in the net production of 1 mole of FADH2, 1 mole of NADH, 1 mole of GTP and 4 mole of ATP.The citric acid cycle, also known as the Krebs cycle or the tricarboxylic acid cycle, is a crucial metabolic pathway that occurs in the mitochondrial matrix of eukaryotic cells and in the cytosol of prokaryotic cells. In the citric acid cycle, acetyl-CoA is oxidized, producing 2 CO2 molecules, 1 ATP molecule, 3 NADH molecules, and 1 FADH2 molecule. These molecules are then used in the electron transport chain to generate ATP by oxidative phosphorylation, which is the primary source of ATP in eukaryotic cells.The net production of 1 mole of FADH2, 1 mole of NADH, 1 mole of GTP, and 4 mole of ATP results from the conversion of 1 mole of acetyl-CoA to 2 mole of CO2 and 1 mole of CoASH in the citric acid cycle. GTP is later converted to ATP by the enzyme nucleoside diphosphate kinase.

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Concept Check (Shoulder and elbow movement exercise) 1. The muscle primarily responsible for a muscle movement is the synergist. True False 2. The muscle that assists a prime mover is called an agonis

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It is FALSE that the muscle primarily responsible for a muscle movement is the synergist.

The muscle primarily responsible for a muscle movement is the agonist or prime mover. The agonist is the muscle that contracts and generates the force required for a specific movement. It is the primary muscle responsible for producing a desired action at a joint. The synergist muscles, on the other hand, assist the agonist in performing the movement by stabilizing the joint or providing additional support. Synergist muscles may also help fine-tune the movement or contribute to the overall efficiency of the action. Therefore, while the synergist muscles play a supportive role, the agonist muscle is the primary muscle responsible for initiating and executing a specific movement.

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What are the differences between the T and R state of haemoglobin? Describe the physiological conditions under which each of these states of haemoglobin would be favoured in the body. 7 A- B I !!! III

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The T state is the deoxyhaemoglobin form, whereas the R state is the oxyhaemoglobin form. Haemoglobin (Hb) is an oxygen-carrying protein found in red blood cells. Hb binds to oxygen (O2) to form oxyhaemoglobin. When O2 is released, deoxyhaemoglobin is formed. Hb exists in two forms, T and R states.

The T state of haemoglobin is the deoxygenated or tense state. It is stabilized by ionic bonds and hydrogen bonds that maintain the quaternary structure of the protein. In the T state, the heme groups are positioned differently, making it more difficult for oxygen to bind to haemoglobin. Hence, it has low oxygen affinity.What is the R state of haemoglobin?The R state of haemoglobin is the oxygenated or relaxed state. When oxygen binds to haemoglobin, the iron ion within the heme group undergoes a conformational change.

It causes a rotational change in the quaternary structure of haemoglobin, resulting in a looser structure. This makes it easier for subsequent O2 molecules to bind to the remaining heme groups of Hb. Therefore, it has high oxygen affinity. The T state is favored in tissues with low O2 concentrations, such as muscle tissues during exercise, where O2 is released from Hb to provide energy through aerobic respiration. At high altitude, where O2 concentration is low, the T state of Hb is favored in the lungs to promote O2 uptake. Acidic conditions, high temperature, and high 2,3-bisphosphoglycerate (BPG) concentrations also favor the T state.The R state is favored in areas of high O2 concentrations, such as the lungs.

It occurs at physiological pH and low 2,3-BPG concentration. This promotes oxygen binding to haemoglobin for transportation to tissues that require oxygen. The R state of haemoglobin is more stable and is a result of stronger bonds between the subunits of haemoglobin.

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The following are red blood cells in solution. Indicate the movement of the water for each and label the solutions as hypertonic, hypotonic or isotonic. 10% water 90% solute is_____
60% water 40% solute is____
70% water 30% solute is____
10. Cells shrink when placed in which solution? Cells swell and can burst when placed in which solution? Cells remain the same size when placed in which solution?

Answers

Red blood cells play an important role in human physiology by transporting oxygen from the lungs to the body's tissues and removing carbon dioxide. The movement of water in red blood cells (RBCs) can be hypertonic, hypotonic, or isotonic depending on the solute concentration inside and outside the cell.

