The following is common to both factor-dependent and factor-independent transcription termination is both types of termination occur following a pause by the polymerase
Factor-dependent and factor-independent are the two types of transcription termination. In factor-independent transcription termination, a DNA sequence containing a GC-rich inverted repeat is essential. The sequence can be followed by a stretch of T's, which are complementary to the A's in the transcript. When a polymerase reaches the terminator sequence, the RNA polymerase transcribes the inverted repeat sequence. As a result, the mRNA folds back on itself, forming a hairpin structure. The formation of a hairpin loop causes the RNA polymerase to pause, resulting in termination.
On the other hand, factor-dependent transcription termination is based on a specific termination factor, Rho. Rho is a protein that binds to the mRNA and travels along it. As the RNA polymerase approaches a termination site, Rho binds to the RNA and triggers the termination process. Therefore, the two transcription termination types have different mechanisms. The only common feature of the two transcription termination types is that they occur following a pause by the polymerase. This is what the two transcription termination types have in common.
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What is the average for the following set of measurements?
7.1 g, 9.8 g, 2.3 g, 8.5 g, 7.4 g, 5.7 g
A. 9.8 g
B. 6.8 g
C. 8.2 g
• D. 40.8 g
Answer:
6.8g
Explanation:
All numbers are added together and you divide the total but the amount of numbers given.
All numbers added equals to 40.8
Numbers given equals 6
40.8 divided by 6 equals 6.8
transport of a solute across a membrane where the solute is going up its concentration gradient and using protein carriers driven by the expenditure of chemical energy, is known as
Transport of a solute across a membrane where the solute is going up its concentration gradient and using protein carriers driven by the expenditure of chemical energy is known as active transport.
What is active transport?Active transport is the movement of molecules against the concentration gradient, which means moving from lower to higher concentrations. It involves a direct energy source (ATP) to drive the movement of molecules. The active transport method involves the use of protein pumps to move molecules across the cell membrane. These pumps can help move molecules, including sodium, calcium, and potassium, against the concentration gradient, which allows the cell to regulate what enters and exits. During active transport, the cell must use energy in the form of ATP to transport the molecules.
In summary, the transport of a solute across a membrane, where the solute is going up its concentration gradient and using protein carriers driven by the expenditure of chemical energy, is known as active transport. Active transport requires energy, which is provided by the hydrolysis of ATP. Active transport is necessary because it allows the cell to maintain its internal environment despite the external environment's changes.
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Predict A store owner has a problem with birds building nests on top of the store’s
outdoor sign. To scare the birds away, she places rubber snakes on top of the sign.
Predict how the birds will react to the rubber snakes. Use the terms habituated,
learn, negative effects, positive effects, and stimulus in your answer.
Answer:
The birds may initially be frightened by the rubber snakes due to the sudden presence of a new stimulus. However, if they do not encounter any negative effects, such as being attacked or injured by the snakes, they may quickly habituate to their presence and no longer see them as a threat. This means that the birds may learn that the rubber snakes are not a danger and may continue to build their nests on the sign, ignoring the presence of the snakes. Therefore, the use of rubber snakes may have no positive effects in deterring the birds from building their nests, but rather may be ineffective or even have negative effects if the birds become habituated to them.
Explanation:
This is what I think hope it helps.
The basic building blocks in a human body are?
Explanation:
cells bro easy one mark brain list
Answer: CELLS
Explanation: The basic building block of a body is formed by a cell, a tissue, muscle, nerve, skin, blood etc. but billions of cells make up the human body
During crossing over, when the invading strand uses the invaded DNA as a _____, this automatically results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected _____ ratio.
The correct answer is: During crossing over, when the invading strand uses the invaded DNA as a template, this automatically results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected 1:1 ratio of crossing over.
