The dominant biochemical activity of the Sickle Cell Anemia Hemoglobin Subunit beta-protein (P68871) is oxygen binding and transport.
The Sickle Cell Anaemia Haemoglobin Subunit beta-protein (P68871) is expected to transport oxygen. Red blood cells deliver oxygen from the lungs to the tissues via haemoglobin. Sickle Cell Anaemia occurs when the beta-globin component of haemoglobin is substituted from glutamic acid to valine. These aberrant haemoglobin molecules can polymerize and twist red blood cells into sickle shapes, causing problems.
The beta-globin subunit of haemoglobin has several important regions, including heme-binding sites for oxygen binding, interface regions for subunit interactions, and the amino acid residue at position 6 (glutamic acid in normal haemoglobin, valine in sickle cell haemoglobin) that is critical for Sickle Cell Anaemia pathology. Red blood cells sickle due to valine substitution at position 6.
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Homologous DNA recombination:
A)Requires 5'-end generation at double-stranded DNA breaks
B)Occurs at the tetrad stage during meiosis
C)Is responsible for transposon movement in human cells
D)Repairs mutations caused by deamination events
E)Inverts DNA sequences as a mechanism to regulate genes
Homologous DNA recombination repairs mutations caused by deamination events. The correct option is (D).
Homologous recombination is the exchange of genetic information between two DNA molecules with high sequence similarity. This can occur during normal DNA replication in dividing cells, but the process is usually regulated to ensure that accurate copies are made and the genome remains stable.
During homologous recombination, a broken DNA molecule is repaired using a template DNA molecule that has the same or very similar sequence. The two DNA molecules are aligned, and sections are swapped between the two, resulting in a complete, unbroken DNA molecule.
A mutation is a change in DNA sequence that may occur naturally or be induced by external factors such as radiation, chemicals, or other environmental agents. Deamination is a type of mutation that can occur when a nitrogenous base is changed to a different base through the removal of an amine group. For example, cytosine can be deaminated to uracil, which is normally found only in RNA. If this change occurs in a DNA molecule, it can lead to problems with replication and transcription, which may result in genetic disorders or diseases.
Homologous recombination can be used to repair mutations caused by deamination events by providing a template DNA molecule with the correct sequence. When a broken DNA molecule is repaired using homologous recombination, the template DNA molecule is used to fill in the missing or damaged sections of the broken DNA molecule. This ensures that the correct sequence is restored, and any mutations caused by deamination or other factors are repaired.
Thus, the correct option is D.
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need answer in 10minutes pleaseeee
Impurity species are present in which of the following defects? Select one or more: A. Boundary defect OB. Vacancy defect □ C. Substitutional defect OD. Interstitial defect
Impurity species can be present in substitutional defects and interstitial defects. Therefore, impurity species can be present in both substitutional defects and interstitial defects, where foreign atoms or extra atoms of different species occupy lattice positions in the crystal structure.
A substitutional defect occurs when an atom in the crystal lattice is replaced by a different atom. This replacement can result in impurity species being introduced into the crystal lattice. For example, if a small percentage of impurity atoms, such as foreign elements, replace the original atoms in the crystal lattice, it creates a substitutional defect with impurity species present.
On the other hand, an interstitial defect occurs when an extra atom occupies an interstitial site within the crystal lattice. This extra atom may be of a different species than the original atoms, resulting in the presence of impurity species within the crystal lattice.
Boundary defects, such as grain boundaries or phase boundaries, are interfaces between different regions of a material and do not directly involve the presence of impurity species. Vacancy defects occur when atoms are missing from their lattice positions, but they do not involve the introduction of impurity species either.
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What test could you use to differentiate between Staphylococcus and Streptococcus?
a. coagulase
b. oxidase c.catalase
d. urease
e. TSI slant Question 48 2.5pts What is the term for the number of virions released from an infected host cell? a.plaque forming unit b.virus forming unit c.phage forming unit
d. burst size e.blowout size
To differentiate between Staphylococcus and Streptococcus, the catalase test is commonly used.
c. catalase
Staphylococcus species are catalase-positive, meaning they produce the enzyme catalase, which can break down hydrogen peroxide into water and oxygen. When hydrogen peroxide is added to a colony of Staphylococcus, it will produce bubbles or effervescence due to the release of oxygen gas.
Streptococcus species, on the other hand, are catalase-negative, meaning they do not produce the catalase enzyme. When hydrogen peroxide is added to a colony of Streptococcus, no significant bubbles or effervescence occur.
Therefore, performing the catalase test can help differentiate between Staphylococcus and Streptococcus.
Regarding question 48, the term for the number of virions released from an infected host cell is:
d. burst size
Burst size refers to the number of new viral particles (virions) released from an infected host cell during the lytic cycle of viral replication. When the host cell lyses or bursts open, the newly formed virions are released and can go on to infect other cells. Burst size can vary depending on the specific virus and host cell interaction.
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1 pts Arrange the following correct sequence of events during exhalation: 1. Air (gases) flows out of lungs down its pressure gradient until intrapulmonary pressure is 0 (equal to atmospheric pressure
Air flows out of the lungs during bin the following correct sequence of events:
1. Contraction of the diaphragm and external intercostal muscles reduces intrapleural pressure.
2. Decreased intrapleural pressure causes the lungs to recoil, compressing the air within the alveoli.
3. The compressed air flows out of the lungs down its pressure gradient until intrapulmonary pressure is 0, equal to atmospheric pressure.
