In the Khorana experiment, a repeating copolymer of AGC was created. To determine which amino acid would not be found in the final protein encoded by this copolymer, we need to examine the genetic code.
The codon AGC corresponds to the amino acid serine (Ser). Therefore, Ser would be present in the final protein since it is encoded by the copolymer.
Therefore, the correct answer is not c) Ser.Moving on to the second question, the tRNA with the anticodon sequence 5'-CGU would pair with the codon CGU during protein synthesis. Referring to the genetic code, we find that CGU corresponds to the amino acid arginine (Arg).
Therefore, the correct answer is b) Arg.
In summary, the copolymer of AGC would encode for all the amino acids except serine (Ser), and the tRNA with the anticodon sequence 5'-CGU carries the amino acid arginine (Arg).
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Select all the desired qualities for a gene sequence to act as a barcode. O The barcode sequence does not need to be universal; it can be found in some but not all organisms O The barcode sequence needs to be flanked by sequences that are not very different among species, so the barcode stands out as being variable O The barcode sequence needs to be more similar within a species and more different between separate species O The barcode sequence needs to be short enough to be cheap to sequence and long enough to provide differentiating power
O The barcode sequence needs to be conserved or universally found in all organisms O The barcode sequence needs to have very slow rates of neutral change and mutation O The barcode sequence needs to have higher mutation rates and neutral change than most other genes
O The barcode sequence needs to very similar between species and very different between individuals within a species
A gene sequence that acts as a barcode should possess these desired qualities: flanking conserved regions, intra-species similarity, inter-species variation, optimal length, and slow rates of neutral change and mutation.
To serve as a barcode, a gene sequence should possess certain qualities. Firstly, the barcode sequence needs to be flanked by conserved regions, which are sequences that are relatively similar among different species. This allows the barcode sequence to stand out as a variable region, facilitating species differentiation.
Secondly, the barcode sequence should exhibit more similarity within a species and greater variation between separate species. This characteristic enables the barcode to effectively distinguish between different organisms and aid in species identification.
Additionally, the barcode sequence needs to be of an optimal length. It should be short enough to be cost-effective for sequencing, while also being long enough to provide sufficient discriminatory power for distinguishing between species.
Furthermore, the barcode sequence should have slow rates of neutral change and mutation. This ensures that the barcode remains relatively stable over time and doesn't undergo rapid alterations, maintaining its usefulness as a reliable identification tool.
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In humans the nuclear PT1 gene is located on chromosome 8. It’s protein product, pyruvate translocase, transports the product of glycolysis, pyruvate, from the cytoplasm and into the mitochondria via active transport. Thus, this transport allows the rest of cellular respiration to continue in the mitochondria (glycolysis often happens in the cytoplasm). When mutated, pt1 is malformed and cannot consistently transport pyruvate into the mitochondria. This impacts the overall process of cellular respiration.
Growth Deficiency P2 is a disease caused by an individual carrying two copies of the mutated pt1 allele. It is primarily characterized by slow growth in infancy and early childhood.
Jill and Ned have a baby girl named Gwen who has just been diagnosed with Growth Deficiency P2.
1) Wheat plants that are homozygous recessive for pt1 also have slow growth during the early phase of life. The wheat equivalent PT1 gene is located on chromosome 2. Chromosome 3 contains the gene for stalk texture with N denoting the tough allele and n denoting the smooth allele. A wheat plant that has normal growth and a tough stalk is mated with a wheat plant that has poor early growth and a smooth stalk. Their offspring all have normal growth, but half have a tough stalk and half have a smooth stalk. What was the genotype of the normally growing tough stalked parent?
a) PpNn
b) PPNN
c) Ppnn
d) PPNn
2) In wheat plants that are homozygous recessive for stalk texture (nn), the gene is actually transcribed and translated but the resulting amino acid chain never develops into a mature protein. Which of the following gene expression regulation mechanisms is most likely responsible for this?
a) Chromatin modification
b) RNA interference
c) Folding cutting and destroying
d) Inactivation
3) Wheat plants that are homozygous recessive for the pt1 gene have increased susceptibility to infection by the DNA virus WYM. During infection, the viral proteins used to form the capsid are manufactured by
a) The host cell ribosome
b) The virus particle RNA polymerase
Note: There is only options (a) and (b) for this question.