Explanation:
DNA is replicated through the process of crossing over, which involves the exchange of genetic material between two homologous chromosomes. During the process, one of the homologous chromosomes acts as the invading sequence, while the other acts as the invaded DNA. When the invading strand uses the invaded DNA as a template, it results in an extra copy of the invaded sequence at the expense of the invading sequence, thus explaining the departure from the expected 1:1 ratio of crossing over.
What is crossing over?
Crossing over is a process during meiosis where the chromosome arms of maternal and paternal homologous chromosomes swap DNA sections (recombination) to produce new allelic combinations of traits. The crossing-over process starts with the breakage of two homologous chromosomes, the migration of the broken ends toward each other, and the formation of crosslinks by the formation of single crossovers.
These crosslinks are eventually converted to chiasmata that keep the chromosomal arms connected until metaphase I. During this process, one chromosome might lose genetic material while the other might acquire genetic material. This event results in unique combinations of genes that might not be present in either parent. The frequency of crossovers is affected by the distance between the gene and the centromere. Chromosomes that are nearer to the centromere are less likely to cross over than those that are further away. Explaining the departure from the expected Mendelian ratio.
The ratio of offspring created by a cross that exhibits the dominant and recessive traits that Mendel observed is referred to as the Mendelian ratio. Crossing over might result in new allelic combinations of genes that deviate from the Mendelian ratios. This is because the transmission of genes is no longer controlled by a single gene pair on a chromosome. Chromosome segregation is disturbed in one way or another by crossovers.
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In 1981, a couple found a stray kitten whose unusual ears curled up and back from her head. They decided to breed her with their male cat who is homozygous for the allele for normal ears. The first litter of kittens produced two kittens with normal ears and two kittens with curled ears. Subsequent litters with the same parents showed the same ratio of curled ears to normal ears. When curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears. This new trait was determined to be the result of a new and unique mutation in the ear gene of cats, and cats with this trait were named American curl cats.
In American curl cats, the allele that produces the ear-curling trait is which?
The allele that produces normal ears is which?
Dominant
Recessive
Page 120
In American curl cats, the allele that produces the ear-curling trait is dominant, while the allele that produces normal ears is recessive. This can be determined from the fact that when curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears, indicating that the ear-curling trait is dominant over the normal ear trait.
In American curl cats, the allele that produces the ear-curling trait is dominant. Dominance is a characteristic of an allele that expresses its phenotype in a heterozygote, such that it masks the expression of a recessive allele. When curled-ear offspring were mated with other curled-ear offspring, three-fourths of the kittens had curled ears and one-fourth had normal ears.
The allele that produces normal ears is recessive. Recessive traits are only expressed in a homozygous state, and that are not expressed in a heterozygous state because a dominant allele mask it. The first litter of kittens produced two kittens with normal ears and two kittens with curled ears. The parents were heterozygous, with one carrying the dominant curled allele and the other carrying the recessive normal allele.
In summary, in American curl cats, the allele that produces the ear-curling trait is dominant. The allele that produces normal ears is recessive.
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Subject: Science
1. Approximately how far away would the formation of Earth be if you used the scale from your timeline?
2. Which events helped life develop on Earth? ''Explain''.
Because several meteorites have been dated, the Earth's age has increased from 4.55 0.3 billion years in 1956 to 4.55 0.02 billion years. I) The synthesis of nucleotides and amino acids.
How did life on Earth start to appear?In rocks that are 3.7 billion years old, the oldest known life forms, microbes, have left their imprint. The signals were made up of a specific class of carbon molecules produced by living things.
What process created the Earth?Formation. Over a period of 4.5 billion years, whenever the solar system was still in its current configuration, the second planet from the Sun—Earth—was created when gravity drew spinning gas and dust in. Earth has a solid crust, a high degree of crystallinity, and a central core, just like its sibling terrestrial planets.
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Where are the olfactory filaments found?
