Answer:
Errors in the human genetic code, which are called mutations, sometimes lead to the production of abnormal proteins that may cause disease, including autoimmune disease and malignancy.A gene mutation is a permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most people. Mutations range in size; they can affect anywhere from a single DNA building block (base pair) to a large segment of a chromosome that includes multiple genes.
when would a forest be sustainable?
Answer: B: When supply is greater than demand
Explanation:Hope this helps
Which would most likely contribute to better digestion and respiration?
Answer: Energy is released when bonds in the food molecules are broken during digestion.
Explanation:
The G-protein-linked receptor is located in the plasma membrane. When GDP is attached to the G protein the messenger is considered inactive. GTP replaces GDP and now the messenger is considered active. The G protein carrying the GTP leaves the receptor and binds to and enzyme which causes a cellular response. All of this is brought on by a _______ ________ attaching to the G-protein-linked receptor and will shut down quickly when the ___________ ____________ is no longer there.
Answer:
Signal Molecules
Signal Molecules
Explanation:
someone asked this same question and it was answered
Please someone help me please
It is false.
Explanation:
Colloids include gels, sols, and emulsions; the particles do not settle, and cannot be separated out by ordinary filtering or centrifuging like those in a suspension.
In the United States, it is possible for discoverers of gene sequences in organisms to patent those sequences. This gives the discoverer property rights for the sequence. Many scientists object to this practice. Which is the strongest scientific argument against allowing a gene sequence to be patented?
Group of answer choices
Patenting sequences prevents conservationists rom understanding the ecological needs of organisms from which the patented sequences come.
Patenting sequences prevents he sequences from being expressed in nature.
Patenting sequences prevents researchers from studying and creating innovations from the patented sequences.
Patenting sequences prevents the sequences from being used in genetically modified organisms.
Answer:
Explanation:
There is little evidence that early fears about gene patenting placing substantial ... owner and do not protect against independent invention), patents require disclosure that ... gene knock-out methods and even for individual gene sequences. ... Human gene patents result from the cloning and description of the sequence of a ...
so option c maybe
I need help with the answer
Answer:
Carbon Dioxide
Explanation:
The light-independent reactions use the ATP and NADPH from the light-dependent reactions to reduce carbon dioxide and convert the energy to the chemical bond energy in carbohydrates such as glucose.
List three questions you would need to answer in order to support the claims being made about GroBIg
Answer:
Who is grobig
Explanation:
Answer: For production agriculture this generally means supplementing precipitation with irrigation. ... Increases in fuel prices means that pumping extra irrigation water increases irrigation expenses without ... GROBig Red Virtual Learning Series.
in an appropriate design experiment, a scientist is able to test the effect of?
Answer:
This question is incomplete as it lacks options, the options are:
A) a single variable
B) multiple variables
C) the hypothesis
D) scientific observations
The answer is A
Explanation:
An experiment is conducted to solve a particular problem or find answers to a given scientific question. In an experiment, which usually consists of variables, only A SINGLE VARIABLE is tested at once.
This means that the effect of a variable called INDEPENDENT VARIABLE is tested at a time. The independent variable is the variable that is changed or manipulated in an experiment. This means that only a SINGLE VARIABLE can be changed at at time in an an appropriate design experiment.
What are 2 characteristics of Eukaryotes?
Answer:
prokaryotic cells, eukaryotic cells have: a membrane-bound nucleus. numerous membrane-bound organelles (including the endoplasmic reticulum, Golgi apparatus, chloroplasts, and mitochondria) several rod-shaped chromosomes
Explanation:
Answer:
They have a nucleus, They have road shaped chromosomes
Explanation:
why is forcing the cell to increase the rate of the cell cycle lead to error in DNA replication
why do you think we should wear mask?
Answer:
So that we can limit the cases and keep safe :)
Explanation:
Answer:
masks slow the spread of the virus and or prevent you from catching the virus.
What happened if we add normal saline instead of PBS during beta amylase extraction?
Answer:
hi
Explanation:
Saline is the solution of water and NaCl does not provide the appropriate pH, so enzyme activity is lost, we cannot add saline instead of PBS during beta amylase extraction.
