what name is given to a gene that causes cancer? what name is given to a gene that causes cancer? repressor promoter oncogene homeotic gene

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Answer 1

The name given to a gene that causes cancer is oncogene.

A gene is a unit of heredity that is transmitted from one generation to the next and is responsible for a particular trait of an organism.

Oncogenes are genes that promote cell growth and division. When they are mutated or expressed at high levels, they can cause normal cells to become cancerous.

There are two types of genes that are involved in causing cancer: oncogenes and tumor suppressor genes.

Oncogenes are genes that promote cell growth and division, and when they are mutated or expressed at high levels, they can cause normal cells to become cancerous.

Tumor suppressor genes, on the other hand, are genes that normally prevent cell growth and division, and when they are inactivated or lost, they can lead to cancer development. Therefore, both oncogenes and tumor suppressor genes are important in cancer biology.

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Related Questions

For male cats

O allele =

o allele =

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Answer:

For male cats, there is only one allele for each gene located on the X chromosome because they only have one X chromosome. Therefore, the O and o alleles, which are variations of the blood type gene, would still be present in male cats but they will only have one copy of it.

The O allele codes for the type A blood antigen, and the o allele codes for the type B blood antigen. When a male cat inherits an O allele from its mother, it will have type A blood, and when it inherits an o allele, it will have type B blood. If the male cat inherits one O allele and one o allele, it will have type AB blood, which is a rare blood type in cats. However, this can only happen if the male cat has a genetic anomaly, such as Klinefelter syndrome, which gives it two X chromosomes instead of one.

Which of the following could be a consequence of global warming ?

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The major effects include decreased food yields and water availability, as well as rising drought risks as well as biodiversity loss, forest fires, & heat waves in global warming.

Several different calamities, such as storms, heat waves, floods, & droughts, are getting worse as a result of rising temperatures. Wet areas get wetter and dry areas become dryer as a result of a warmer climate producing an atmosphere that really can gather, hold, and discharge more water. As greenhouse gases like carbon dioxide and other pollutants build up in the atmosphere, they absorb sunlight as well as other solar rays that have rebounded off the earth's surface and are intended to escape. This process is known as global warming. Changes in precipitation amount and pattern may result from rising global temperatures.

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why won't changing one base letter on a mrna codon always change the amino acid it codes for? give an example

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Changing one base letter on an mRNA codon does not always change the amino acid it codes for because the genetic code is degenerate. This means that more than one codon can code for the same amino acid. For example, UUU, UUC, and UUA all code for the amino acid Phenylalanine. The mRNA codon is read in triplets, or three nucleotide bases, so a single base change in one codon does not necessarily change the amino acid it codes for.


To illustrate this further, let's consider the codons for Alanine. The codons for Alanine are GCU, GCC, GCA, and GCG. Each of these codons contains three nucleotide bases, so even if one of the bases is changed, it still codes for the same amino acid Alanine. In summary, changing one base letter on an mRNA codon does not always change the amino acid it codes for because of the degenerate nature of the genetic code.

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which of the following contains the genetic code, or DNA, of an organism?
#1 diffusion
#2chromosome
#3 nutrient
#4 water molecule

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The genetic code, or DNA, of an organism is contained in the [ chromosome ].



Chromosomes are structures made up of DNA and protein that carry genetic information in the form of genes. living organisms and are involved in many biological processes, but they do not contain genetic information.

the chromosomes (dna) in this cell have been dyed blue and the cytoskeletal components have been dyed green. which phase of mitosis is this cell in?

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This cell is in the metaphase phase of mitosis. In this phase, the chromosomes (dyed blue) are aligned in the center of the cell and the spindle fibers (dyed green) are connecting the chromosomes to the spindle poles.

Phases of Mitosis:

Mitosis is the process of cell division that results in two identical daughter cells. It can be divided into four distinct phases that are discussed below.

Prophase: In this phase, chromosomes condense and become visible. Chromosomes pair up to form an "X" shape, with each pair comprising a pair of sister chromatids. Cytoskeletal structures called microtubules start to form, which will eventually form the spindle apparatus. The nuclear envelope begins to disintegrate.