Answer:
nasal cavity
Explanation:
Olfactory filaments
The bipolar cell is the first-order sensory neuron located at the olfactory mucosa on the roof of the nasal cavity, immediately inferior to the cribriform plate of the ethmoid bone. This cell is analogous to the sensory cells of spinal nerves, whose cell bodies reside in the dorsal root ganglion.
during the menstrual cycle, what triggers ovulation to occur? question 23 options: a gradual decrease in estrogen levels. inhibin b sharply spikes. a surge in progesterone occurs. activin is released.
Ovulation is triggered by a surge in progesterone which occurs during the menstrual cycle.
This surge is caused by the follicle stimulating hormone, which is produced by the pituitary gland. The FSH encourages the growth of follicles in the ovaries, which produce estrogen. As the follicle matures, estrogen levels peak. The peak in estrogen causes the brain to secrete luteinizing hormone, which triggers the follicle to rupture and release an egg (ovulation). Activin, inhibin B, and a gradual decrease in estrogen levels are all part of the process that precedes and follows ovulation. Activin is a hormone secreted by the ovaries, which helps to mature follicles.
Inhibin B is a hormone secreted by the ovaries, which is thought to help control the amount of FSH in the body and in turn the number of follicles that mature. A gradual decrease in estrogen levels occurs as ovulation approaches and during the luteal phase of the menstrual cycle. This decrease in estrogen helps to prepare the body for the next menstrual cycle.
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you have discovered a new kind of cell with a strange new organelle that contains a highly hydrophobic compartment. which will mostly certainly be abundant in this organelle?
The new organelle that you discovered with a highly hydrophobic compartment will most likely contain lipids, such as fatty acids and phospholipids, as they are hydrophobic molecules.
Which molecule will mostly certainly be abundant in this organelle?There are a number of molecules that will most certainly be abundant in an organelle that contains a highly hydrophobic compartment. In the context of biochemistry, the most abundant molecule is usually the one that is most soluble in the organelle's environment.
According to a number of theories, lipids are most likely to be the most abundant molecules in an organelle containing a highly hydrophobic compartment. Lipids are a diverse class of molecules that are primarily defined by their solubility characteristics. Lipids are soluble in organic solvents and insoluble in water, which means they are ideal for forming membranes, which are hydrophobic compartments.
Therefore, lipids will most certainly be abundant in an organelle that contains a highly hydrophobic compartment.
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the provided structure is an aldehyde substrate derivative that specifically inhibits elastase. which elastase active site residue forms a covalent bond with the aldehyde inhibitor?
The aldehyde substrate derivative that specifically inhibits elastase forms a covalent bond with a serine residue in the active site of elastase.
Aldehydes are a class of organic compounds that have a carbonyl group at the end of their carbon chains, denoted as -CHO. Aldehydes have a polar carbonyl group and a nonpolar hydrocarbon region, making them highly reactive. Aldehydes are classified as primary, secondary, or tertiary based on the degree of substitution of the carbon atom attached to the carbonyl group. Elastase is a serine protease enzyme that breaks down elastin, a major protein component of connective tissue in the body, resulting in the disassembly of elastic fibers. Elastase is secreted by neutrophils, monocytes, macrophages, and fibroblasts, among other cells. It plays a vital role in wound healing and inflammation. The aldehyde inhibitor binds to the active site of elastase and forms a covalent bond with a serine residue. The serine residue is part of the catalytic triad (His, Asp, and Ser) that aids in the breakdown of peptide bonds. The covalent bond formed between the aldehyde inhibitor and the serine residue in the elastase active site is irreversible, resulting in enzyme inhibition. Therefore, the serine residue forms a covalent bond with the aldehyde inhibitor.Learn more about aldehyde: https://brainly.com/question/17101347
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which of the following characteristics apply to all species in kingdom protista? group of answer choices eukaryotic unicellular heterotrophic possess cell walls aquatic
The following characteristics apply to all species in the kingdom Protista is eukaryotic. All species in Kingdom Protista are eukaryotic, meaning they have a membrane-bound nucleus and other organelles in their cells.