The genotype of the normally growing tough-stalked wheat parent is c) Ppnn. The gene expression regulation mechanism most likely responsible for the lack of protein development in wheat plants homozygous recessive for stalk texture (nn) is a) Chromatin modification. During infection with the DNA virus WYM, the viral proteins used to form the capsid are manufactured by a) The host cell ribosome.
1. The genotype of the normally growing tough-stalked parent is Ppnn.
To determine the genotype of the parent, we need to analyze the offspring. The offspring all have normal growth, but half have a tough stalk (N) and half have a smooth stalk (n). This means that the parent must have contributed a dominant allele for stalk texture (N) to the offspring, resulting in half of them having a tough stalk. Since all the offspring have normal growth, the parent must also have contributed a functional allele for pt1, as growth deficiency is associated with the recessive mutation of this gene.Hence, option (c) is the correct answer.
The genotype of the normally growing tough-stalked parent can be inferred as follows:
All offspring have normal growth, indicating that the parent does not carry the recessive allele for growth deficiency (p).
Half of the offspring have a tough stalk (N), indicating that the parent must carry at least one dominant allele for stalk texture.
Since the parent has a tough stalk, it cannot be homozygous recessive for stalk texture (nn).
2. The most likely gene expression regulation mechanism responsible for the lack of development of the resulting amino acid chain into a mature protein in wheat plants that are homozygous recessive for stalk texture (nn) is Chromatin modification.
Chromatin modification refers to changes in the structure of chromatin, which consists of DNA wrapped around histone proteins. These modifications can affect the accessibility of genes for transcription. In the case of wheat plants homozygous recessive for stalk texture (nn), the gene responsible for stalk texture is transcribed and translated, but the resulting amino acid chain fails to develop into a mature protein.Hence, option (a) is the correct answer.
3. During infection with the DNA virus WYM, the viral proteins used to form the capsid are manufactured by The host cell ribosome.
The host cell ribosome is responsible for protein synthesis, including the synthesis of viral proteins during an infection. Viruses are obligate intracellular parasites and rely on host cells' machinery to replicate and produce viral components. Upon infection with the DNA virus WYM, the viral genetic material (DNA) is transcribed to produce viral messenger RNA (mRNA), which is then translated by the host cell ribosomes into viral proteins. Hence, option (a) is the correct answer.
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Please answer in your own words not from any out sources!
1. Define equilibrium potential of an ion. How is the magnitude
of the equilibrium potential of an ion calculated? (1 point)
2. Name the equil
Equilibrium potential of an ion refers to the voltage where the electrical gradient which forces the ion across a membrane is balanced by the chemical gradient which opposes the motion of that ion.
The magnitude of the equilibrium potential of an ion is determined by the Nernst equation, which considers the concentration gradient of the ion across the membrane.2. The term “equil" could be short for equilibrium, which refers to a state of balance or stability in which opposing forces or influences are equal and counteract each other. It could also be short for equilateral, which describes a shape or figure that has all its sides equal in length and all its angles equal in measure.
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Name only THREE hormones involved in the control of female menstrual cycle and describe their function. you must include their jobs, where are the produced and when and what is the target organ for EACH hormone.
It's important to note that the menstrual cycle is a complex process involving the interplay of various hormones, and these three hormones represent only a fraction of the hormones involved. Other hormones, such as progesterone, also play critical roles in the menstrual cycle.
Three hormones involved in the control of the female menstrual cycle are:
1. Follicle-stimulating hormone (FSH):
- Function: FSH plays a crucial role in the development and maturation of ovarian follicles. It stimulates the growth and development of follicles in the ovaries.
- Production: FSH is produced and released by the anterior pituitary gland.
- Timing: FSH levels rise during the follicular phase of the menstrual cycle, specifically during the first half of the cycle.
- Target organ: The target organ of FSH is the ovaries, where it acts on the follicles to promote their growth and maturation.
2. Luteinizing hormone (LH):
- Function: LH is responsible for triggering ovulation and the subsequent formation of the corpus luteum. It stimulates the release of a mature egg from the ovary.