Metaphase: The chromosomes align at the cell's equator during this stage. The spindle apparatus and microtubules attach to the kinetochores on the chromosomes. The centrosomes migrate to opposite poles of the cell, forming the spindle's poles.

Telophase: The spindle apparatus disintegrates, and new nuclei begin to form at either end of the cell. The chromosomes relax, and their characteristic shape disappears. Cytokinesis, or the splitting of the cell into two daughter cells, begins at this stage.

Anaphase: The sister chromatids are pulled apart and drawn toward the spindle poles during this phase.

The spindle apparatus shortens as microtubules shorten, pulling the chromatids in opposite directions. As a result, each chromatid is now regarded as an individual chromosome. The cell becomes more oval-shaped as the spindle pulls the chromosomes towards the poles until they are completely separated.

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a mutation arises in a gene that codes for a lysosomal hydrolytic enzyme. the mutation changes an amino acid in the active site of the enzyme so the enzyme doesn't function properly. what effect might this mutation have on lysosome function?

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The effect might this mutation have on lysosome function is the lysosome will not be able to digest certain molecules.

Lysosomes аre membrаne-enclosed orgаnelles thаt contаin аn аrrаy of enzymes cаpаble of breаking down аll types of biologicаl polymers: proteins, nucleic аcids, cаrbohydrаtes, аnd lipids.

Lysosomes function аs the digestive system of the cell, serving both to degrаde mаteriаl tаken up from outside the cell аnd to digest obsolete components of the cell itself. In their simplest form, lysosomes аre visuаlized аs dense sphericаl vаcuoles, but they cаn displаy considerаble vаriаtion in size аnd shаpe аs а result of differences in the mаteriаls thаt hаve been tаken up for digestion.

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the life cycles of plant species alternate between haploid and diploid generations. the haploid generation is called the

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The haploid generation is called the gametophyte in the life cycles of plant species that alternate between haploid and diploid generations.

A life cycle is a sequence of developmental stages in the lives of sexually reproducing organisms, from the time they are born until they produce offspring themselves. It involves a series of changes in form and function that are repeated from one generation to the next. The haploid generation, known as the gametophyte, is the phase of the plant life cycle in which the plant produces haploid gametes, which are sex cells with only one set of chromosomes. Gametes from two separate organisms combine during fertilization to form a diploid zygote, which grows into the next phase of the plant life cycle, the diploid generation. The diploid generation, known as the sporophyte, is the stage of the plant life cycle in which the zygote develops into a multicellular organism that produces spores. The spores are haploid and can develop into new gametophytes. This is the beginning of the next haploid generation, and the cycle repeats itself. The life cycle of plants, therefore, is characterized by a regular alternation between diploid and haploid generations.

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during resting, passive exhalation, the internal intercostals would be recruited and contracting. group of answer choices true false

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During resting, passive exhalation, the internal intercostals would not be recruited and contracting. The statement is false.

The internal intercostals muscles are the muscles that form the intercostal muscles of the human body. They are located between the ribs and the sternum. During expiration, the internal intercostal muscles are employed to push the ribcage down, reduce the diameter of the thoracic cavity, and force air out of the lungs during active exhalation.

The following are the functions of the internal intercostals:

To decrease the ribcage width

To compress the thoracic cavity to expel air

To lower the diaphragm

To increase the intrapleural pressure of the thorax

During active expiration, the internal intercostals play an essential role in the ribcage movement. They contract to push the ribcage down, resulting in the diaphragm relaxing, pushing air out of the lungs, and decreasing the size of the thoracic cavity.

During resting, passive exhalation, the internal intercostals are not recruited and contracting. Instead, the elasticity of the lungs and thoracic cage allows air to leave the lungs without any external assistance, resulting in a passive exhalation process. During passive exhalation, the diaphragm and external intercostal muscles are relaxed. Therefore, the statement is false.

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Marine life in the oceans are an important source of atmospheric _______________.

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Marine life in the oceans are an important source of atmospheric oxygen. Marine life refers to the plants, animals, and other organisms that inhabit the ocean or marine biome, and they provide various services such as food, oxygen, medicines, and recreation to humans.

Marine life is crucial to the ocean's functioning, and its diversity is due to the existence of unique organisms that cannot be found elsewhere.