None of the following characteristics apply to all species in the Kingdom Protista:
Heterotrophic: Some protists are heterotrophic (i.e., they obtain their nutrition from other organisms), but some are autotrophic (i.e., they produce their own food through photosynthesis).Possess cell walls: Some protists have cell walls, but not all. Some have cell membranes only.Aquatic: While many protists are aquatic, some are found in soil, or in the bodies of other organisms.Learn more about Kingdom Protista: https://brainly.com/question/15377222
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the red portion of the human lip: question 12 options: integumentary lip. has no facial markings. must be treated by hypodermic tissue building in every case. mucous membrane.
The red portion of the human lip is known as the mucous membrane. It does not have any facial markings and must be treated by hypodermic tissue building in every case.
The mucous membrane is a layer of tissue that lines various parts of the body's openings and cavities that are in contact with the outside environment. It is a moist membrane that secretes mucus, a slimy substance that assists in trapping germs and other foreign substances, as well as keeping the surface moist.
The red portion of the human lip: Mucous membrane. The red portion of the human lip is the mucous membrane. The mucous membrane of the lips is often known as the vermilion zone. It is a transition zone between the skin and the mucous membrane.
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How is a substitution mutation different from a frameshift mutation? Which one is likely to be more dangerous to an organism? Why?
Answer:
A substitution mutation is a type of genetic mutation where one base pair in the DNA sequence is replaced with a different base pair. This can result in a change in the amino acid sequence of the protein that is translated from the DNA sequence. If the substitution mutation occurs in a non-coding region of the DNA, it may not have any effect on the organism.
On the other hand, a frameshift mutation is a type of genetic mutation where one or more base pairs are inserted or deleted from the DNA sequence. This can shift the reading frame of the DNA sequence, changing the way that the sequence is translated into amino acids. This can result in a completely different protein being produced, or a protein that is missing critical parts or has extra parts that don't function properly.
In general, frameshift mutations are likely to be more dangerous to an organism than substitution mutations. This is because frameshift mutations can result in a completely different protein being produced, or a protein that is missing critical parts or has extra parts that don't function properly. This can have a significant impact on the function of the protein, which can in turn impact the health and survival of the organism. Substitution mutations, on the other hand, may result in a change to a single amino acid in the protein, which may or may not have a significant impact on its function.
However, it is important to note that the impact of a mutation on an organism depends on a variety of factors, including the location of the mutation, the function of the protein that is affected, and the specific genetic and environmental context in which the organism exists. Therefore, it is not always the case that frameshift mutations are more dangerous than substitution mutations, and the impact of a particular mutation must be evaluated on a case-by-case basis.
Which of the following is NOT found in saliva? A) urea and uric acid. B) electrolytes. C) lysozyme. D) protease. D) protease.
Proteases enzyme is not found in saliva , hence option 'D' is correct
The natural execration occurs from salivary gland, thus it accounts for high concentration of urea and uric acid found in saliva. Since the amount of creatinine production is consonant in 24 hours , uric acid and urea -to- creatinine ratio are better to clarify the changes of this compound concentration in saliva . Therefore option A is incorrect.
The main inorganic components are sodium , potassium, chloride, calcium, phosphate , and bicarbonate , all contributing to the ionic strength of saliva. Therefore option B is incorrect.
As an important part of the non specific immune defense mechanism , lysozyme is an important component of antibacterial in saliva. Therefore option C is incorrect.
Proteases are released by pancreas into the proximal small intestine ,where the mix with proteins already denatured by gastric secretion's and break down into amino acids. Therefore option "D" is correct.
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6. What type of body blan do sponges have?
A. Cephalization
B.asymmetry
C.bilateral symmetry
D.radial symmetry
The Option B is correct. The body blan have the assymetry types of sponges in them
What are sponges?Sponges (Phylum Porifera) are a type of aquatic animal that lack true tissues and organs. They are considered the simplest of all animals and do not have a body plan based on symmetry.
Instead, sponges exhibit a type of symmetry known as "asymmetry," which means they have no plane of symmetry or any organization of body parts around a central axis. Therefore, the correct answer is B. asymmetry.