How saline water affects beta amylase extraction?PBS (phosphate buffer solution) is a type of buffer that is suited for beta-amylase activity, which implies that when beta-amylase is extracted using buffer, the enzyme's chemical activity is kept.
When we utilize saline, which is a solution of water and NaCl, the pH of the solution is not acceptable, and the enzymes' chemical activity is destroyed.
As a result, for enzyme/protein extraction, we always employ a buffer solution, which maintains the ph for the proper functioning of an enzyme.
Therefore due to pH conditions enzyme lost activity, and normal saline water can not be used instead of PBS for extraction of beta-amylase.
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You need a dog to work with the police.What traits would you want the dog to have? Why?
Listen How are channel and carrier proteins similar? Select all that apply.
A. Channel and carrier proteins move substances in a certain direction, regardless of their concentration gradients.
B. Channel and carrier proteins are both types of facilitated transport.
C. Channel and carrier proteins can only move substances in one direction either into the cell or out of the cell.
D. Channel and carrier proteins always move substances from the side of the membrane with the highest concentration to the side with the lowest concentration.
Answer:
a
Explanation:
A. Channel and carrier proteins move substances in a certain direction, regardless of their concentration gradients.
Channel and carrier proteins are both types of facilitated transport.
Facilitated diffusion is one of the ways of transporting molecules and is characterized by the use of proteins that are inserted in the plasma membrane, such as ion channels and carriers or permeases.
Ions, amino acids and monosaccharides, among many other molecules, cannot cross the plasma membrane, because they are polar or are very large in size.
So, for the cell to obtain or eliminate these substances, the presence of transporter proteins is necessary.
This diffusion is a type of passive transport, because it takes advantage of the concentration gradient of the molecules and does not waste energy.
Ion channels are integral tunnel-shaped proteins, selective for one, two, or three ions. When a channel opens, ions flow under two principles: the concentration gradient and the electrochemical gradient.Consequently, when an ion channel opens, the potential difference between the two compartments is altered.
Transmembrane proteins mediate the transport of molecules such as bicarbonate or large, polar, uncharged molecules such as glucose.The transport through these proteins occurs in favor of the concentration gradient, and by a reversible conformational change of the proteins that allows the translocation of the molecule to the other side of the membrane.
This type of transport is always without energy expenditure and in favor of the electrochemical gradient, it occurs in the following way:
Uniport, a single molecule translocates in only one direction.Simporte, two molecules that translocate in the same direction.Therefore, we can conclude that channel and carrier proteins are both types of facilitated transport.
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An endosperm is the embryo of a plant. False True
Answer:
False
Explanation:
What is biology of brown rat?
ignore how i selected them) PLEASE HELP ME. DO IT CORRECTLY PLEASEEEEEEE
This tutorial will take you step by step through the question.
In cucumbers, dull fruit (D) is dominant to glossy fruit (d), and orange fruit (R) is dominant to cream-colored fruit (r). The gene that codes for dull versus glossy assorts independently from the gene that codes for orange versus cream-colored. A plant that has dull and orange fruits is crossed to a plant that has dull and cream-colored fruits. The cross produces eight total progeny, with three plants that have dull and orange fruits, three plants with dull and cream-colored fruits, one plant with glossy and orange fruits, and one plant with glossy and cream-colored fruits.
Determine progeny phenotypic ratios - texture. To determine the actual genotype of the parents from among the possible genotypes identified in the previous step, separate the cross into two single-locus crosses, looking at the inheritance of each trait by itself. Start with the texture characteristic.
What is the fraction that represents the number of dull progeny?
What is the fraction that represents the number of glossy progeny?
What is the ratio of dull progeny to glossy progeny?