- Production: LH is also produced and released by the anterior pituitary gland.
- Timing: LH levels surge during the mid-cycle, specifically during the ovulatory phase.
- Target organ: The target organ of LH is the ovaries, where it acts on the mature follicle to induce ovulation and transform it into the corpus luteum.
3. Estrogen:
- Function: Estrogen is a group of hormones, including estradiol, estrone, and estriol, which collectively play a crucial role in regulating the menstrual cycle. Estrogen is responsible for the development of secondary sexual characteristics and the thickening of the uterine lining (endometrium).
- Production: Estrogen is primarily produced by the developing follicles in the ovaries, particularly the dominant follicle.
- Timing: Estrogen levels rise during the follicular phase of the menstrual cycle, leading up to ovulation.
- Target organ: The target organs of estrogen are the reproductive system and other tissues throughout the body. In the uterus, estrogen promotes the proliferation and thickening of the endometrium to prepare for potential embryo implantation.
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The compound erodoxin inhibtis growth of yeast cells. Which process would be most immediately inhibited by erodoxin treatment?
A. Protein transport into the ER
B. Oxidative protein folding in the ER lumen
C. N-linked protein glycosylation in the ER lumen
D. The unfolded protein response
B. Oxidative protein folding in the ER lumen. The correct option is B.
Erodoxin is a quinone compound which is primarily used as an enzyme substrate for monitoring reductase activity. It is a highly water-soluble compound that is redox-active and able to accept and donate electrons in a similar way to flavins. It has been shown that erodoxin is capable of inhibiting the growth of yeast cells.
However, the compound does not inhibit the growth of yeast by interfering with protein transport into the ER, N-linked protein glycosylation in the ER lumen, or the unfolded protein response. It does inhibit the oxidative protein folding in the ER lumen, which would be most immediately affected by erodoxin treatment. This is a critical process that occurs in the endoplasmic reticulum (ER) lumen, where nascent polypeptides are modified to produce correctly folded, functional proteins.
The protein's sulfhydryl groups are oxidized and isomerized during oxidative protein folding, ensuring proper disulfide bond formation and proper protein folding. Erodoxin is thought to function by modifying sulfhydryl groups on proteins, which is thought to be the reason for its antifungal activity. Thus, it can be concluded that the most immediate process to be inhibited by erodoxin treatment is oxidative protein folding in the ER lumen.
Eradoxin inhibits the oxidative protein folding in the ER lumen. The correct option is B.
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Which molecule is regenerated in the final step (step 8) of the citric acid cycle? a.Oxaloacetate
b. Citrate c. Acetyl COA d.Malate e.Succinate
In the final step (step 8) of the citric acid cycle, the molecule that is regenerated is oxaloacetate. The correct option is A.
The citric acid cycle, also known as the Krebs cycle or tricarboxylic acid cycle, is a series of chemical reactions that occurs in the mitochondria of cells. It is an essential part of cellular respiration, where carbohydrates, fats, and proteins are broken down to produce energy in the form of ATP. In step 1 of the citric acid cycle, acetyl CoA combines with oxaloacetate to form citrate.
Through a series of reactions, citrate is metabolized, releasing energy and producing NADH, FADH2, and ATP. Eventually, in step 8, the molecule oxaloacetate is regenerated. Oxaloacetate plays a crucial role in the citric acid cycle as it is the starting molecule for the next round of the cycle. The correct option is A.
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Describe the cellular branch of adaptive immunity and name its key effector cells.
Describe how the two types of MHCs present antigens and summarize how MHCs impact transplant rejection.
Explain the two-signal mechanism of T cell activation and discuss the factors that affect subclass differentiation
The cellular branch of adaptive immunity involves the activation of T cells through antigen presentation, MHC molecules play a critical role in presenting antigens to T cells, and the two-signal mechanism ensures proper T cell activation.
The cellular branch of adaptive immunity involves the activation of T cells, which are key effector cells in this process. T cells play a crucial role in recognizing specific antigens and coordinating immune responses.
The two major types of T cells involved in cellular immunity are helper T cells (CD4+) and cytotoxic T cells (CD8+). Helper T cells help activate other immune cells by releasing cytokines and coordinating immune responses. Cytotoxic T cells directly kill infected or abnormal cells.