During exhalation, the primary muscles involved are the diaphragm and the external intercostal muscles. These muscles contract, causing the volume of the thoracic cavity to decrease. As a result, the intrapleural pressure within the pleural cavity decreases. The decreased intrapleural pressure leads to the recoil of the elastic lung tissue, which compresses the air within the alveoli.
As the volume of the thoracic cavity decreases, the pressure within the alveoli increases. This increased pressure creates a pressure gradient between the lungs and the atmosphere. The air naturally flows from an area of higher pressure (within the lungs) to an area of lower pressure (outside the body) until the pressures equalize. This process continues until the intrapulmonary pressure reaches 0, which is equal to atmospheric pressure.
Overall, the sequence of events during exhalation involves the contraction of the diaphragm and external intercostal muscles, the recoil of the lungs, and the resulting flow of air out of the lungs down its pressure gradient until the intrapulmonary pressure matches the atmospheric pressure.
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UESTION 46 Clinical microbiologists commonly encounter both yeast and bacterial cells in specimens obtained from patients. Which of the following characteristics are unique to yeast and would thus allow differentiation from bacteria? Choose ALL correct answers. Da Presence of a nucleus b. Round shape c. Presence of a cell wall d. Reproduction by budding
The answer would be A and D.Clinical microbiologists are accustomed to encountering both yeast and bacterial cells in specimens received from patients. The characteristics that are unique to yeast and would allow differentiation from bacteria are:
Presence of a nucleus Reproduction by budding Yeast is a fungus that belongs to the kingdom Fungi and has a membrane-bound nucleus that encloses DNA. Yeast reproduces by budding. In other words, a new cell grows off the side of a parent cell. This budding process, which does not involve binary fission, can give rise to colonies of yeast, which are made up of many individual cells.Cell Wall Presence of a cell wall is not unique to yeast, bacteria, plants, and fungi all have cell walls. Therefore, the answer would be A and D.According to the provided options, the answer to the question is:
Presence of a nucleus and Reproduction by budding.
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Which statement about Mitosis is correct?
At the end of mitosis there is four different daughther cells
At the end of mitosis there is four identical daughther cells
At the end of mitosis there is two different daughther cells
At the end of mitosis there is two identical daughther cells
The correct statement about mitosis is that (D) at the end of mitosis, there are two identical daughter cells. During mitosis, the replicated chromosomes align and separate, ensuring that each daughter cell receives a complete set of chromosomes.
Mitosis is a process of cell division in which a single cell divides into two identical daughter cells.
This process occurs in various stages, including prophase, metaphase, anaphase, and telophase. At the end of telophase, the cytoplasm divides through cytokinesis, resulting in the formation of two separate cells.
These daughter cells contain the same genetic information as the parent cell and are identical to each other. Mitosis plays a crucial role in growth, tissue repair, and asexual reproduction in organisms.
Therefore, (D) at the end of mitosis, there are two identical daughter cells is the correct answer.
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When an organism is exposed to a pathogen for the second time. O memory cells O macrophages O stem cells O complement proteins The type of immune response that is the same for any pathogen is O innate immunity. O adaptive immunity. O passive immunity. O allergic immunity.
Memory cells are crucial in mounting a rapid immune response during re-infection, while adaptive immunity is the type of immune response that is specific to any pathogen.
When an organism is exposed to a pathogen for the second time, memory cells play a crucial role in mounting a rapid and specific immune response. These specialized cells retain information about the previous encounter with the pathogen and can quickly recognize and respond to it upon re-infection.
The type of immune response that is the same for any pathogen is adaptive immunity. Unlike innate immunity, which provides immediate, non-specific defense mechanisms against a wide range of pathogens, adaptive immunity is highly specific and develops over time. It involves the activation of B cells and T cells, which produce antibodies and coordinate cellular responses to eliminate the pathogen.
This immune response is characterized by memory formation, allowing for a faster and more efficient response upon subsequent encounters with the same pathogen.
Macrophages also play a crucial role in both innate and adaptive immunity. They are part of the innate immune system and function as phagocytes, engulfing and destroying pathogens. Additionally, they interact with T cells to initiate adaptive immune responses and present antigens to activate specific immune cells.
Stem cells, on the other hand, are unspecialized cells that have the potential to develop into various cell types. While they are essential for replenishing and maintaining the immune cell population, they are not directly involved in the immune response to a pathogen.
Complement proteins are a group of proteins that work together to enhance the immune response. They play a role in both innate and adaptive immunity by facilitating the destruction of pathogens, promoting inflammation, and assisting in the clearance of immune complexes.
However, they are not specific to the immune response upon re-infection with a particular pathogen.
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You are looking at the color of scales in lizards and find that yellow lizards (Y) are dominant to green lizards (y). However, a second gene, H, controls whether the color will be expressed in the scales. If the lizard is hh, the lizard will always be white, because the pigment does not go into scales. What type of epistasis does this situation represent? a.Dominant epistasis
b. Complimentary (or Double Recessive) gene interaction c.Dominant (or Polymeric) gene interaction
d. Duplicate (dominant epistasis) e.Recessive epistasis f.Dominant suppression
A second gene, H, controls whether the color will be expressed in the scales. If the lizard is hh, the lizard will always be white, because the pigment does not go into scales. option e. Recessive epistasis is the correct answer.