Phytoplankton, which is a significant part of marine life, plays a crucial role in the global carbon cycle by serving as the foundation of many marine ecosystems and transporting carbon from the surface to the deep ocean when they die and sink.

Marine life is essential to mitigating climate change because the ocean absorbs approximately one-third of the carbon dioxide produced by human activities.

Marine life, particularly phytoplankton and seaweed, is responsible for producing roughly 70% of the Earth's oxygen, with land-based plants and trees producing the remaining 30%.

Phytoplankton use photosynthesis to produce oxygen by converting carbon dioxide and water into glucose and oxygen using light energy.

The oxygen produced by marine life is critical to the survival of humans and animals worldwide, and the ocean's oxygen supply is essential for the survival of marine life as well.

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the oxygen exchange between the red blood cells and the alveoli is driven by diffusion. this diffusion is due to the

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The oxygen exchange between the red blood cells and the alveoli is driven by diffusion. this diffusion is due to the lower pressure of oxygen in the red blood cells.

Red blood cells, also known as erythrocytes, are one of the main types of blood cells in the human body. They are responsible for transporting oxygen from the lungs to the body's tissues, and carbon dioxide from the tissues to the lungs for removal. Red blood cells are biconcave discs that are small in size, measuring about 7.5 micrometers in diameter.

They contain a protein called hemoglobin, which binds with oxygen and gives the cells their characteristic red color. Red blood cells are produced in the bone marrow and have a lifespan of about 120 days. They are constantly being produced and broken down in the body, with the spleen playing a major role in removing old or damaged red blood cells.

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a chromosomally normal woman and a chromosomally normal man have a son whos sex chromosome constitution is xxy. in which parent and in which meiotic division did the nondisjunction take place ?

Answers

a. A son whose sex chromosome constitution is XXY from his father.

b. The nondisjunction took place in the second meiotic division

Disorders of chromosome number include the duplicаtion or loss of entire chromosomes, аs well аs chаnges in the number of complete sets of chromosomes. They аre cаused by nondisjunction, which occurs when pаirs of homologous chromosomes or sister chromаtids fаil to sepаrаte during meiosis. The risk of nondisjunction increаses with the аge of the pаrents.

In the case above, both Y chromosomes in the XYY bаby must come from the fаther, so nondisjunction took plаce in the fаther. In normаl meiosis, the first meiotic division sepаrаtes the X chromosome from the Y chromosome, аnd the second meiotic division sepаrаtes the sister chromаtids of the X chromosome аnd the sister chromаtids of the Y chromosome. For the Y chromosomes to remаin together аnd be included in the sаme sperm, nondisjunction must tаke plаce in the second meiotic division.

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Bully whippets are homozygous for a deletion of two base pairs in the myostatin gene. This deletion changes an mRNA codon in the middle of the myostatin mRNA from UGU to UGA. Use your knowledge of the genetic code to determine the effect of this mutation on the structure of the resulting protein.

Answers

Explanation:

The deletion of two base pairs in the myostatin gene in bully whippets results in a frameshift mutation. This means that the reading frame of the mRNA is shifted, causing all subsequent codons to be read incorrectly. The mutation changes an mRNA codon in the middle of the myostatin mRNA from UGU to UGA, which is a stop codon.

UGU normally codes for the amino acid cysteine, but UGA does not code for any amino acid. Instead, it signals the end of the protein chain. Therefore, the mutation results in premature termination of the myostatin protein synthesis.

The resulting protein will be truncated and incomplete, lacking the C-terminal portion of the myostatin protein. This deletion is likely to affect the function of the myostatin protein, which is a negative regulator of muscle growth. As a result, bully whippets have increased muscle mass and strength compared to other whippet breeds.

Answer:

The genetic code is a set of rules that dictates the correspondence between the nucleotide sequence in DNA or mRNA and the amino acid sequence in proteins. Each codon in the mRNA specifies a specific amino acid, and the reading of the codons occurs in sets of three.

In this case, the deletion of two base pairs in the myostatin gene changes an mRNA codon from UGU to UGA. The codon UGU encodes for the amino acid cysteine, while UGA is a stop codon that signals the end of translation. Therefore, the mutation results in a premature termination of translation, leading to the production of a truncated protein that lacks a portion of the myostatin protein's normal sequence.