The 10%, 60%, and 70% water and solute solutions are hypertonic, hypotonic, and isotonic, respectively. The solution that causes the cell to shrink is a hypertonic solution. When placed in a hypotonic solution, cells swell and can even burst. When placed in an isotonic solution, cells remain the same size.

The movement of water in red blood cells (RBCs) depends on the tonicity of the solution in which they are placed. The tonicity of a solution is determined by its concentration of solutes. If the solute concentration is higher outside the cell than inside, the solution is hypertonic.

When the solute concentration is lower outside the cell than inside, the solution is hypotonic. In contrast, an isotonic solution has an equal solute concentration inside and outside the cell.

10% water 90% solute is hypertonic. In this solution, the concentration of solutes outside the cell is higher than inside, causing water to move out of the cell. This movement causes the RBC to shrink or crenate.

60% water 40% solute is hypotonic. In this solution, the concentration of solutes outside the cell is lower than inside, causing water to move into the cell. This movement causes the RBC to swell or lyse.

70% water 30% solute is isotonic. In this solution, the concentration of solutes is equal inside and outside the cell. As a result, there is no net movement of water, and the RBC remains the same size.

Cells shrink when placed in a hypertonic solution. This is because the concentration of solutes is higher outside the cell than inside, causing water to move out of the cell. As a result, the RBC loses water and shrinks. In contrast, cells swell and can burst when placed in a hypotonic solution.

This is because the concentration of solutes is lower outside the cell than inside, causing water to move into the cell. As a result, the RBC gains water and swells, which may cause the cell to burst. Finally, cells remain the same size when placed in an isotonic solution because the concentration of solutes is equal inside and outside the cell.

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E Which of the following cells is responsible for producing antibodies? A B cells B T cells Eosinophils Neutrophils

Answers

B cells are responsible for producing antibodies. Therefore option A) B cells is correct.

B cellsv- B cells, also known as B lymphocytes, are a type of white blood cell that is responsible for producing antibodies. B cells can identify foreign substances and then generate antibodies that recognize those substances and neutralize them.

The immune system can produce millions of different B cells, each with its own unique antigen receptor on its surface. When a B cell encounters its corresponding antigen, it is activated and begins to multiply.

The offspring of these activated B cells are referred to as plasma cells, which are capable of producing a massive amount of antibodies.

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Question 22 0/3 pts Which of the following is not true about the anabolic pathways of all amino acids? The starting material for anabolism are intermediates in energy metabolism pathways. Anabolism requires the use of acetyl-CoA. The anabolism involves an aminotransferase. All of the above are true for the anabolism of all amino acids. None of the above is true for the anabolism of all amino acids. rect Question 23 0/3 pts Which of the following amino acids has the longest anabolic pathway? Aspartate Alanine Glutamate Phenylalanine The anabolic pathways of all amino acids are the same length. rect Question 24 0/3 pts Which of the following is true about the anabolism of heme? It has an amino acid as a precursor. a Heme is essential to human beings but can be made in plants. The source of the biggest number of atoms is the same as the source of the biggest number of atoms in the purine nucleotides. It is made from cholesterol. Both A and C are true

Answers

None of the above is true for the anabolism of all amino acids. The statement that is not true about the anabolic pathways of all amino acids is "All of the above are true for the anabolism of all amino acids." Anabolism of all amino acids does not always involve the same reactions, so the anabolic pathways are not the same for all amino acids.

Phenylalanine is the amino acid with the longest anabolic pathway. It has the longest anabolic pathway because it is an essential amino acid, meaning that it cannot be synthesized by the human body. It must be ingested through the diet, and it must be converted to tyrosine for use by the body.

Both A and C are true. The two true statements about the anabolism of heme are "It has an amino acid as a precursor" and "The source of the biggest number of atoms is the same as the source of the biggest number of atoms in the purine nucleotides." Heme synthesis begins with glycine, an amino acid. The source of the biggest number of atoms in heme is also the source of the biggest number of atoms in the purine nucleotides, which are synthesized from the molecule IMP (inosine monophosphate).