The type of epistasis that the given situation represents is Recessive epistasis. Epistasis is the gene interaction in which the alleles of one gene affect the expression of the alleles of another gene. Recessive epistasis occurs when the homozygous recessive condition of one gene masks the expression of the alleles of another gene. Hence, the given situation represents recessive epistasis.Therefore, option e. Recessive epistasis is the correct answer.
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what is virus host interaction ? i dont find clear info. i have assingment ant i dont know what i write please helppppp
Virus-host interaction refers to the relationship and interactions between a virus and its host organism. It involves the complex interplay between the virus and the host's cells, tissues, and immune system.
During virus-host interaction, viruses infect host cells and hijack their cellular machinery to replicate and produce new virus particles. The virus enters the host's cells, releases its genetic material (DNA or RNA), and takes control of the cellular processes to produce viral proteins and replicate its genetic material.
This can lead to various consequences for the host, ranging from mild symptoms to severe diseases.
The host organism's immune system plays a crucial role in the virus-host interaction. It detects the presence of viruses and mounts an immune response to eliminate the infection.
The interaction between the virus and the host's immune system can result in a dynamic battle, with the virus trying to evade the immune response and the immune system attempting to control and eliminate the virus.
The outcome of virus-host interaction can vary depending on factors such as the virulence of the virus, the host's immune response, and the specific mechanisms employed by the virus to evade or manipulate the host's defenses.
Understanding virus-host interactions is essential for developing strategies to prevent and control viral infections.
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D the fog 0 f mercy, Grihan with the aan A per with mood has which of the following antibodustume the has been powd to the Code all that aply ADA Abo Ah it to which blood type is considered the universal donor? Why can this blood type be given to all other blood which blood type is considered the universal recipient? Why can people with this blood type receive From all other blood types? Exploring Anatomy & Physiology in the Laboratory
The blood type that is considered the universal donor is O-negative blood. This is because O-negative blood doesn't have any antigens that could provoke an immune response from the recipient.
Therefore, it can be given to people with any blood type. On the other hand, the blood type that is considered the universal recipient is AB-positive blood. This is because AB-positive blood doesn't have any antibodies that could attack donor blood cells.
Therefore, people with AB-positive blood can receive blood from all other blood types. It's important to note that although O-negative blood is the universal donor, it's still important to test the recipient's blood for other factors such as Rh factor, since this can also impact the compatibility of the blood transfusion.
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Question 13 0.05 pts Which of the following mechanisms produces the MOST diversity in T cell receptors? imprecise joining of VDJ segments O having multiple V region segments from which to choose somatic hypermutation having multiple C region gene segments from which to choose Question 17 0.05 pts Which statement BEST DESCRIBES the function of the C3 component of complement? It forms part of a convertase on the bacteria and is recognized by neutrophils through the receptor CR1. It binds to antibody Fc that are bound to the surface of the bacteria. It initiates the end-stage of complement to form part of the Membrane Attack Complex (MAC). O It initiates the extrinsic pathway of coagulation
13. Imprecise joining of VDJ segments. The answer 1 is correct.
20. IgE and mast cells. The option 4 is correct.
17. It initiates the end-stage of complement to form part of the Membrane Attack Complex (MAC). The option 3 is correct.
Question 13: The mechanism that produces the MOST diversity in T cell receptors is the "imprecise joining of VDJ segments." This process involves the rearrangement of variable (V), diversity (D), and joining (J) gene segments during T cell development.
Question 20: An inflammatory response that occurs immediately upon exposure to antigen is MOST LIKELY to be mediated by "IgE and mast cells." IgE antibodies are specialized immunoglobulins that are involved in allergic and immediate hypersensitivity reactions.
Upon exposure to an antigen, IgE antibodies bind to mast cells, which are present in tissues throughout the body.
Question 17: The function of the C3 component of complement is BEST DESCRIBED by the statement "It initiates the end-stage of complement to form part of the Membrane Attack Complex (MAC)." The complement system is a part of the innate immune response and plays a crucial role in host defense against pathogens.
C3 is a central component of the complement cascade. Activation of C3 leads to the formation of C3 convertase, which cleaves C3 into C3a and C3b.
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What are some of the components of the body's innate immunity
needed for the adaptive immune response?
The components of the body's innate immunity needed for the adaptive immune response the adaptive immune response, enabling the specific recognition and elimination of pathogens by adaptive immune cells such as T and B cells.
The components of the body's innate immunity that are needed for the adaptive immune response include:
1. Antigen-presenting cells (APCs): Innate immune cells such as macrophages, dendritic cells, and B cells can act as APCs. They capture antigens from pathogens and present them to T cells, initiating the adaptive immune response.
2. Toll-like receptors (TLRs): These receptors are present on various cells of the innate immune system and recognize specific molecular patterns associated with pathogens. TLR activation triggers the production of cytokines and co-stimulatory molecules that enhance the adaptive immune response.
3. Natural killer (NK) cells: NK cells are a type of lymphocyte that play a crucial role in innate immunity. They can directly kill infected or abnormal cells and produce cytokines that influence the adaptive immune response.
4. Complement system: The complement system consists of a group of proteins that can be activated in response to pathogens.
It helps in the opsonization and destruction of pathogens, enhances phagocytosis, and facilitates the recruitment of immune cells to the site of infection, thus supporting the adaptive immune response.