Since myostatin is a negative regulator of muscle growth, the mutation in the bully whippets leads to a loss of function of the myostatin protein, resulting in increased muscle mass and the "bully" phenotype observed in these dogs.

Compare and contrast Jupiter’s Galilean satellites.

Answers

Answer:

Explanation:

Jupiter is the planet fifth in order from the sun, having an equatorial diameter of 88,729 miles (142,796 km), a mean distance from the sun of 483.6 million miles (778.3 million km), a period or revolution of 11.86 years, and at least 14 moons. It is the largest planet in the solar systems.

Jupiter are at least 80 Galilean moons.

The most known ones are Ganymede, Calisto, Io, and Europa.

Name of Moon               Diameter             Distance from Earth

Ganymede                     3, 273.5               542.44M

Calisto                              2,995.4                   542.44M

Io                                       2,263.8                            542.44M

Europa                               1,939.7                             542.44M

Io-no craters/active volcanoes/no h2o or ice

Europa-no craters/icy w/cracks/geologic activity

Ganymede-icy surface/more craters

Callisto-heavily craters(ice) closer to Jupiter =more geological activity

Thanks.

which term names the broadest, most inclusive taxonomic group? question 4 options: genus species family domain

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The term that names the broadest, most inclusive taxonomic group is domain. The correct option is d.

What is a domain?

In biological taxonomy, a domain is the broadest category into which living organisms can be classified. Domain, Kingdom, Phylum, Class, Order, Family, Genus, and Species are the eight fundamental categories or ranks utilized in the biological classification of all living things.

A domain is a high-level taxonomic category that includes one or more kingdoms. The three domains are Archaea, Bacteria, and Eukarya, with Eukarya being the most recently discovered. Eukarya is the group of organisms that are made up of cells with a nucleus, such as animals, plants, fungi, and protists, while Archaea and Bacteria are the two groups of prokaryotes, which are single-celled organisms that lack a nucleus.

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a lawyer is presenting a hair sample with its corresponding nuclear dna that was found at the crime scene. how will this most likely affect the criminal case?

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Answer:

this will further the criminal case- absolutely! but i would need more context as to how it would further the case. does that make sense?

Explanation:

which groups contains only prokaryotes? question 7 options: domains bacteria and eukarya domains archaea and bacteria domains archaea and eukarya only domain eukarya

Answers

The group that contains only prokaryotes is Domain Bacteria and Domain Archaea.

Prokaryotes are unicellular organisms that lack membrane-bound organelles. The cytoplasm is enclosed by a cell membrane and a cell wall, both of which are thin.

Bacteria and archaea are examples of prokaryotes. Eukaryotes are organisms that have cells with nuclei and other membrane-bound organelles.

A prokaryote is a kind of cell that lacks a nucleus and membrane-bound organelles. Prokaryotes come in a variety of shapes and sizes, including spherical (cocci), rod-shaped (bacilli), spiral (spirilla), and comma-shaped (vibrios).

Prokaryotes are classified into two domains: Bacteria and Archaea. Eukarya is the third domain, and it includes all eukaryotic organisms, including animals, plants, fungi, and protists.

Therefore, the only two domains that include only prokaryotic organisms are Bacteria and Archaea.

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assume that a species has a diploid chromosome number of 24. the term applied to an individual with 25 chromosomes would be .

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An individual with 25 chromosomes would be referred to as aneuploid.

Aneuploidy is a chromosomal abnormality caused by a variation in the number of chromosomes in a cell's nucleus.

When compared to the diploid chromosome number, which is the standard chromosome number for an organism, it can either have more or fewer chromosomes than normal.

Diploid chromosome number is the number of chromosomes in the somatic cells of an organism. Diploid chromosomes can be found in organisms that reproduce sexually.

When gametes join during fertilization, the diploid chromosome number is returned to the offspring. The chromosome number is the same in both parents.

The haploid number of chromosomes is the number of chromosomes in the gametes. The haploid number of chromosomes is half that of the diploid chromosome number.

For example, if an organism's diploid chromosome number is 24, it has 12 haploid chromosomes.

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1. Why do Peru and Africa have different amounts of copper deposits?