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Question 35 The enzyme responsible for digesting sucrose is known as sucrase which breaks sucrose down into O glucose and galactose O glucose and glucose O glucose and fructose O fructose and fructose

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The enzyme responsible for digesting sucrose is known as sucrase, which breaks sucrose down into glucose and fructose.

Sucrase is a type of enzyme called a carbohydrase that plays a crucial role in the digestion of sucrose, a disaccharide commonly found in many foods. When we consume sucrose, sucrase is produced in the small intestine to facilitate its breakdown. The enzyme sucrase acts on the glycosidic bond present in sucrose, which connects glucose and fructose molecules. By cleaving this bond, sucrase effectively splits sucrose into its constituent monosaccharides: glucose and fructose.

Once sucrose is broken down into glucose and fructose, these individual sugars can be readily absorbed by the small intestine and enter the bloodstream. From there, they are transported to various cells throughout the body to provide energy for cellular processes. The breakdown of sucrose by sucrase is an essential step in the digestion and absorption of carbohydrates, allowing our bodies to utilize the energy stored in this common dietary sugar.

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Use the ions and match them to the appropriate scenario. What ion is important in muscle contraction cycle? [Choose his ion passes through the resting neuron's cell membrane the easiest. [Choose [Choo

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The ion important in the muscle contraction cycle is calcium (Ca^{2+}). The ion that passes through the resting neuron's cell membrane the easiest is potassium ([tex]K^{+}[/tex]).

Muscle Contraction Cycle: Calcium ([tex]Ca^{2+}[/tex]) is a crucial ion in the muscle contraction cycle. During muscle contraction, calcium ions are released from the sarcoplasmic reticulum in response to a neural signal. The binding of calcium to the protein troponin triggers a series of events that allow actin and myosin to interact, leading to muscle contraction.

Resting Neuron's Cell Membrane: The ion that passes through the resting neuron's cell membrane the easiest is potassium (K^{+}). Neurons have specialized channels, called potassium channels, that allow potassium ions to move in and out of the cell. These channels are responsible for maintaining the resting membrane potential of the neuron. At rest, the neuron's membrane is more permeable to potassium ions, and they tend to move out of the cell, leading to a negative charge inside the neuron.

The movement of potassium ions contributes to the generation and propagation of action potentials in neurons. When an action potential is initiated, there is a temporary increase in the permeability of the cell membrane to sodium ions ([tex]Na^{+}[/tex]), allowing them to enter the cell and depolarize the membrane. However, during the resting state, potassium ions play a key role in maintaining the resting membrane potential.

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Malonyl-CoA inhibits the rate of fatty acid respiration by ____________________________
a. inhibiting the regeneration of NAD+ by the electron transport chain
b. allosteric inhibition of the enzyme that catalyzes acyl-carnitine formation
c. allosteric inhibition of the reaction that activates fatty acids
Based on the overall reaction below, consumption of palmitoyl-CoA in matrix of the mitochondria causes ________________________.
a. a decrease in palmitoyl-CoA concentration in the cytosol
b. an increase in the rate of oxidative phosphorylation
c. a decrease in the rate of palmitic acid coming from the blood into the cell

Answers

Malonyl-CoA inhibits the rate of fatty acid respiration by allosteric inhibition of the enzyme that catalyzes acyl-carnitine formation.

Palmitoyl-CoA consumption in the matrix of the mitochondria causes a decrease in palmitoyl-CoA concentration in the cytosol.

The rate of fatty acid respiration in the mitochondria is controlled by several mechanisms including the availability of free fatty acids, the transport of fatty acids into the mitochondria, and the enzymatic process that oxidizes fatty acids, producing energy in the form of ATP.

Malonyl-CoA is a molecule that inhibits the rate of fatty acid respiration by allosteric inhibition of the enzyme that catalyzes acyl-carnitine formation. This molecule serves as a metabolic regulator that can prevent excessive fatty acid oxidation.

It is synthesized by the enzyme acetyl-CoA carboxylase (ACC) in response to high levels of glucose and insulin.

The consumption of palmitoyl-CoA in the matrix of the mitochondria causes a decrease in palmitoyl-CoA concentration in the cytosol.