Major Histocompatibility Complexes (MHCs) play a critical role in antigen presentation. There are two types of MHC molecules: MHC class I and MHC class II.
MHC class I molecules are found on the surface of all nucleated cells. They present endogenous antigens, such as viral or tumor antigens, to cytotoxic T cells. MHC class I molecules bind to antigenic peptides in the cytoplasm and present them to CD8+ T cells. This interaction helps activate cytotoxic T cells to eliminate infected or abnormal cells.
MHC class II molecules are primarily found on antigen-presenting cells (APCs), including dendritic cells, macrophages, and B cells. They present exogenous antigens derived from pathogens to helper T cells. MHC class II molecules bind to antigenic peptides in endosomes or lysosomes and present them to CD4+ T cells. This interaction helps activate helper T cells to coordinate immune responses and stimulate other immune cells.
In the context of transplant rejection, MHCs play a crucial role. The mismatch of MHC molecules between the donor and recipient can trigger an immune response, leading to rejection of the transplanted organ or tissue. This occurs because the recipient's immune system recognizes the foreign MHC molecules as non-self and mounts an immune response against them.
The two-signal mechanism of T cell activation involves two signals required for the full activation of T cells.
Signal 1 is the interaction between the T cell receptor (TCR) on the T cell and the antigen-MHC complex on the antigen-presenting cell. This interaction provides specificity to the immune response, as the TCR recognizes and binds to a specific antigen-MHC complex.
Signal 2 is the co-stimulatory signal provided by molecules on the surface of the antigen-presenting cell and their corresponding receptors on the T cell. This co-stimulatory signal, such as the interaction between CD28 on the T cell and B7 on the antigen-presenting cell, is crucial for full T cell activation. Without signal 2, T cell activation may be incomplete or result in tolerance or inactivation of the T cell.
Several factors influence T cell subclass differentiation, particularly the cytokine environment present during T cell activation. Cytokines, such as interleukins, can promote the differentiation of CD4+ T cells into different subsets, including Th1, Th2, Th17, and regulatory T cells (Tregs). The specific cytokine milieu determines the functional characteristics of the T cell subset, including their effector functions and roles in immune responses.
Overall, factors such as cytokines influence T cell subclass differentiation, leading to the development of different T cell subsets with distinct functions in immune responses.
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Toxicity is a recessive allele (t) found in a League tournament of 100 players. This is often masked by the tilt-proof/chill allele (T) also found in the population. 36 of the 100 players are found to be toxic. Calculate the number of individuals who are homozygous for the tilt-proof/chill allele in the tournament. Assume the population is in Hardy-Weinberg equilibrium.
A 41
B 64
C 16
D 40
Hardy-Weinberg Equilibrium states that the genetic variation within a population will remain constant from one generation to the next in the absence of disturbing factors, such as selection, mutation, gene flow, or genetic drift.
According to the question, the toxic allele is recessive, therefore it must be homozygous to be shown in an individual. To calculate the number of individuals who are homozygous for the tilt-proof/chill allele.
The formula for allele frequency is:
[tex]P+q=1[/tex] where P is the frequency of the dominant allele and q is the frequency of the recessive allele. We can use the frequency of the toxic allele to calculate the frequency of the tilt-proof/chill allele, as the two must add up to 1.
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Vision and hearing have similar but different pathways to the
cortex of the human brain. Write out the pathways and then explain
how and why the vestibular pathway must track to the
cerebellum.
The pathways for vision and hearing in the human brain have some similarities but also important differences. Here are the general pathways for each sensory modality:
Vision Pathway:
Light enters the eye and is focused by the cornea and lens onto the retina. The retina contains specialized photoreceptor cells called rods and cones, which convert light into electrical signals. The electrical signals are transmitted through the optic nerve. The optic nerve fibers from each eye partially cross at the optic chiasm. The crossed and uncrossed optic nerve fibers form the optic tracts, which continue to the lateral geniculate nucleus (LGN) in the thalamus.