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procaine (novocaine) is metabolized primarily by the group of answer choices liver. lungs. plasma. kidneys.
Answer: plasma
Explanation:
what was the control group in this study? a the transplanted population in the killifish pools b the transplanted population in the pike-cichlid pools c the source population in the killifish pools d the source population in the pike-cichlid pools
In an ecological study involving killifish and pike-cichlid pools, the control group is the source population in the pike-cichlid pools as it did not receive any intervention in the study.
In a study, the control group refers to the group that does not receive any treatment or intervention and is used as a comparison to the experimental group. In this scenario, the source population in the pike-cichlid pools is the control group as it did not receive any intervention in the study. The study is not mentioned in the question, but based on the options provided, it is likely an ecological study involving killifish and pike-cichlid pools. The transplanted population is most likely the experimental group. The source population in the killifish pools and the source population in the pike-cichlid pools are both control groups that did not receive any intervention in the study.
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during conjugation, the donor cell generally retains a copy of the genetic material being transferred. this is termed a blank process
Answer:
Conservative
Explanation:
During conjugation, the donor cell generally retains a copy of the genetic material being transferred. This is termed a conservative process.
the ability to predict the consequence of an action is located in the group of answer choices gustatory cortex. olfactory receptors. left cerebral hemisphere. prefrontal cortex. right cerebral hemisphere.
The prefrontal cortex is where one can forecast how an action will have an effect.
What area of the brain is in charge of anticipating the outcomes of events or actions?A wide range of executive processes are supported by the prefrontal cortex, including: concentrating one's thoughts. anticipating environmental events and anticipating the results of one's actions.
Which region of the brain is in charge of consciousness?The main component of the forebrain, the cerebrum, is the brain (or prosencephalon). The cerebral cortex, which is its dominant outer region, processes sensory and motor information as well as enabling consciousness, or our capacity to think about ourselves and the outside world.
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In the same mouse species, a third unlinked gene (gene C/c) also has an epistatic effect on fur color. The presence of the dominant allele C (for color), allows the A/a and B/b genes to be expressed normally. The presence of two recessive alleles (cc), on the other hand, prevents any pigment from being formed, resulting in an albino (white) mouse.Matchthe phenotypes on the labels at left to the genotypes listed below. Labels can be used once, more than once, or not at all.agoutisolid colorsolid coloragouti blackalbinoAaBbccAaBBCCAabbccAAbbCcaaBbCcAABBcc
The phenotype "agouti" would be matched with the genotype AaBb, "solid color" with the genotype AaBB or Aabb, "black" with the genotype AABB or AABb, and "albino" with the genotype cc. This is because the presence of the gene C/c (epistasis) determines the fur color of the mouse, and the genotypes above show the different combinations of alleles. If two recessive alleles (cc) are present, it will result in an albino (white) mouse.
Explanation:
Physical characteristics like the fur color of a mouse are determined by the combination of genes in the organism's DNA. Epistasis is a phenomenon in which the expression of one gene affects the expression of another gene. When an organism reproduces, genes are inherited by offspring from their parents. In the context of this problem, the genes involved in determining fur color are A/a, B/b, and C/c. C is the gene that has an epistatic effect on fur color.
Here, are the matched genotypes with phenotypes: AaBbcc - agouti solid colorAaBBCC - solid colorAgouti black - AAbbCc, AaBbCcAlbino - aabbcc, aabbCc, aabbCC, aaBbcc, aaBbCc, aaBBcc.The label agouti solid color matches with the genotype AaBbcc. The solid color matches the genotype AaBBCC. The label agouti black matches with the genotypes AAbbCc and AaBbCc. The label albino matches with the genotypes aabbcc, aabbCc, aabbCC, aaBbcc, aaBbCc, and aaBBcc.
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imagine a condition where the vessels that carry blood between the lungs and the body tissues were permeable to oxygen. what would you expect to observe relative to the normal condition of low permeability to oxygen in the vessels that carry blood from the lungs to the tissues?