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Peru and Africa have different amounts of copper deposits due to differences in geologic history and tectonic activity.

The Andes Mountains, which run through Peru, were formed by the collision of the South American and Nazca tectonic plates. This collision caused the Earth's crust to buckle and fold, creating the conditions for the formation of large copper deposits. In contrast, Africa's copper deposits were formed through a variety of processes, including sedimentary and hydrothermal processes.

Additionally, the African continent has undergone multiple tectonic events throughout its history, which have impacted the distribution and formation of copper deposits. Other factors, such as climate and erosion, can also play a role in the distribution of copper deposits. Therefore, the geologic history and tectonic activity of a region are important factors in determining the amount and location of copper deposits.

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what incubation temperature is preferred for the growth of most medically important bacteria? (select all that apply)

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The preferred incubation temperature for the growth of most medically important bacteria is 37°C.

Thus, the correct answer is 37°C (A).

Why is 37 degrees Celsius the optimаl incubаtion temperаture?

The аir in the incubаtor wаs kept аt 37 degrees Celsius, the sаme temperаture аs the humаn body, аnd the incubаtor mаintаined the аtmospheric cаrbon dioxide аnd nitrogen levels necessаry to promote cell growth.

In аccordаnce with the Аssociаtion for the Аdvаncement of Medicаl Instrumentаtion recommendаtions аll cultures should be incubаted аt 37 degrees C for 48 h on suitаble culture mediа, such аs Trypticаse soy аgаr, stаndаrd methods аgаr, or one of severаl commerciаlly аvаilаble аssаy systems. There hаve been suggestions thаt lower temperаtures аnd longer incubаtion might improve the recovery of bаcteriа from wаter аnd diаlysаte.

Your question is incomplete, but most probably your options were

a. 37°C

b. 25°C

c. 45°C

d. 98°C

Thus, the correct option is A.

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if a nondisjuctin offurs in humans for sister chromatids of one of the chromosome during meiosis ii will any normal gametes result? what chromosome number woudl each gamete have?

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If a nondisjunction occurs in humans for sister chromatids of one of the chromosomes during meiosis ii there will be no normal gametes result. The chromosome number would depend on the type of non disjunction occurring.

A nondisjunction occurs when sister chromatids of one of the chromosomes fail to separate during meiosis II. As a result, no normal gametes will result, since each gamete will have either one extra or one missing chromosome. The chromosome number of each gamete would depend on the chromosome that experienced the nondisjunction.

For example, if the nondisjunction occurred on chromosome #7, then each gamete would either have one extra chromosome #7 or one missing chromosome #7.
This is because nondisjunction causes the chromatids of one chromosome to move to the same pole, leaving the other pole with one less chromosome or one extra chromosome. In either case, the chromosome number of the gametes would be different from the chromosome number of the parent cell. This is known as aneuploidy and can lead to serious health issues in the offspring.
Overall, when a nondisjunction occurs in humans for sister chromatids of one of the chromosomes during meiosis II, no normal gametes will result and each gamete will have a different chromosome number than the parent cell. This can lead to serious health issues in the offspring and is known as aneuploidy.

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the of a human begins with the production of gametes by and the consecutive growth of the organism because of .

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The life cycle of a human begins with the production of gametes by meiosis and the consecutive growth of the organism because of mitosis.

Meiosis is a cell division process that occurs in sexually reproducing organisms. It occurs in the reproductive organs of animals, the ovaries in females and the testes in males, and in the reproductive structures of plants. Meiosis is a process that reduces the number of chromosomes in a cell by half in preparation for fertilization.

Mitosis is the process by which a cell divides to produce two identical daughter cells. Mitosis is a fundamental process in the growth and development of multicellular organisms. During mitosis, the cell's nucleus divides, and the chromosomes are separated into two identical sets of chromosomes, each in its own nucleus. Mitosis plays a significant role in the growth and development of multicellular organisms.

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the scientific discipline of classifying organisms into increasingly more inclusive groups according to an international classification standard is known as what

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The scientific discipline of classifying organisms into increasingly more inclusive groups according to an international classification standard is known as taxonomy. The international classification standard referred to in the question is the Linnaean system of classification.