Hearing Pathway:
Sound waves enter the ear and cause vibrations in the eardrum. The vibrations are transmitted through the middle ear bones (malleus, incus, and stapes) to the cochlea in the inner ear. The cochlea is filled with fluid and contains tiny hair cells that convert the vibrations into electrical signals. The electrical signals are transmitted through the auditory nerve. The auditory nerve fibers synapse at the cochlear nuclei in the brainstem.
From the cochlear nuclei, the auditory information ascends through the brainstem to the inferior colliculus and then to the medial geniculate nucleus (MGN) in the thalamus. Finally, the auditory signals are projected to the primary auditory cortex located in the temporal lobe.
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3. Succinctly explain the difference between the leading and lagging strand on the DNA replication diagram. How does the direction in which DNA pol connect nucleotides lead to the differences?
The leading strand is oriented in the same direction as the replication fork, allowing DNA polymerase to synthesize continuously in the 5' to 3' direction whereas the lagging strand is oriented in the opposite direction of the replication fork.
What are leading and lagging DNA strands?During DNA replication, the leading and lagging strands refer to the two strands of the DNA double helix being synthesized in opposite directions.
The leading strand is the strand that is synthesized continuously in the 5' to 3' direction, which is the same direction as the movement of the replication fork. It is synthesized by DNA polymerase in a continuous manner, adding nucleotides one after the other in a smooth process.
On the other hand, the lagging strand is synthesized discontinuously in short fragments called Okazaki fragments. This occurs because DNA polymerase can only synthesize DNA in the 5' to 3' direction. Since the lagging strand is oriented in the opposite direction to the movement of the replication fork, synthesis of this strand occurs in a series of short stretches.
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If you observed the same organism on a prepared slide and a wet
mount, how did the images compare
The images of an organism on a prepared slide and a wet mount are not always the same. Prepared slides show a fixed specimen that is stained, dehydrated, and mounted permanently on a slide, while wet mounts show the organism in a natural state in a droplet of liquid placed on a slide.
Wet mount is usually the first stage in studying a specimen before making a permanent slide or doing other tests that may alter the specimen's natural state. Observing the same organism on a prepared slide and a wet mount does not necessarily produce the same images. Prepared slides offer a permanent, fixed, and stained specimen, while wet mounts provide a dynamic, natural, and unstained organism.
Wet mounts are used to observe living specimens, such as bacteria, yeast, and protozoans, in their natural state. Wet mounts are usually prepared by placing the organism in a drop of water or a similar fluid on a slide, covering it with a coverslip, and then examining it under a microscope. Prepared slides, on the other hand, require a dead and fixed specimen that is stained, dehydrated, and mounted permanently on a slide.
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Which statements are correct about the four macromolecules? Select all that are true.
a. Chitin and peptidoglycan are examples of carbohydrates
b. a main function of protein is long term energy storage
c. monosaccharides are the building blocks of carbohydrates
d. all lipids are composed of fatty acid tails
The correct statements about the four macromolecules are: monosaccharides are the building blocks of carbohydrates, and all lipids are composed of fatty acid tails.
c. Monosaccharides are the building blocks of carbohydrates. Carbohydrates are composed of monosaccharides, which are simple sugars. Monosaccharides can combine to form larger carbohydrate molecules, such as disaccharides (two monosaccharides) and polysaccharides (long chains of monosaccharides).
d. All lipids are composed of fatty acid tails. Lipids are a diverse group of molecules that include fats, oils, phospholipids, and steroids. They are characterized by their hydrophobic nature and insolubility in water. Lipids are composed of various components, but fatty acids are a common structural feature found in most lipids.
The incorrect statements are:
a. Chitin and peptidoglycan are examples of carbohydrates. Chitin and peptidoglycan are not carbohydrates. Chitin is a structural polysaccharide found in the exoskeleton of arthropods and the cell walls of fungi, while peptidoglycan is a structural component of bacterial cell walls.
b. A main function of protein is long-term energy storage. Proteins have various functions, such as enzyme catalysis, structural support, transport, and immune defense. However, long-term energy storage is primarily carried out by carbohydrates (in the form of glycogen in animals and starch in plants) and lipids (in the form of triglycerides). Proteins are not typically used for long-term energy storage.
In summary, the correct statements are that monosaccharides are the building blocks of carbohydrates, and all lipids are composed of fatty acid tails.
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please answer just the answer will like!