If the vessels between the lungs and body tissues were permeable to oxygen, there will be a decrease in the oxygen supply to the body tissues.
Normally, oxygen-poor blood from the body tissues flows into the right side of the heart, and is then pumped to the lungs where it picks up oxygen and releases carbon dioxide. The oxygen-rich blood then flows back to the left side of the heart, where it is pumped out to the body tissues to supply oxygen to the cells.
If the vessels between the lungs and body tissues were permeable to oxygen, oxygen-rich blood from the lungs would flow into the right side of the heart, mix with oxygen-poor blood from the body tissues, and then be pumped out to the body tissues.
This would result in a reduced delivery of oxygen to the tissues, as some of the oxygen-rich blood from the lungs would bypass the body tissues and flow back to the lungs.
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describe the zones of the epiphyseal plate and their functions, and the significance of the epiphyseal line.
The epiphyseal plate, also known as the growth plate, is composed of four zones: the resting zone, the proliferative zone, the hypertrophic zone, and the calcified zone. The epiphyseal line, or growth line, is the division between the epiphyseal plate and the diaphysis and is where all growth stops.
The resting zone is the first zone in the epiphyseal plate and is located at the epiphyseal side of the plate. It contains cells that are inactive but can divide to form more chondrocytes, which are essential for the formation of bone and cartilage.
The proliferative zone is the second zone and is the site of cell division and growth.
The hypertrophic zone is the third zone and is the site of most growth. It is also the site of most of the extracellular matrix mineralization, as chondrocytes in this zone produce high levels of collagen and other matrix proteins.
The calcified zone is the fourth and last zone and is composed of cells that are no longer able to divide or grow. It contains mature, mineralized cartilage.
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Which best describes a hurricane?
A
a low-pressure weather system
B
a high-pressure weather system
C
a cold front
D
a stationary front
Answer:
your answer is: A hope this helps
Explanation:
Please help quick I’ll mark brainly
Why does the Northern hemisphere produce more CO2 overall? Why does it absorb more CO2 certain times of year?
Answer:
The Northern Hemisphere produces more CO2 overall for several reasons. One main reason is that it contains more land area and therefore more vegetation that undergoes photosynthesis, which takes in CO2. However, during the winter months, when the temperature drops, the vegetation goes dormant and stops absorbing CO2. At the same time, human activity, such as burning fossil fuels and heating buildings, tends to increase during the winter months, which leads to an increase in CO2 emissions. As a result, the Northern Hemisphere experiences seasonal variations in CO2 levels, with higher levels during the winter months and lower levels during the summer months when vegetation is actively growing and absorbing CO2. Additionally, the Northern Hemisphere experiences more seasonal variation in general, with more extreme temperatures and weather patterns that can affect the balance of CO2 in the atmosphere.
leucine aminopeptidases (laps) are found in all living organisms and have been associated with the response of the marine mussel, mytilus edulis, to changes in salinity. laps are enzymes that remove n-terminal amino acids from protein
Leucine aminopeptidases (LAPs) are a group of enzymes found in all living organisms, including the marine mussel Mytilus edulis. These enzymes play a crucial role in protein metabolism by catalyzing the cleavage of N-terminal amino acids from protein substrates.
LAPs have been implicated in a variety of physiological processes, including protein turnover, regulation of peptide hormone levels, and immune system function. In Mytilus edulis, LAPs have been shown to play a role in the organism's response to changes in salinity. When the salinity of their environment changes,
Mytilus edulis utilizes LAPs to modify the composition of proteins in their cells, allowing them to better adapt to the changing conditions. This adaptation is important for the organism's survival, as changes in salinity can significantly affect the functioning of cells and tissues.
Overall, LAPs are versatile enzymes that play a critical role in protein metabolism and are found in a wide range of living organisms, including the marine mussel Mytilus edulis. Their ability to modify protein substrates makes them important players in many physiological processes, including adaptation to changing environmental conditions.