This concentration gradient serves as a driving force for the uptake of more fatty acids from the bloodstream. The rate of oxidative phosphorylation is also affected by the availability of fatty acids for oxidation. The more fatty acids that are available for oxidation, the higher the rate of oxidative phosphorylation.

Therefore, the consumption of palmitoyl-CoA in the matrix of the mitochondria would increase the rate of oxidative phosphorylation.

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When plant cells divide, they synthesize a new wall of the cell plate to physically separate two daughter cells.
a) How do plant cells synthesize the cell plate?
b) What molecules are deposited into the cell plate?

Answers

a) Synthesis of the cell plate in plant cells takes place by the vesicles containing cell wall material. These vesicles come together, aligning and fusing to form a disc-shaped cell plate between the two daughter cells.

The cell plate acts as the precursor for the cell wall and it comprises of the same material as that of the cell wall. This process is termed cytokinesis and it occurs in the later stages of mitosis.

b) The cell plate consists of pectin and cellulose. Pectin is a type of polysaccharide that contributes to the wall's gel-like consistency, while cellulose is a component of the cell wall.

This is deposited by the Golgi apparatus into the cell plate during cytokinesis. It forms the primary wall that surrounds the cell, which then gets thickened and becomes the secondary wall in some cells.

The cell wall is essential for maintaining the shape and size of the cell, which in turn is crucial for the normal functioning of the cell and overall plant growth.

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Structures of Sensory Perception 1. Optic nerve 2. Chemoreceptor 3. Photoreceptor 4. Occipital lobe 5. Temporal lobe 6. Auditory nerve After light enters the eye, the structures of sensory perception listed above that are stimulated, in order, are and 3, 1, and 5. O 3, 1, and 4. O2, 6, and 5. 1, 3, and 5.

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The structures of sensory perception play a crucial role in allowing organisms to interact with their environment. The photoreceptor, optic nerve, and temporal lobe are stimulated in order when light enters the eye, and chemoreceptors and the auditory nerve are responsible for detecting chemical and sound stimuli, respectively.

Sensory perception is an important aspect of living organisms that allows them to interact with their surroundings.

The structures of sensory perception that contribute to sensory perception include the optic nerve, chemoreceptors, photoreceptors, occipital lobe, temporal lobe, and auditory nerve.

When light enters the eye, the structures of sensory perception that are stimulated in order are photoreceptor, optic nerve, and temporal lobe.

The photoreceptors located in the retina convert light into electrical signals, which then travel through the optic nerve to the visual cortex in the temporal lobe of the brain.

The temporal lobe is responsible for processing visual information and interpreting it as images.

The occipital lobe is also involved in visual processing, but it receives information from the visual cortex in the temporal lobe.

Chemoreceptors are responsible for detecting chemical stimuli, such as odors and tastes.

They are found in the nose and tongue, and the information they gather is sent to the brain for processing.

The auditory nerve is responsible for transmitting sound signals from the ear to the brain. The sound waves are converted into electrical signals in the cochlea of the inner ear, which then travel through the auditory nerve to the auditory cortex in the temporal lobe.

In conclusion, the structures of sensory perception play a crucial role in allowing organisms to interact with their environment.

The photoreceptor, optic nerve, and temporal lobe are stimulated in order when light enters the eye, and chemoreceptors and the auditory nerve are responsible for detecting chemical and sound stimuli, respectively.

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Summarize emphysema, including causes, treatment, frequency, etc.
Fully explain the disease.

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Emphysema is a chronic lung disease characterized by the destruction of the air sacs (alveoli) in the lungs, leading to breathing difficulties. It is primarily caused by long-term exposure to irritants i.e. cigarette smoke.

Emphysema is a type of chronic obstructive pulmonary disease (COPD) that primarily affects the alveoli, which are responsible for gas exchange in the lungs. Prolonged exposure to irritants, particularly cigarette smoke, leads to inflammation and damage to the walls of the alveoli. This damage causes the air sacs to lose their elasticity, resulting in their permanent enlargement and reduced ability to effectively exchange oxygen and carbon dioxide.