If the relative fitness of the A,A, genotype is 0.8, A,A, is 1.0 and A4, is 0.6, what is the mean relative fitness in the population (assuming before selection its frequency was 0.5 and the population
The mean relative fitness of a population is calculated by multiplying the relative fitness of each genotype by its frequency in the population and summing the products.
The formula is:Mean relative fitness = (frequency of A,A, x relative fitness of A,A,) + (frequency of A,A,A4, x relative fitness of A,A,A4,) + (frequency of A4,A4, x relative fitness of A4,A4,)Given that the frequency of A,A, A,A,A4 and A4,A4 was 0.5 before selection, and the relative fitness of A,A, is 1.0.
The relative fitness of A,A,A4 is 0.8 and the relative fitness of A4,A4 is 0.6, we can calculate the mean relative fitness as follows:Mean relative fitness = (0.5 x 1.0) + (0.5 x 0.8) + (0.5 x 0.6)= 0.5 + 0.4 + 0.3= 1.2Therefore, the mean relative fitness in the population is 1.2.
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Pus formation is a Non-specific (in-born, innate) defense of the host (you). True False Question 62 (1 point) ✓ Saved IgE antibodies are involved in hayfever and asthma hypersensitivities. True False
The given statement "Pus formation is a non-specific (in-born, innate) defense of the host" is true.What is pus?Pus is a fluid that forms in the infected tissue as a result of inflammation caused by an infection. It is composed of dead white blood cells, bacteria, and tissue debris.
Pus is made up of various constituents of the immune system, including dead neutrophils (a type of white blood cell) and macrophages. It also contains destroyed tissue debris, as well as living and dead microbes.Innate or non-specific immunity is the body's first line of defense against microbes that cause disease. This sort of immunity is present at birth and does not change throughout one's life span.
Inborn immunity, also known as natural immunity, includes the skin and mucous membranes as barriers to infection.IgE antibodies are involved in hayfever and asthma hypersensitivities. This statement is true. IgE (immunoglobulin E) is an antibody that our immune system produces in response to certain allergens. It is produced by the immune system in response to allergens such as pollen, dust mites, and animal dander, as well as certain foods, venom, and medications.Allergies and allergic asthma are caused by IgE antibodies that have attached themselves to mast cells. When exposed to an allergen, these cells release chemicals that cause allergic symptoms such as itching, redness, and swelling.
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List all the components that directly participate in the
translation elongation step. CHOOSE ALL THAT APPLY
A.IF1, IF2, IF3 XXXXXX
B.GTP C.stop codon D.AUG start codon E.various tRNAs charged wi
GTP, mRNA, various tRNAs charged with their respective amino acids, small and large ribosomal subunits, EF-Tu, EF-G, the start codon AUG, and the stop codon directly participate in the translation elongation step.
Translation is a vital step in gene expression where ribosomes produce a polypeptide chain from the instructions contained within mRNA molecules. Translation elongation is a critical step in this process, which involves the sequential addition of amino acids to the polypeptide chain using aminoacyl-tRNA complexes.
The components that directly participate in the translation elongation step include mRNA, aminoacyl-tRNA, GTP, elongation factors (EFs), and ribosomes.
The large and small ribosomal subunits play a vital role in the elongation step as they contain the A, P, and E sites necessary for tRNA binding and peptide bond formation. Additionally, they participate in the translocation process, which involves the movement of the mRNA and tRNA through the ribosome. GTP and the elongation factors EF-Tu and EF-G, help in ensuring the correct positioning of aminoacyl-tRNA at the A-site and the movement of tRNA molecules through the ribosome to the next elongation step.
Apart from this, the start codon AUG is necessary to initiate the translation elongation process. The various tRNAs are charged with their respective amino acids, which are subsequently added to the growing polypeptide chain. Finally, the stop codon is essential to terminate the translation elongation step.
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You have generated strains of Drosophila melanogaster that are expected to show interesting developmental phenotypes such as misplaced organs in the adult fly. However, some of these phenotypes are not readily seen with light microscopy. You therefore fix each mutant fly. dry it, coat it with a thin layer of gold, and place the entire fly into an electron microscope for viewing. What type of microscope are you using? Write down SEM (Scanning Electron Microscopy) or TEM (Transmission Electron Microscopy) as your answer.