Taxonomy is the scientific practice of naming, defining, and classifying groups of biological organisms on the basis of shared characteristics. Taxonomic categories can range from the most general, such as a kingdom, to the most specific, such as a particular species. It is important to remember that all living organisms can be divided into a series of increasingly more inclusive groups, ranging from kingdom down to species. For example, humans are classified as Homo sapiens, which is part of the genus Homo, the family Hominidae, the order Primates, the class Mammalia, the phylum Chordata, and the kingdom Animalia. In addition, taxonomy provides an internationally accepted system for categorizing organisms, allowing for easier identification, understanding, and comparison.

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when an allotetraploid (aabb) is backcrossed to one of its progenitor diploid species (aa), a sterile offspring is produced. the genomic composition of this sterile individual is best represented by

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When an allotetraploid (aabb) is backcrossed to one of its progenitor diploid species (aa), the resulting sterile offspring will have a genomic composition of AaBb.

During the backcross, the progenitor diploid species contributes one set of chromosomes (aa) while the allotetraploid contributes two sets of chromosomes (aabb). The resulting offspring will have one set of chromosomes from the diploid species and two sets of chromosomes from the allotetraploid.

However, since the genomic composition of the allotetraploid is AABB, and the resulting offspring only inherited one set of chromosomes from each parent, it will have an AaBb genomic composition. This genotype results in a sterile offspring due to the inability of the homologous chromosomes to pair during meiosis, leading to an uneven distribution of chromosomes in the gametes.

Therefore, the sterile offspring resulting from the backcross between the allotetraploid (aabb) and one of its progenitor diploid species (aa) will have a genomic composition of AaBb.

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2. they describe conjugation (matings) done in liquid media where the recipient cells used to be on a biofilm and compared them with matings done with cells still on a biofilm. why did they do these by, at least, triplicate?

Answers

Conjugation in liquid media was performed in triplicate to ensure a consistent and reliable result. By performing the experiment multiple times, it allows for the possibility to compare and contrast the effects of the mating in different scenarios.

Furthermore, it provides a better understanding of the behavior of the recipient cells when they are no longer in the biofilm. For instance, the researchers may be able to measure the relative fitness of the cells when they are in liquid media compared to when they are still in the biofilm.

Additionally, replicating the experiment would reduce any variability in the results, ensuring that the conclusions drawn are reliable.  

In summary, performing the conjugation experiment in triplicate allows for a more comprehensive evaluation of the effects of the mating, as well as provide a better understanding of the behavior of the recipient cells in different environments.

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Which lightning rod would be best for the building
A-the dog shaped lightning rod it has the most popular shape
B-the triangle shaped lightning rod it is easy to see
C-the heart shaped lightning rod it needs the shortest wire to connect to the ground
D-the line shaped lightning rod it attracts the largest number of lightning strikes

Answers

Answer:

D

Explanation:

The reason is that the line-shaped rod though it attracts lighting the lightning strikes does not affect the building

true or false: as an adult, if you had to choose only one of these two foods (corn or beans) to provide you with essential amino acids, you would choose corn, because it provides more essential amino acids than beans.

Answers

if you had to choose only one of these two foods (corn or beans) to provide you with essential amino acids, you would choose corn, because it provides more essential amino acids than bean is a false statement.

Although corn does provide more essential amino acids than beans, neither of these foods alone is sufficient to provide your body with all of the essential amino acids. To obtain all of the essential amino acids, you would need to include a variety of different plant-based proteins in your diet, such as lentils, nuts, quinoa, and chickpeas.

 

For example, corn is high in leucine and tryptophan, but it does not contain methionine and cysteine, which are essential amino acids found in beans. Beans, on the other hand, are a good source of methionine and cysteine, but they lack other essential amino acids such as threonine, isoleucine, and lysine.

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all hormones are all hormones are proteins. chemical messengers. steroids. cholesterol based. inorganic compounds.

Answers

All hormones are chemical messengers. The correct option is b.

Hormones are signaling molecules produced by glands in the endocrine system and released into the bloodstream to regulate various physiological processes in the body.

Hormones are classified into different categories based on their chemical composition, but not all hormones are proteins or steroids. Hormones can also be made up of other organic or inorganic compounds, depending on their structure and function. Therefore, option B, chemical messengers, is the correct answer to the given question.