The most common cause of emphysema is smoking, although long-term exposure to other irritants like air pollution or workplace chemicals can also contribute to the development of the disease. Genetic factors, such as alpha-1 antitrypsin deficiency, can increase the risk of developing emphysema in some individuals.

Symptoms of emphysema include shortness of breath, chronic cough, wheezing, fatigue, and chest tightness. As the disease progresses, these symptoms worsen and can significantly impact a person's daily activities.

Treatment for emphysema aims to manage symptoms, slow disease progression, and improve overall lung function. Lifestyle changes such as smoking cessation, avoiding exposure to irritants, and regular exercise are crucial. Medications like bronchodilators and inhaled corticosteroids help to open the airways and reduce inflammation. In severe cases, supplemental oxygen therapy may be required.

Emphysema is a prevalent condition, particularly among smokers, and its frequency has been increasing worldwide. It is a chronic and progressive disease that can significantly impact a person's quality of life and overall health. Early diagnosis, prompt treatment, and lifestyle modifications are essential in managing the symptoms and slowing the progression of emphysema.

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What is the result of using a Anti-Body with a Antigen?

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When an antibody and an antigen interact, a specific biochemical reaction occurs. This type of reaction occurs when the antibody binds to the antigen, forming an antigen-antibody complex. This specific biochemical reaction occurs as a result of the complement activation cascade.

The complement system is a part of the immune system, which is responsible for destroying foreign substances that enter the body. In this case, the complement system is activated when the antigen-antibody complex is formed, leading to the destruction of the foreign substance. Antibodies are specific proteins that recognize and bind to specific antigens. Antigens are molecules that stimulate an immune response, typically by the production of antibodies. Antibodies can be produced naturally by the immune system, or they can be generated artificially in the laboratory. The use of antibodies as a tool for detection and treatment of disease has revolutionized medicine over the past century. For example, antibodies are used in immunoassays to detect the presence of specific proteins in blood or other fluids.

They are also used as therapeutic agents to treat a variety of diseases, including cancer, autoimmune disorders, and infectious diseases.

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Define and be able to identify the following terms as they relate to the hair: a. Shaft b. Root C. Matrix d. Hair follicle e. Arrector pili muscle Define and be able to identify the following terms as

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The arrector pili muscle is responsible for causing the hair to stand upright when it contracts.As it relates to hair, the following terms can be defined and identified:

a. ShaftThe shaft of the hair is the portion of the hair that is visible on the surface of the skin. The shaft is the part of the hair that we can see, and it is made up of dead skin cells that have become keratinized, or hardened.

b. RootThe root of the hair is the part of the hair that is located beneath the skin's surface. The root is the part of the hair that is responsible for producing the hair shaft.

c. MatrixThe matrix is a layer of cells located at the base of the hair follicle. The matrix is responsible for producing new hair cells, which will eventually become part of the hair shaft.

d. Hair follicleThe hair follicle is a structure located beneath the skin's surface that produces hair. The hair follicle is responsible for producing and maintaining the hair shaft.e. Arrector pili muscleThe arrector pili muscle is a small muscle located at the base of each hair follicle.

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gigas (gig, fly TSC2) mutant clones the corresponding WT twin spots were generated during Drosophila eye development, determine whether the following statements are true or false:
A. gig mutant clones will be larger than twin spots with larger cells
B. gig mutant clones will be larger than twin spots with more cells
C. gig mutant clones will be smaller than twin spots with smaller cells

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The true or false of the following statements for gigas (gig, fly TSC2) mutant clones and their corresponding WT twin spots during Drosophila eye development are: A. gig mutant clones will be larger than twin spots with larger cells - False. B. gig mutant clones will be larger than twin spots with more cells - True. C. gig mutant clones will be smaller than twin spots with smaller cells - False.

The true or false of the following statements for gigas (gig, fly TSC2) mutant clones and their corresponding WT twin spots during Drosophila eye development are:

A. gig mutant clones will be larger than twin spots with larger cells - False.

B. gig mutant clones will be larger than twin spots with more cells - True

C. gig mutant clones will be smaller than twin spots with smaller cells - False.

In Drosophila melanogaster eye, it has been shown that Tuberous Sclerosis Complex (TSC) regulates cell size and number through the protein kinase complex Target of Rapamycin Complex 1 (TORC1) and the transcription factor Myc.