Answer:
The progeny phenotypic ratios for both genes = 3:3:1:1 --> 3/8 Dull and Orange, 3/8 Dull cream, 1/8 Glossy and Orange, 1/8 Glossy and cream. The progeny phenotypic ratios for glossy/dull = 3:1 --> 3/4 Dull fruits, 1/4 Glossy fruitsThe progeny phenotypic ratios for orange/cream = 1:1 --> 1/2 Orange fruits, 1/2 Cream fruitsThe genotype of the parents: DdRr and Ddrrdull progeny: 3/4 = 75% Dull- fuited individualsglossy progeny: 1/4 = 25% Glossy-fruited individualsratio of dull progeny to glossy progeny: 3:1orange progeny: 2/4 = 1/2 = 50% Heterozygous, cream progeny: Rr, Orange-fruited plantsratio orange to green: 1:1Explanation:
Due to technical problems, you will find the complete explanation in the attached files
Calculate the molarity of 0.75 L of a solution containing 0.83 g of dissolved KCI. A 0.015 M B 0.75 M C 1.1 M D 6.2
Answer:
A 0.015M
Explanation:
Molarity, which refers to the molar concentration of a solution, can be calculated using the formula:
Molarity (M) = mole (n) / volume (L)
Based on the information provided in this question, the solution contains 0.83 g of dissolved KCI.
We can calculate the number of moles of KCl in the solution by using the formula:
Mole = mass ÷ molar mass
Where atomic mass of; K = 39, Cl = 35.5
Molar Mass of KCl = 39 + 35.5
= 74.5g/mol.
Mole = 0.83g/74.5g/mol.
mole = 0.01114
Approximately, n = 0.011mol
Hence, molarity = 0.011mol/0.75L
Molarity = 0.0146
Molarity = 0.015M
How does mercury change from something benign to something harmful?
Answer:
Burning coal releases mercury into the atmosphere. It falls into sediments and is converted into methyl mercury by bacteria
Explanation:
4. Take a beaker (jar or jug) with some water and put some drops of red or blue
ink in it. Take a tender twig of any flowery plant with leaves and flowers, preferably
white flowers, and put it in the beaker for 6 to 8 hours. What do you observe? For
further examination cut across its stem and look for the presence of colored water.
Explain your observations.
Answer:
Blue Ink patches are observed on the leaves of the plant. Also, on cutting across the stem of the plant, the red color of the solution is found along the length of the stem.
The above observation shows that the stem of the plant conducts water through its length to the leaves of the plant.
Explanation:
The leaves of plant obtain water and minerals from the soil through the roots of the plant. The water is conducted by the stem of the plant from the roots to the leaves of the plant where they are needed for photosynthesis as well as for cooling the plant. The xylem tissue in plants is responsible for conducting water to the leaves of the plant from the roots of the plant through the stem.
The conduction of water from the roots to the leaves of the plant is maintained by capillary action as well as by transpiration pull. Transpiration pull refers to the pull of water by the transpiration action taking place in the leaves of the pant, whereby water evaporates from the leaves of the plant through the opening in the leaf of the plant.
When the blue ink is added to the water, the colored water is conducted through the stem of the plant to the leaves. On getting to the leaves, the water molecules evaporate leaving behind the colored patches fond on the leaves. When the stem of the plant is cut, the blue color is seen along its length showing that the colored water was conducted through it.
Which of the following best describes a difference between a mutualistic relationship and a parasitic relationship? A. Parasitism harms both organisms, while mutualism harms only one organism. B. Parasitism benefits only one organism, while mutualism benefits both organisms. C. Parasitism involves only two organisms, while mutualism involves many organisms. D. Parasitism continues for many generations, while mutualism is limited to one generation.
Answer:A. Parasitism harms both organisms, while mutualism harms only one organism. B. Parasitism benefits only one organism, while mutualism benefits both organisms.
Explanation:i hope this helps
Original DNA Sequence:
TACACCTTGGC GACGACT
mRNA Sequence:
Amino Acid Sequence:
Explanation:
ATGTGGAACCG CTGCTGA
UTGTGGUUCCG CTGCTGU
In other words, how are we speeding up the effects of the competitive exclusion principle and thereby altering the outcome of that ecosystem's natural succession
Answer: Overgrazing, overfishing, and forest fires
Explanation:
Competitive exclusion principle two species which have the same ecological niche cannot exists together as such species will be competing for the same resources. The species which is superior over the other will receive the resources and the other species having no competitive advantage will not survive in future.
According to the given situation, human being is the most superior species on earth and have competitive advantage of thinking ability and intelligence over other species. Succession are the changes that occur in the biotic community of an ecosystem with respect to time.