5. Inflammatory response: The innate immune response involves the release of inflammatory mediators such as cytokines, chemokines, and acute-phase proteins.
These molecules recruit immune cells to the site of infection, promote tissue repair, and create an environment favorable for the adaptive immune response.
These components of innate immunity contribute to the initiation and modulation of the adaptive immune response, enabling the specific recognition and elimination of pathogens by adaptive immune cells such as T and B cells.
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Name a plant in TSG where aspects of its growth and/or reproduction are likely to have evolved over time due to selective pressures imposed specifically by humans. Note that here we are discussing evolution in a plant population over multiple generations, not just changes in how one individual plant grows based on how humans manipulate it. Address multiple features that are likely to have been selected for or against, and describe how that is manifested by the individual specimen(s) you observed today.
The Taman Sari Garden is a popular tourist spot located in the Yogyakarta Special Region of Indonesia. It is an excellent example of how human activity can alter plant evolution through selective pressures.
The following is a plant in the TSG where aspects of its growth and/or reproduction have evolved over time due to selective pressures imposed specifically by humans:Frangipani is a plant species in TSG whose evolution has been significantly influenced by human activities. This plant is common in TSG, and it has been bred over time to produce flowers with a wide range of colors.
As a result of selective breeding, the size of the flower has grown larger, and its scent has become more fragrant. These characteristics make it a popular garden plant, and the selective pressures imposed by human preferences have driven its evolution.Frangipani's flowers are large, fragrant, and brightly colored.
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Submit your answer to this question in order to open week 5 lessons page. Complete the table: Cellular location Cellular location Uses Main products produced at the Process in prokaryotic in eukaryotic oxygen cells cells end Glycolysis Intermediate step (prep for Krebs cycle) Krebs cycle Aerobic electron transport chain
The table compares the cellular locations, uses, and main products produced at various stages of cellular respiration in prokaryotic and eukaryotic cells.
In prokaryotic cells, glycolysis occurs in the cytoplasm, where glucose is converted into pyruvate, producing a small amount of ATP and NADH. The intermediate step, also known as the preparatory step for the Krebs cycle, takes place in the cytoplasm as well, where pyruvate is converted into acetyl-CoA.
In eukaryotic cells, glycolysis also occurs in the cytoplasm, generating ATP and NADH from glucose. However, the intermediate step takes place in the mitochondria, where pyruvate is transported and converted into acetyl-CoA.
The Krebs cycle, also known as the citric acid cycle or the tricarboxylic acid cycle (TCA cycle), takes place in the mitochondrial matrix of both prokaryotic and eukaryotic cells. It generates high-energy molecules such as NADH, FADH2, and ATP through a series of enzymatic reactions.
The aerobic electron transport chain, which is the final stage of cellular respiration, occurs in the inner mitochondrial membrane of eukaryotic cells and the plasma membrane of prokaryotic cells. It involves the transfer of electrons from NADH and FADH2 to oxygen, generating a large amount of ATP through oxidative phosphorylation.
Overall, cellular respiration is a crucial metabolic process in both prokaryotic and eukaryotic cells, enabling the production of ATP and the efficient utilization of energy from glucose in the presence of oxygen.
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Which of the following is an important test before you can proceed with identifying an unknown to be Staphylococcus or Streptococcus?
Group of answer choices
Coagulase test
Catalase test and Gram staining
Blood agar test
Catalase test
Gram staining
Before proceeding with identifying an unknown microorganism as Staphylococcus or Streptococcus, it is important to carry out the catalase test.
When there is the identification of an unknown bacterial species, it is important to identify some specific characteristics of the bacteria. The catalase test helps in distinguishing between Staphylococcus and Streptococcus. These two species can be differentiated based on their reaction to the catalase test.The catalase test is a test that is used to differentiate between bacteria that produce catalase and those that do not.
Catalase is an enzyme that helps to break down hydrogen peroxide (H₂O₂) into water (H₂O) and oxygen (O₂). The catalase test helps in differentiating between Staphylococcus and Streptococcus. This is because Streptococcus species lack catalase while Staphylococcus species have catalase activity. The test is performed by placing a small amount of bacterial culture onto a clean glass slide, adding hydrogen peroxide to the slide, and then observing the reaction.
If bubbling is observed, it means that the bacteria species have catalase activity and it is identified as a Staphylococcus species. If no bubbling is observed, it means that the bacterial species do not have catalase activity and it is identified as a Streptococcus species. Therefore, before proceeding with identifying an unknown microorganism as Staphylococcus or Streptococcus, it is important to carry out the catalase test.