A reduction in TSC function results in larger cells with more nucleoli, a phenotype that is commonly used to identify cells with elevated TORC1 signaling. When determining if the statements A, B, and C are true or false, the following explanation can be used:

A. False. Gig mutant clones will not be larger than twin spots with larger cells because, in this scenario, cell size is not altered.

B. True. Gig mutant clones will be larger than twin spots with more cells because the function of the gig is associated with cell number, as described in the explanation.

C. False. Gig mutant clones will not be smaller than twin spots with smaller cells because the function of the gig is not related to cell size.

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Which cells are capable of presenting an antigen to another cell?
a. Describe the process an APC goes through in order to present and antigen to another cell.
b. Include the role of cytokines (interleukins)

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Antigen-presenting cells (APCs) are capable of presenting antigens to other cells. The process of antigen presentation involves the uptake, processing, and presentation of antigens on major histocompatibility complex (MHC) molecules. Cytokines, such as interleukins, play a crucial role in regulating the immune response and activating APCs.

Antigen-presenting cells (APCs) include dendritic cells, macrophages, and B cells. These cells play a critical role in the immune system by capturing and presenting antigens to other immune cells, such as T cells.

The process of antigen presentation starts with the uptake of antigens by APCs. This can occur through phagocytosis or endocytosis of pathogens, cellular debris, or foreign substances. Once inside the APC, the antigens are processed and broken down into smaller peptide fragments.

The processed antigens are then presented on the surface of APCs using specialized proteins called major histocompatibility complex (MHC) molecules. MHC class II molecules present antigens derived from extracellular sources, while MHC class I molecules present antigens from intracellular sources.

In the presence of an infection or immune response, cytokines, including interleukins, are released. Cytokines play a crucial role in regulating the immune response and activating APCs. Interleukins, in particular, can enhance the expression of MHC molecules on APCs, promote antigen processing, and facilitate T-cell activation.

In summary, antigen-presenting cells (APCs) are capable of presenting antigens to other cells. The process involves the uptake, processing, and presentation of antigens on MHC molecules. Cytokines, such as interleukins, play a role in regulating the immune response and activating APCs by enhancing antigen presentation and promoting T-cell activation.

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Which of the following issues would not be included in a food safety management system?
The number of pieces of egg shell in powdered milk. The heating instructions on the package say "do not microwave this food" but the consumer microwaves and then eats the food. The concentration of N2(g) in a modified atmosphere package. The receiving temperature of a fluid milk product arriving at an ice cream manufacturer.

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This issue would be included in a food safety management system.The heating instructions on the package say "do not microwave this food" but the consumer microwaves and then eats the food is not a food safety issue.

A food safety management system (FSMS) is a systematic method for identifying and preventing hazards in food production and distribution. It is designed to ensure that food products are safe for human consumption.

The following issue, "The heating instructions on the package say "do not microwave this food" but the consumer microwaves and then eats the food" would not be included in a food safety management system.

Below are the reasons why the other options would be included in a food safety management system and the fourth option would not be included in an FSMS:

1. The number of pieces of eggshell in powdered milk: Eggshell pieces in powdered milk may cause physical contamination of the product.

As a result, this issue would be included in a food safety management system.

2. The concentration of N2(g) in a modified atmosphere package: The atmosphere in modified atmosphere packages is altered to extend the shelf life of food products. The concentration of N2(g) is closely monitored to ensure that it meets specific requirements.

As a result, this issue would be included in a food safety management system.

3. The receiving temperature of a fluid milk product arriving at an ice cream manufacturer: The temperature at which milk is stored during transportation has a significant impact on its shelf life.

As a result, this issue would be included in a food safety management system.

The heating instructions on the package say "do not microwave this food" but the consumer microwaves and then eats the food is not a food safety issue.

As a result, this issue would not be included in a food safety management system. Hence, this is the answer to the question.

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1. Describe a scenario in which it would be appropriate to use azithromycin to treat AOM.
2. Review the literature for evidence supporting antibiotic prophylaxis therapy in children with frequent ear infections.