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meiosis divides one cell into four cells, but the resulting cells have half the amount of dna as compared to the original cell. how do you think this is possible?
During meiosis, one cell is divided into four cells, but the resulting cells have half the amount of DNA as compared to the original cell. This is because of the two cell divisions, meiosis I and meiosis II, that occur during meiosis.
During meiosis I, homologous chromosomes separate, resulting in two cells with half the number of chromosomes as the original cell.
During meiosis II, sister chromatids separate, resulting in four cells, each with half the number of chromosomes as the original cell.
In other words, the resulting cells have half the amount of DNA because meiosis results in four cells, each containing half the number of chromosomes and, therefore, half the amount of DNA as the original cell.
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up to 25% of a cell's atp is used to run sodium-potassium pumps. without the resulting sodium and potassium gradients, neurons and muscles cannot fire properly. if a person is poisoned with cyanide, they cannot generate atp, and die within a few minutes. in relation to the sodium-potassium pump, what specific impact would cyanide have on concentrations across the cell membrane?
Cyanide depolarizes the peritubular cell layer by +18.8 +/ - 2.3 mV/10 min in the presence and by +4.5 +/ - 0.9 mV/10 min without even a trace of the luminal substrate.
Hydrogen cyanide is a poisonous little nonpolar particle that is delivered by certain plants to discourage herbivores. Cyanide crosses layers and restrains a critical cycle in the breath.
The cyanide particle, CN, ties to the iron molecule in cytochrome C oxidase in the mitochondria of the cells and goes about as an irreversible protein inhibitor. This keeps cytochrome C oxidase from doing what it needs to do, which is to send electrons to oxygen in the electron transport chain of high-impact cell breath.
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Help with my biology please
Carbohydrates are composed of monosaccharides, proteins are composed of amino acids, and nucleic acids are composed of nucleotides.
What are the elements present and the building blocks in carbohydrates, proteins, and nucleic acids?Carbohydrates, proteins, and nucleic acids are three major classes of biomolecules that are essential for life.
Here are the elements present and the building blocks of each:
Carbohydrates:
Carbohydrates are organic molecules that contain carbon, hydrogen, and oxygen in the ratio of 1:2:1. The building blocks of carbohydrates are monosaccharides, which are simple sugars that cannot be broken down into smaller molecules. Examples of monosaccharides include glucose, fructose, and galactose.
Proteins:
Proteins are complex molecules that are made up of amino acids. Amino acids contain carbon, hydrogen, oxygen, nitrogen, and sometimes sulfur. There are 20 different types of amino acids, and they are joined together by peptide bonds to form polypeptide chains, which fold into specific three-dimensional structures to form proteins.
Nucleic acids:
Nucleic acids are macromolecules that store and transmit genetic information. They are composed of nucleotides, which are made up of a nitrogenous base, a sugar, and a phosphate group. The four nitrogenous bases in DNA are adenine, guanine, cytosine, and thymine, while in RNA, uracil replaces thymine. The sugar in DNA is deoxyribose, while in RNA, it is ribose. The nucleotides are joined together by phosphodiester bonds to form a linear chain called a polynucleotide.
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in humans, telomerase activity is most likely to be found in which cells? select one: red blood cells germ cells muscle cells all cells neurons
Telomerase activity in humans is most likely to be found in germ cells. The correct answer is b.
Telomerase is an enzyme that adds nucleotides to the ends of chromosomes to prevent them from becoming shorter after every division of the cell. This enzyme is found in some cells, particularly embryonic stem cells, adult stem cells, and cancer cells.
Germ cells are responsible for the creation of sperm and eggs in males and females, respectively. Germ cells are crucial to reproduction, and their genetic makeup is passed on from one generation to the next. When germ cells divide, they undergo many more cycles than other cell types.
As a result, they are more likely to experience telomere shortening, which is why telomerase activity is more common in these cells.
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