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In 2015, on a field trip to the Daintree rainforest you discovered a population of a new species of butterfly. On this field trip you noticed that there were three colour phenotypes within the population; red, pink and white. You observed that the total population consisted of 75 individuals; 16 red, 14 pink and 45 white individuals. During that field trip, you collected some individuals and returned to FedUni. A series of subsequent test crosses in your laboratory revealed that red individuals were homozygous (genotype CRCR), pink individuals were heterozygous (CRCW) and white individuals were homozygous (CWCW). Answer the following questions using the information above: a) As a percentage, what is the frequency of each allele in the population? Include the formula you used to calculate this answer Upon returning to the population a few years later, you notice that the allele frequencies are approximately the same relative to the first time you visited the butterfly population. b) Has this population violated Hardy-Weinberg equilibrium? What does that tell you about the population? c) In 2-4 sentences, describe how the introduction of a new predator that causes a severe decline in the population size and a genetic bottleneck may cause the allele frequencies in this population to change
The frequency of the red allele is 46 / (46 + 104) = 0.
a) to calculate the frequency of each allele in the population, we can use the allele counts provided. the formula for allele frequency is:
allele frequency = (number of copies of the allele) / (total number of alleles)
For the red allele (c), we have 16 homozygous red individuals (crcr) and 14 heterozygous pink individuals (crcw), which makes a total of 2 * 16 + 14 = 46 copies of the red allele.
for the white allele (w), we have 45 homozygous white individuals (cwcw) and 14 heterozygous pink individuals (crcw), which makes a total of 2 * 45 + 14 = 104 copies of the white allele. 307, or 30.7%.the frequency of the white allele is 104 / (46 + 104) = 0.693, or 69.3%.
b) to determine if the population has violated hardy-weinberg equilibrium, we need to compare the observed genotype frequencies with the expected frequencies based on the allele frequencies. in this case, we know the allele frequencies remain approximately the same across visits.
the expected genotype frequencies in hardy-weinberg equilibrium can be calculated using the following formula:
expected frequency = (frequency of one allele)² + 2 * (frequency of one allele) * (frequency of the other allele)
using the allele frequencies we calculated in part (a), we can calculate the expected genotype frequencies. for example, the expected frequency of red homozygotes (crcr) would be:
expected frequency of crcr = (0.307)² = 0.094, or 9.4%.
if the observed genotype frequencies significantly deviate from the expected frequencies, then the population has violated hardy-weinberg equilibrium. however, without the observed genotype frequencies from the subsequent visit, we cannot definitively determine if the population has violated equilibrium.
c) the introduction of a new predator causing a severe decline in population size can lead to a genetic bottleneck. a genetic bottleneck occurs when a population undergoes a drastic reduction in size, reducing genetic diversity. in this scenario, the allele frequencies may change due to random fluctuations and the loss of certain alleles through the bottleneck event. the surviving individuals will have a limited genetic pool, and some alleles may become more or less frequent by chance alone. as a result, the population may experience a shift in allele frequencies and a decrease in genetic variation, potentially impacting the phenotypic diversity observed in the butterfly population.
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One way of identifying a drug target in a complex cellular extract is to use an affinity approach, i.e. fix the drug to a resin (agarose etc) and use it to "pull down "" the target from the extract. What potential problems do you think may be encountered with attempting this approach?
One way of identifying a drug target in a complex cellular extract is by using an affinity approach which involves fixing the drug to a resin such as agarose. The target is then "pulled down" from the extract.
However, this approach may encounter some potential problems such as:
Non-specific binding: The drug resin could bind to other molecules that are unrelated to the target protein, leading to inaccurate results.Difficulty in obtaining a pure sample: Even though the target molecule could bind to the drug resin, other proteins and molecules can also bind which makes it challenging to obtain a pure sample.Low Abundance Targets: In a complex cellular extract, the target molecule may exist in low abundance and the signal might not be strong enough to detect, making it difficult to pull down.Biochemical Incompatibility: The drug and the resin may not be compatible with the target, thus it may not bind or bind weakly which means the target protein might not be able to be pulled down.Therefore, while the affinity approach is a very useful and important method for drug target identification, it also has its limitations and potential problems that need to be considered.
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Question 5 Which mechanism prevents an ovum from being fertilized by multiple sperm cells? Not yet answered Marked out of 1.00 O a. Once a sperm penetrates the jelly-like coating of the egg, no other sperm cells can penetrate the coating. P Flag question b. When more than a single sperm cell fuses with the plasma membrane, multiple zygotes can form, leading to the conception of twins or triplets. O c. The egg can only survive in the Fallopian tube for 24 hours as it does not have mitochondria to produce energy. O d. When a sperm fuses with the plasma membrane of the egg, depolarization of the membrane occurs.
When a sperm fuses with the plasma membrane of the egg, depolarization of the membrane occurs prevents an ovum from being fertilized by multiple sperm cells. The correct option is D.
The correct mechanism that prevents an ovum from being fertilized by multiple sperm cells is the depolarization of the plasma membrane of the egg upon fusion with a single sperm.
When a sperm successfully fuses with the egg's plasma membrane, it triggers a series of changes in the egg, including the release of calcium ions and the depolarization of the membrane. This depolarization creates a fast block to polyspermy, preventing other sperm cells from binding and fusing with the egg.
The depolarization of the membrane initiates several biochemical events within the egg, including the formation of a fertilization envelope and the cortical reaction, which further block the entry of additional sperm.
These mechanisms ensure that only one sperm can successfully fertilize the egg, preventing the formation of polyspermic zygotes and maintaining the genetic integrity of the resulting embryo.
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What type of tissues?
ID on models (torso, digestive system, half head) Oral cavity (mouth), tongue, teeth, sublingual gland, hard palate, soft palate, uvula, submandibular gland, diaphragm, liver, gallbladder, ascending c
The mentioned structures consist of various types of tissues. These include epithelial tissue in the oral cavity, tongue, and glandular tissues; muscle tissue in the tongue, diaphragm, and ascending colon; and connective tissue in the hard palate, soft palate, uvula, liver, and gallbladder.