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A scenario in which it would be appropriate to use azithromycin to treat AOM is with a child has been diagnosed with AOM by a doctor.

There is some evidence to support the use of antibiotic prophylaxis therapy in children with frequent ear infections.

When to treat AOM with azithromycin ?

Azithromycin can be given as a single dose or as a course of multiple doses. The single-dose regimen is more convenient, but it may not be as effective as the multi-dose regimen.

Scenarios where one can use azithromycin to treat AOM:

The child is younger than 6 years old.The child has had at least three episodes of AOM in the past 6 months.The child has not had a recent viral infection.

One study found that antibiotic prophylaxis was effective in reducing the number of ear infections in children who had had at least four episodes of AOM in the past year. However, the study also found that antibiotic prophylaxis was associated with an increased risk of antibiotic resistance.

Another study found that antibiotic prophylaxis was not effective in reducing the number of ear infections in children who had had at least three episodes of AOM in the past year.

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Suppose you have a plentiful supply of oak leaves are about 49% carbon by weight. Recall our autotutorial "Soil Ecology and Organic Matter," where we calculated N surpluses (potential N mineralization) and N deficits (potential N immobilization) based on the C:N ratios of materials that one might incorporate into soils. We assumed that just 35% of C is assimilated into new tissue because 65% of C is lost as respiratory CO2, and that soil microorganisms assimilate C and N in a ratio of 10:1. Using these assumptions, please estimate the potential N mineralization or immobilization when 97 pounds of these oak leaves with C:N = 62:1 are incorporated into soil. If this number (in pounds of N) is a positive number (mineralization), then just write the number with no positive-sign. However, if this number (in pounds of N) is negative (immobilization), then please be sure to include the negative-sign! Your Answer:

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Oak leaves are approximately 49 percent carbon by weight. We will estimate the potential N mineralization or immobilization when 97 pounds of these oak leaves with C:

where we calculated N surpluses (potential N mineralization) and N deficits (potential N immobilization) based on the C.

N = 62:1

are incorporated into the soil using the assumptions from the auto tutorial.

"Soil Ecology and Organic Matter,".

N ratios of materials that one might incorporate into soils.

We know that,

C:

N ratio for oak leaves is 62:

As per the given, just 35% of C is assimilated into new tissue because 65% of C is lost as respiratory CO2.

and soil microorganisms assimilate C and N in a ratio of 10:1.

Assuming a starting value of 97 l bs of oak leaves,

the carbon contained in them can be calculated as follows:97.

the potential N mineralization or immobilization can be calculated as follows:

47.53 l.

bs carbon * 0.35 = 16.64 l.

bs carbon in new tissue.

47.53 l.

bs carbon * 0.65 = 30.89 l.

bs respiratory CO2For 16.64 l.

bs of new tissue,

we can assume that the microorganisms will assimilate 1.664 l bs of N.

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J.A. Moore investigated the inheritance of spotting patterns in leopard frog (J.A. Moore, 1943. Journal of Heredity 34:3-7). The pipiens phenotype had the normal spots that give leopard frogs their name. In contrast, the burnsi phenotype lacked spots on its back. Moore carried out the following crossed, producing the progeny indicated.
Parent phenotypes Progeny phenotypes Cross #1: bumsi x burnsi 35 bumsi, 10 pipiens Cross 2: burnsi x pipiens 23 burnsi, 33 pipiens Cross N3: burnsi x pipiens 196 burnsi, 210 pipiens a. On the basis of these results, which allele is dominant-burnsi or pipiens? Pipiens = __________ Bumsi_________ b. Give the most likely genotypes of the parent in each cross Parent phenotypes Write Parent Genotypes below: Cross #1: burnsi x burnsi __________x_________
Cross #2: burnsi x pipiens __________x_________
Cross #3: bumsi x pipiens __________x_________
Chi-Square for cross #1: Value____ P value _____
Chi-Square for cross #2: Value____ P value ______
Chi-Square for cross #3 Value____ P value ______
b. What conclusion can you make from the results of the chi-square test? c. Suggest an explanation for the results.

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J.A. Moore investigated the inheritance of spotting patterns in leopard frog (J.A. Moore, 1943. Journal of Heredity 34:3-7).