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type iii hypersensitivity is caused by soluble antigen-antibody complexes that avoid being phagocytized by macrophages. true false g

Answers

Type III hypersensitivity is caused by soluble antigen-antibody complexes that avoid being phagocytized by macrophages. This statement is true.

What is type III hypersensitivity?

Type III hypersensitivity occurs when a large amount of antigen enters the body and combines with an antibody, forming an insoluble complex. These are difficult to eliminate, and they begin to settle in the tissues, particularly those with a low blood supply and a high concentration of protein. They elicit an inflammatory response and, as a result, the release of proteases, hydrolases, and complement factors is increased.These immune complexes can become stuck in blood vessels or other organs, resulting in symptoms such as joint pain, fever, and rash. These symptoms usually manifest in the tissues where the complexes are deposited.

What are the causes of type III hypersensitivity?

The causative agents of Type III hypersensitivity are usually proteins, such as serum proteins or microbial proteins, that combine with specific antibodies to form circulating immune complexes. If the immune complexes become deposited in the blood vessels, they can result in vasculitis, inflammation, and subsequent tissue damage. Type III hypersensitivity is responsible for diseases like systemic lupus erythematosus, rheumatoid arthritis, and serum sickness.

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you must directly expose cells to the uv light when attempting to disinfect because: (select all that apply) group of answer choices uv does not penetrate surfaces uv does not pass through plastic uv does not penetrate through the air uv does not pass through glass uv works best when not in direct contact with the cell

Answers

The correct answers are: Ultraviolet light does not penetrate surfaces.

UV does not pass through plastic.

UV does not penetrate through the air.

UV does not pass through glass.

In order to disinfect, cells must be directly exposed to UV light. UV does not work well when it is not in direct contact with the cell. Additionally, there are surfaces that UV light cannot penetrate, such as glass and plastic.

What is ultraviolet radiation (UV)?

UV radiation is a form of electromagnetic radiation that is not visible to the human eye. It falls between visible light and X-rays on the electromagnetic spectrum. The sun is the most common natural source of UV radiation, but it can also be found in man-made sources like tanning beds and lamps. When exposed to too much UV radiation, it can cause sunburn, premature skin aging, and skin cancer.

What is the disinfecting effect of UV light?

Ultraviolet light is a potent disinfectant. Because of this, UV light is commonly used to disinfect surfaces and drinking water. When UV radiation penetrates a cell's outer membrane and comes into touch with the DNA inside the cell, it can damage and break the DNA strands. When a cell's DNA is damaged, it cannot replicate and, as a result, dies. This makes UV light a highly effective disinfectant.

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in addition to regulating body fluids and electrolytes, the kidneys endocrine function in maintiaing bone calcium levels consists of what process

Answers

The kidney's endocrine function in maintaining bone calcium levels consists of the process of: vitamin D activation.

The kidney's endocrine function in maintaining bone calcium levels consists of the process of vitamin D activation. The kidneys have three critical functions: regulating body fluids and electrolytes, eliminating waste and toxins, and secreting hormones. The endocrine function of the kidneys includes the secretion of erythropoietin, renin, and prostaglandins.

The kidneys also play a crucial role in the regulation of bone metabolism. Vitamin D is a steroid hormone that plays a critical role in calcium and bone homeostasis. Vitamin D is formed in the skin upon exposure to ultraviolet B radiation or consumed through the diet. Vitamin D requires activation, which occurs in two steps in the liver and kidney.

Vitamin D binds to vitamin D-binding protein in the bloodstream and is transported to the liver. The liver hydroxylates vitamin D at the 25-carbon position, creating 25-hydroxyvitamin D, which is the primary circulating form of vitamin D.

The 25-hydroxyvitamin D is transported to the kidney, where it undergoes a second hydroxylation reaction, creating the active form of vitamin D, 1,25-dihydroxyvitamin D [1,25(OH)2D]. 1,25(OH)2D is the biologically active form of vitamin D that regulates bone calcium homeostasis.

It does so by increasing calcium absorption in the small intestine, mobilizing calcium from bone, and increasing calcium reabsorption in the kidney. In summary, the kidney's endocrine function in maintaining bone calcium levels consists of the process of vitamin D activation.

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