The tissues mentioned are found in various systems of the body:
1. Oral cavity (mouth): Consists of epithelial tissue, connective tissue, and specialized tissues such as taste buds.
2. Tongue: Comprised of skeletal muscle tissue covered by epithelial tissue.
3. Teeth: Consist of specialized tissues, including dentin, enamel, and cementum.
4. Sublingual gland and submandibular gland: Exocrine glands that contain glandular epithelial tissue.
5. Hard palate and soft palate: Composed of a combination of epithelial tissue and connective tissue.
6. Uvula: Consists of connective tissue and muscle fibers.
7. Diaphragm: A muscle made up of smooth and skeletal muscle tissue.
8. Liver: Composed of hepatocytes, which are specialized epithelial cells.
9. Gallbladder: Contains epithelial tissue for absorbing and concentrating bile.
10. Ascending colon: Part of the large intestine, consisting of smooth muscle tissue.
It is important to note that these tissues collectively make up the structures mentioned, each with their specific composition of cells and extracellular matrix.
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What does the term endocrine mean? What is a hormone? Give 3 examples. 2 What is the meaning of - acromegaly, cretinism, myxedema, euthyroid 3. If a child is born with an insufficient amount of growth hormone, he or she will develop dwarfism. Do you think that such a child should be given supplemental growth hormone? Why or why not?
What does the term endocrine mean?The term endocrine refers to the glands in the human body that produce hormones.
These hormones are produced by these glands and released into the bloodstream to help control the body's growth, development, metabolism, and other functions. Hormones are chemical messengers that are produced by the endocrine system.
What is a hormone? Give 3 examples.A hormone is a chemical that is produced by the body that regulates various functions.
Three examples of hormones are:Insulin: It is produced by the pancreas and helps regulate glucose levels in the body.Thyroxine: It is produced by the thyroid gland and helps regulate metabolism.
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For many medical conditions, adult stem cells are not suitable for treatment so researchers aim to use embryonic stem cells. Compare and contrast the advantages and disadvantages of both adult and embryonic stem cells in cell- based regenerative therapies. Your answer should demonstrate a detailed knowledge of both embryonic and adult stem cell sources, their isolation and characterisation. Your answer should also address the potential ethical and political issues related to stem cell research. (10 marks)
Embroynic and adult stem cells both have advantages and disadvantages in the cell-based regenerative therapies.
Below are some of the comparisons and contrasts:
Embryonic stem cells :Embryonic stem cells are derived from the inner cell mass of blastocysts that have been fertilized by in vitro fertilization (IVF) procedures or cloned by somatic cell nuclear transfer (SCNT).
Advantages: Embryonic stem cells have a high potential to differentiate into any type of cells in the human body and they can divide indefinitely, therefore, can be used to develop any type of cell to regenerate tissues for therapeutic use.
Disadvantages: One of the major disadvantages of embryonic stem cells is their potential to form tumors when transplanted in the human body. They require the administration of immunosuppressive drugs to reduce the risk of rejection. Adult stem cells are present in various organs, tissues, and blood of the human body. They can be isolated from bone marrow, blood, adipose tissue, and other organs.
Advantages: Adult stem cells are present in an already developed organ so they do not require the destruction of an embryo, hence there are no ethical issues involved in their usage. They can be obtained from the patient's own body, therefore, there are no issues of immune rejection. They also have a low risk of tumor formation when used for therapeutic purposes.
Disadvantages: Adult stem cells have limited differentiation potential. they can differentiate only into a limited number of cell types. Also, the number of adult stem cells in the human body decreases with age, which can limit their potential to be used in regenerative therapies. The ethical and political issues relating to stem cell research are complex and require a careful consideration of the interests of patients, scientists, and society as a whole.
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Both the extrinsic and intrinsic activation pathways of procoagulation converge to activate _________________ which subsequently converts fibrinogen into fibrin, among its many functions.
O Von Willebrand Factor
O Factor XIII
O Protein C
O Thrombin
O Factor V
Both the extrinsic and intrinsic activation pathways of procoagulation converge to activate thrombin which subsequently converts fibrinogen into fibrin, among its many functions. So, the correct option is Thrombin.
What is thrombin?Thrombin is a protease enzyme that can cleave and activate numerous clotting factors, as well as fibrinogen and factor XIII, among other proteins. It is critical in the coagulation process, which is the body's natural way of stopping bleeding.
The formation of thrombin occurs through the activation of either the intrinsic or extrinsic coagulation pathway. Prothrombin is transformed into thrombin through a complex series of intermediate reactions that necessitate the involvement of other coagulation factors.
Thus, the correct option is Thrombin.
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RNA-seq can be performed using total RNA or mRNA. Explain the difference in terms of sample preparation and the type of results you will obtain and one example where you would prefer one versus the other
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While looking for RFLP markers in the human genome, two scientists use the same 1kb probe and the same set of genomic DNA samples from three generations of a family. Using Southern blots, one scientist discovers a RFLP, while the other does not. Both of their experiments were technically successful in that each step in their experiments was done correctly. What was the difference between the two experiments such that they produced different outcomes?
The most likely difference between the two experiments that led to different outcomes is the presence of genetic variation or mutations within the restriction sites recognized by the restriction enzyme used in the RFLP analysis.