The pipiens phenotype had the normal spots that give leopard frogs their name. In contrast, the burnsi phenotype lacked spots on its back. Moore carried out the following crossed, producing the progeny indicated .a. On the basis of these results, the allele that is dominant is pipiens. Pipiens = 33+210= 243Bumsi = 23+196= 219b. The most likely genotypes of the parent in each cross: Parent phenotypes Parent Genotypes below: Cross #1: burnsi x burnsibb x bb Cross #2: burnsi x pipiens bb x Bb Cross #3: bumsi x pipiens Bb x Bbc.

The Chi-square values for cross #1, #2, and #3 are given below. Chi-Square for cross #1: Value 0.08 P value 0.78Chi-Square for cross #2: Value 1.07 P value 0.30Chi-Square for cross #3 Value 0.06 P value 0.80The null hypothesis is that there is no significant difference between the observed and expected data, while the alternative hypothesis is that there is a significant difference between the observed and expected data.

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Which of the following is NOT a situation showing females have mate choice? O A. Females mate with a male that provides a nutritional benefit B. Females mate with a male that signals his resistance to disease C. Females mate with a male that is preferred by other females D. Females mate with a male that wins the fight to monopolize her group

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The situation showing females have mate choice is females' mate with a male that wins the fight to monopolize her group. It is NOT a situation that shows females have mate choice.

Explanation: Mate choice is an evolutionary process in which the choice of an individual female for a particular male is based on certain characteristics or traits of that male.

In this case, the male is not chosen by the female based on any specific trait or characteristic, but rather the male has asserted dominance over the group and monopolized the female. Therefore, this is not a situation of mate choice but rather a situation of male dominance.

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All of the following are criteria of chromophiles of pars distalis, except: Select one: a. They form 50% of the cells of pars distalis b. They are formed by acidophils and basophils c. They have few g

Answers

a.They form 50% of cell of pars distalis.

The main answer is that chromophiles of pars distalis do not necessarily form 50% of the cells. The percentage of chromophiles can vary, and it is not a definitive criterion for their classification.

Chromophiles are a type of endocrine cells found in the anterior pituitary gland, specifically in the pars distalis region. They play a crucial role in producing and releasing hormones that regulate various physiological processes in the body.

The classification of chromophiles is based on the staining properties of their secretory granules, which can be either acidic (acidophils) or basic (basophils).

The criteria for identifying chromophiles include their staining characteristics, the presence of secretory granules, and their hormone production. Acidophils secrete hormones such as growth hormone and prolactin, while basophils produce hormones such as adrenocorticotropic hormone (ACTH), thyroid-stimulating hormone (TSH), and follicle-stimulating hormone (FSH).

However, the percentage of chromophiles in the pars distalis can vary depending on several factors, including individual variations, hormonal status, and pathological conditions. The proportion of chromophiles can range from less than 50% to more than 50% of the total cells in the pars distalis. Therefore, the statement that they form 50% of the cells is not a definitive criterion for chromophiles and cannot be used to distinguish them.

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Urea synthesis in mammals takes place primarily in tissues of
the:
A.
Brain
B.
Liver
C.
Kidney
D.
Skeletal muscle

Answers

The correct answer is B. Liver. Urea synthesis in mammals primarily occurs in the liver.

The liver plays a crucial role in the metabolism of nitrogenous compounds, including the conversion of ammonia into urea through a series of enzymatic reactions known as the urea cycle. In the urea cycle, ammonia, which is toxic to the body, is combined with carbon dioxide and transformed into urea. This process occurs mainly in hepatocytes, the functional cells of the liver. The liver receives ammonia from various sources, including the breakdown of amino acids from dietary proteins and the degradation of cellular proteins.

Once synthesized in the liver, urea is released into the bloodstream and transported to the kidneys for excretion in urine. The kidneys are responsible for filtering the blood, maintaining fluid balance, and excreting waste products, including urea.

While the brain, kidney, and skeletal muscle play essential roles in various metabolic processes, including nitrogen metabolism, they do not serve as the primary sites for urea synthesis. Instead, they have different functions related to the regulation of water and electrolyte balance, detoxification, and neurotransmitter synthesis.

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