The human beings can speed up the effects of the competitive exclusion principle by various ways: Overgrazing, overfishing, and forest fires. The overgrazing of the cattle in the field can remove the vegetation cover of the region and the land will become barren so instead of progressive succession in terms of vegetation cover the succession will again re-initiate in terms of primary succession if environment supports.
Overfishing can cause the exclusion of some valuable species of fish and there will not be evolution of such species and will alter the outcome of natural succession.
Forest fires can affect both floral and faunal species some species may tolerate the fire and will survive and some precursors like roots of the plants can support new individual plants. This will again alter the outcome of natural progressive succession in an ecosystem.
Someone do this plese! will give brainlist and alot of points
Answer:
Hi Hi really sorry may i get some points i need them to give it to other people cuz some people want points, ik its not the answer u wanted sorry but hope u get the answer soon!
Explanation:
What are the two main types of cells and where are they found in the human body?
Answer:
They are prokaryotes and eukaryotes and prokaryotes are single celled and eukaryotes are multi celled
Explanation:
Hope that helps! Have a fantastic day!
The two types of cells found in the human body are blood cells and immune cells.
What are cells?Cells are the fundamental foundations of all life. Trillions of cells make up the human body.
They support the body's structure, absorb nutrients from food, repurpose those nutrients into energy, and perform specialized functions.
Nucleic acids, proteins, carbohydrates, and lipids are the four major classes of organic compounds found in all cells.
A cell is made up of three parts: the cell membrane, the nucleus, and the cytoplasm that lies between the two.
The cytoplasm contains complicated accommodations of fine fibers as well as hundreds or even thousands of tiny but distinct structures known as organelles.
Thus, there can be many cells in a human body, the most important perhaps are blood cells and immune cells.
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Which of these is an abiotic infectious agent?
● Bacteria
●Fungi
● Parasites
● Viruses
Answer:
A. Bacteria
Explanation:
Hope this helps!
Explain why lamarckism is currently not a widely accepted theory
Answer:
Its not really taught in schools that much.
Explanation:
A) Identify a human disorder with developmental limitations that results from changes in chromosome number. Explain how nondisjunction leads to changes in chromosome number.
B) Mutations result in changes to genotype that can result in changes in phenotype. Explain how a mutation causes a change in the genotype of an organism AND may result in a change in the phenotype of an organism.
Answer:A) Patau Syndrome (Trisomy 13) causes intellectual and physical disability, such as underdeveloped eyes, extra fingers/toes, heart defects. Survival beyond the first year is uncommon.
B)
Explanation: Trisomy (or aneuploidy in general) can result when chromosomes to do not separate correctly during mitosis or meiosis. In meiosis, non-separation of a chromosome pair results in a gamete with two copies of the chromosome (and consequently one gamete lacking the chromosome.
At fertilisation the embryonic cell will have three copies of the chromosome (and an embryonic cell with one copy only). These are serious mutations, many of which are non-viable and usually abort spontaneously. Others results in abnormal development and poor survival rates. Only one autosomal trisomy (21) and sex chromosome trisomies (XXX, XXY etc) result in babies that survive into adulthood, albeit with physical and developmental abnormalities (trisomy 21 abd trisomy X). Only one monosomy (XO) is viable.
Other mutations can be less inimical, and may not result in any variation from normal. Mutations in genes coding for proteins or ribosomes may result in potential loss of function. As there are two copies of each gene, the mutated gene is paired with a normal gene and if that is expressed there will be no loss of function.
There are cases where the mutated gene is dominant it will change the phenotype. An example is Marfan Syndrome, an autosomal (chromosome 15) dominant mutation resulting in connective tissue abnormalities and long bones.
An autosomal recessive mutation is not expressed but is carried. If both parents are carriers, the probability of offspring to be doubly recessive and have an altered phenotype is 25%. Cystic fibrosis is an example.
A third possibility is where two alleles are co-dominant. An example of this is sickle cell disease. Consider the three allele pairs SS, Ss and ss.
Those with ss have sickle cell anaemia, a painful and debilitating condition. Those with SS have normal blood cells. Those with Ss have sickle cell trait, which has some mild deficits because a proportion of blood cells are abnormal.
what is sexual reproduction?
Answer:
Hey!
Explanation:
Erm maybe look it up, itll give you a straight answer and I feel like you asked this to see what we answer