Restriction Fragment Length Polymorphism (RFLP) analysis relies on the use of restriction enzymes to cut DNA at specific recognition sites. These enzymes recognize specific DNA sequences and cleave the DNA at or near these sites. The resulting DNA fragments can then be separated and visualized using techniques like Southern blotting.
In the case described, both scientists used the same 1kb probe and the same set of genomic DNA samples from three generations of a family. The presence of genetic variation or mutations in the restriction sites within the samples could result in different outcomes.
It is possible that the RFLP discovered by one scientist corresponds to a polymorphic site, meaning that some individuals in the family have different DNA sequences at that particular locus. This genetic variation would result in different restriction patterns, allowing the RFLP to be detected in one experiment but not in the other.
The difference between the two experiments and their outcomes likely stems from genetic variation or mutations within the restriction sites targeted by the restriction enzyme, leading to different RFLP patterns.
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Write down your PBD Code: 1ZOY Write down the protein sequence number of your amino acid: 50
Write down what this amino acid was mutated to: ARG
Describe in your own words the enzymatic function of your protein (1ZOY)
ii. Explain the structure of the protein 1ZOY in regards to (primary, secondary, tertiary)
iii. Describe why the position in your protein is important (50) and outline the effects the mutation (ARG) will have on the 3D structure and function of your protein
The replacement of Asp50 by Arg will result in steric hindrance due to the larger size of the Arg side chain compared to the Asp side chain, resulting in a misaligned catalytic site, which will prevent substrate binding and catalytic activity.
PBD Code: 1ZOYProtein sequence number of amino acid: 50Mutated amino acid: ARG Enzymatic Function of protein (1ZOY):The protein with PBD code 1ZOY is L-aspartate oxidase. L-aspartate oxidase is an enzyme that catalyzes the conversion of L-aspartate to iminoaspartate using oxygen as a co-substrate. It plays a significant role in purine biosynthesis and also contributes to uric acid production.
This enzyme has both oxidation-reduction and oxygen-binding activities. The structure of the protein 1ZOY in regards to primary, secondary, tertiary:1ZOY has a polypeptide chain folded into a single domain. It has a well-defined α/β/α sandwich motif, which is a characteristic of a family of enzymes that includes lactate oxidase.
This protein has an additional short C-terminal tail, which differs from lactate oxidase. The α/β/α sandwich motif is a recurring pattern of secondary structure that is a hallmark of several structural protein folds and enzymes. The primary structure of the protein refers to its amino acid sequence, while the secondary structure refers to the local conformation of the chain.
The tertiary structure refers to the folding of the entire protein molecule. Describe why the position in your protein is important (50) and outline the effects the mutation (ARG) will have on the 3D structure and function of your protein: The amino acid at position 50 of the protein 1ZOY is a catalytically critical residue. It interacts with the substrate and plays a crucial role in catalyzing the reaction.
The mutation of this amino acid from aspartate to arginine would result in a loss of function of the enzyme since it affects the catalytic activity of the enzyme. Hence, it can be concluded that the mutation of Asp50 to Arg would result in a loss of enzymatic activity and would lead to a structural distortion of the protein.
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what is the purpose for ihc staining of uromodulin in the
kidney?
Immunohistochemical staining (IHC) is used to visualize specific molecules in tissue sections. Uromodulin is a protein that is exclusively expressed in the kidney's thick ascending limb of Henle (TAL) and the early distal tubule, where it is secreted into the urine.
The function of uromodulin (UMOD) in the kidney is not fully understood. UMOD is thought to play a role in the formation of the loops of Henle and the recycling of electrolytes and water in the kidney. Mutations in UMOD are associated with autosomal dominant tubulointerstitial kidney disease. Uromodulin expression has been shown to be decreased in a variety of renal pathologies.
Immunohistochemical staining for uromodulin is used to assess its expression levels in the kidney, which can aid in the diagnosis of renal diseases.The staining can be used to visualize the expression of uromodulin and assess the quantity of protein in specific regions of the kidney. This information can be used in the diagnosis of renal diseases. Uromodulin staining can also be used to determine the extent of kidney damage and the efficacy of treatments.
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and on 1111 Prompts: 1. List and describe some of the features that all cells have in common. Consider how you could use these features to determine whether the pathogen was a cell or a virus. (Rememb
Cell features (membrane, genetic material, reproduction) aid in distinguishing cells from viruses based on membrane presence, genetic material type, and reproduction method.
1. Cell Membrane: All cells possess a cell membrane that serves as a protective barrier and regulates the transport of substances. Viruses lack a cell membrane and instead have a protein coat called a capsid.
2. Genetic Material: Cells contain genetic material in the form of DNA or RNA. DNA carries the instructions for cell functioning and heredity. Viruses can have DNA or RNA as their genetic material, but their genome is typically smaller and simpler compared to cells.
3. Reproduction: Cells have the ability to reproduce independently through mitosis or binary fission. Viruses, however, cannot replicate on their own and require a host cell to reproduce. They infiltrate host cells, utilize the cellular machinery, and replicate themselves.
By considering these features, it is possible to differentiate between cells and viruses. If a pathogen possesses a cell membrane, has DNA or RNA, and can reproduce independently, it is likely a cell.
Conversely, if it lacks a cell membrane, has a smaller genome, and relies on a host cell for replication, it is likely a virus.