The microscope that is used to view the entire fly after fixing it, drying it, coating it with a thin layer of gold is the Scanning Electron Microscope (SEM).
It is an advanced imaging tool that uses electrons to scan surfaces of solid samples and produce 3D images with high magnification. SEM provides higher resolution images of the sample compared to the light microscope.
A Scanning Electron Microscope is used in many applications such as material science, life sciences, forensics, and geology. It can detect details that are too small to be seen by other microscopy techniques. SEM is based on the use of a focused beam of electrons that scans the surface of the sample.
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"Mitosis
1. How many chromosomes are present in a human somatic cell? In a
gamete?
A human somatic cell typically contains 46 chromosomes (2n), while a human gamete contains 23 chromosomes (n) due to the process of meiosis.
In a human somatic cell, there are typically 46 chromosomes. These chromosomes exist as 23 pairs, with each pair consisting of one chromosome inherited from the mother and one from the father. The total number of chromosomes in a somatic cell is referred to as the diploid number (2n).
In contrast, a human gamete, such as a sperm cell or an egg cell, contains half the number of chromosomes found in a somatic cell. This is because gametes undergo a specialized form of cell division called meiosis, which reduces the chromosome number by half. Therefore, a human gamete contains 23 chromosomes, which is referred to as the haploid number (n).
The difference in chromosome number between somatic cells and gametes is essential for maintaining the correct chromosome number during sexual reproduction and ensuring the proper development of offspring.
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on heating apple juice with benedict's reagent, the
color in the tube change to brick brown. what do you conclude from
this observation
The observation indicates that the reducing sugar, present in the apple juice, reduces the Cu2+ ion present in the Benedict's reagent to Cu+ ion. As a result of this reduction, Cu+ ions combine with oxygen to form a brick-red colored precipitate (Cu2O).
Benedict's reagent is used to test for the presence of reducing sugars. The reaction of reducing sugars with Benedict's reagent results in the formation of a brick-red precipitate. The given statement states that the color of the tube containing apple juice changes to brick brown when heated with Benedict's reagent. This suggests that apple juice contains a significant amount of reducing sugars. Therefore, apple juice contains a significant amount of reducing sugar, such as fructose and glucose, which reduce the copper ion in Benedict's reagent. Hence, the presence of reducing sugars in apple juice can be confirmed using Benedict's reagent. Ans: Thus, it can be concluded that apple juice contains a considerable amount of reducing sugars like glucose or fructose. The change in color from blue to brick brown when Benedict's reagent was added indicates the positive test for reducing sugar in the apple juice.
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The U.S. Food and Drug Administration granted accelerated approval to a treatment for patients whose cancers have a specific genetic feature (biomarker). This is the first time the agency has approved a cancer treatment based on a common biomarker rather than the location in the body where the tumor originated."" What are the implications of this decision for diagnostic companies and for drug developers? Discuss at least one for each industry.
The decision by the U.S. Food and Drug Administration (FDA) to grant accelerated approval to a cancer treatment based on a common biomarker instead of the tumor's origin has significant implications for diagnostic companies and drug developers.
For diagnostic companies, this decision opens up new opportunities. They can now focus on developing and commercializing diagnostic tests that identify the specific genetic feature or biomarker associated with the cancer, rather than solely focusing on the location of the tumor. This shift allows diagnostic companies to tailor their offerings to the growing field of precision medicine, where treatments can be personalized based on the patient's genetic profile. It creates a demand for accurate and reliable biomarker testing, providing diagnostic companies with a broader market and potentially increased revenue.
For drug developers, this decision also presents notable implications. By targeting treatments based on common biomarkers, drug developers can streamline their research and development efforts. Instead of conducting separate clinical trials for each tumor type, they can focus on developing therapies that target specific genetic features shared across various cancers. This approach can potentially accelerate the drug development process, reduce costs, and increase the chances of success in obtaining regulatory approval. Additionally, drug developers can explore repurposing existing drugs that have shown efficacy against the identified biomarker, allowing for faster development and potential cost savings.