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We have discussed in the importance of pH on each of the nucleotides and the importance of replication fidelity (or accuracy) by DNA polymerases, primarily during nucleotide insertion specificity and the importance of 1) hydrogen bond formation and 2) geometric shape recognition in the DNA polymerase active site. Discuss in detail the role and function behind DNA polymerase ŋ, with a focus on dGTP mis-incorporation. Based on the research article, please also surmise how pH may affect this mis-incorporation by DNA polymerase n.
DNA polymerase η (pol η) is a specialized DNA polymerase involved in the translesion synthesis (TLS) pathway, which allows for replication past DNA lesions, such as those induced by ultraviolet (UV) radiation. One of the primary functions of pol η is to accurately insert the correct nucleotide opposite a UV-induced lesion, particularly a thymine-thymine dimer.
In terms of dGTP mis-incorporation, studies have shown that pol η has a higher propensity to misinsert dGTP opposite an abasic site (a gap left by a damaged or missing nucleotide) rather than the correct nucleotide, dATP. This mis-incorporation can lead to mutagenesis and potentially contribute to the development of cancer.
Research has also indicated that pH plays a significant role in affecting the mis-incorporation by DNA polymerase η. An article published in the Journal of Biological Chemistry (2017) demonstrated that pol η exhibits a higher fidelity (accuracy) for incorporating the correct nucleotide at neutral pH (around 7.4) compared to acidic pH conditions (around 6.8). Lowering the pH resulted in an increased frequency of dGTP mis-incorporation opposite an abasic site.
The influence of pH on dGTP mis-incorporation by pol η can be attributed to the alteration of the active site's electrostatic environment. pH changes can affect the ionization state of amino acid residues within the active site, influencing hydrogen bond formation and geometric shape recognition, which are crucial for maintaining accurate nucleotide insertion. Therefore, acidic pH conditions can disrupt these interactions, leading to an increased likelihood of mis-incorporation.
In summary, DNA polymerase η plays a role in accurate nucleotide insertion opposite UV-induced lesions, with a focus on dGTP mis-incorporation. Studies suggest that pol η exhibits higher fidelity at neutral pH, and acidic pH conditions can increase the likelihood of dGTP mis-incorporation, potentially contributing to mutagenesis. The effect of pH on mis-incorporation is attributed to alterations in the active site's electrostatic environment, impacting hydrogen bond formation and geometric shape recognition.
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What is the purpose of the leaf disk in water only? control infiltrate
Is it possible that photosynthesis is occurring in a leaf that is not floating? Explain this and support your answer with your data.
The leaf disk is essential in the experiment to identify the occurrence of photosynthesis. For example, in a water-only set up, the leaf disk will sink to the bottom. Thus, we can utilize the leaf disk as a control group where no photosynthesis is occurring, and the process is only taking place within the chloroplasts in the presence of light.
Therefore, the purpose of the leaf disk in water only is to serve as a control group in the photosynthesis experiment. It allows us to distinguish and detect the rates of photosynthesis when exposed to different experimental factors.However, photosynthesis can only occur in a leaf that is not floating.
This is because photosynthesis requires a high concentration of light energy, carbon dioxide, and water. These ingredients are found at the surface of the solution since the leaf disks are suspended, as they are lighter than the water, in a lower concentration than what is necessary for photosynthesis to occur.In a water-only experiment, the lack of infiltrate means that the leaf disk does not have the essential carbon dioxide, water, and light energy. Thus, photosynthesis cannot occur in the absence of infiltrate, and the leaf will not float. The infiltrate is crucial as it provides the carbon dioxide and water that facilitate the photosynthesis process to occur in the leaf disk.
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Question 19 1 pts Inflammation within the deep posterior compartment of the leg can cause a painful compartment syndrome because the surrounding fascial septal boundaries cannot accommodate capacitive changes. Which nerve is most likely to become compressed by severe inflammation of the flexor hallucis longus muscle and be responsible for the painful sensations? O Tibial nerve O Superficial fibular nerve O Sural nerve O Deep fibular nerve
Compartment syndrome Compartment syndrome is a painful and dangerous condition caused by pressure buildup within a muscle compartment. It can be life-threatening and requires immediate medical attention.
As pressure increases, blood flow to the muscles and nerves decreases, resulting in severe pain and damage to the tissues. A significant symptom of compartment syndrome is pain that worsens with stretching and movements of the affected muscles.
The leg has four compartments, which are divided by tough fascial membranes. Inflammation within the deep posterior compartment of the leg can cause painful compartment syndrome because the surrounding fascial septal boundaries cannot accommodate capacitive changes.
Nerve compression within the deep posterior compartment of the leg
The deep posterior compartment of the leg contains several structures that can be affected by severe inflammation of the flexor hallucis longus muscle, which can cause nerve compression and painful sensations.
The most likely nerve to be affected is the tibial nerve. It is the largest and most critical nerve within the deep posterior compartment of the leg, which innervates most of the muscles and provides sensory information from the skin on the sole of the foot and the calf muscles.
Other nerves that may be affected include the deep fibular nerve and the sural nerve.
The deep fibular nerve is responsible for dorsiflexion of the ankle and extension of the toes, while the sural nerve supplies the skin on the outer part of the foot and the little toe. In summary, the tibial nerve is most likely to become compressed by severe inflammation of the flexor hallucis longus muscle and be responsible for the painful sensations.
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