In summary, the FDA's decision to approve a cancer treatment based on a common biomarker has significant implications for both diagnostic companies and drug developers. Diagnostic companies can capitalize on the demand for biomarker testing, while drug developers can streamline their efforts and explore new avenues for drug development based on shared genetic features across different types of cancer.
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Replica plating O is useful for identifying auxotrophs in a population of prototrophs O is useful for identifying auxotrophs with penicillin enrichment O is useful for identifying prototrophs from a population of auxotrophs None of the above
Replica plating is useful for identifying auxotrophs in a population of prototrophs. In the replication plating, the bacterial cells are transferred from one plate to another in order to grow in a new environment and create new colonies. The replica plating technique is used to identify auxotrophs in a population of prototrophs.
Auxotrophs are microorganisms that require specific nutrients or growth factors in order to grow. They are unable to synthesize these compounds on their own and need to obtain them from their environment. In contrast, prototrophs are microorganisms that can synthesize all the nutrients they need to grow.
Replica plating is a technique that is used to transfer bacterial colonies from one plate to another. This technique is useful for identifying auxotrophs in a population of prototrophs. Auxotrophs will only grow on plates that contain the specific nutrients or growth factors that they require.
Therefore, if a bacterial colony is able to grow on one plate but not on another, it can be identified as an auxotroph. This technique is also useful for identifying prototrophs from a population of auxotrophs. Prototrophs will grow on all plates, regardless of the nutrients or growth factors present.
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Think about a "genetic experiment" that would be another way of testing the hypothetical pathway for control of stomatal opening. Instead of treating your leaves experimentally, you would use a specific genetic mutant (think of the use of Arabidopsis in experiments show in class) and compare pore opening of it with the response of normal control plants ("wild-type" genotypes). a) Would pores open in the light if there was a mutation in the blue-light receptors photl, phot2? [0.5pts] I (b) What if there was a mutation in the particular type of K* channel in this pathway so that it would not open? [0.75pts] (c) What is there was a mutant K* channel that did not close? [0.75pts]
a) If there was a mutation in the blue-light receptors phot1 and phot2, then pores would not open in the light. Phot1 and Phot2 are photoreceptor proteins responsible for sensing blue light, which is necessary for stomatal opening.
b) If there was a mutation in the particular type of K+ channel in this pathway, so that it would not open, then pores would not open. K+ channels are responsible for transporting potassium ions, which results in the opening of stomata.
c) If there was a mutant K+ channel that did not close, then pores would stay open for a longer duration than in wild-type plants. Mutant K+ channels could keep transporting potassium ions, resulting in longer periods of stomatal opening.
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List 3 pathologies that affect any organ or organ system and (3)
three diseases in relation to your organs and organ systems
Three pathologies that can affect any organ or organ system are inflammation, infection, and neoplasia. Three specific diseases related to specific organs and organ systems are myocardial infarction (heart), pneumonia (respiratory system), and diabetes mellitus (endocrine system).
1. Inflammation: Inflammation is a common pathological process that can affect any organ or organ system. It is a response of the body to injury or infection, characterized by redness, swelling, heat, and pain. Inflammation can occur in various organs, such as the joints (arthritis), lungs (pneumonia), or skin (dermatitis).
2. Infection: Infections are caused by microorganisms such as bacteria, viruses, fungi, or parasites, and they can affect any organ or organ system. Examples include urinary tract infections (affecting the urinary system), pneumonia (affecting the respiratory system), or gastrointestinal infections (affecting the digestive system).
3. Neoplasia: Neoplasia refers to the abnormal growth of cells, leading to the formation of tumors. Tumors can be either benign (non-cancerous) or malignant (cancerous). Neoplasms can occur in various organs and organ systems, such as breast cancer (affecting the mammary gland), lung cancer (affecting the respiratory system), or leukemia (affecting the blood and bone marrow).
Specific diseases related to specific organs and organ systems:
- Myocardial Infarction: Myocardial infarction, commonly known as a heart attack, occurs when there is a blockage in the coronary arteries supplying blood to the heart muscle. It can lead to damage or death of the heart tissue, resulting in chest pain, shortness of breath, and potential heart failure.
- Pneumonia: Pneumonia is an infection that affects the respiratory system, particularly the lungs. It can be caused by bacteria, viruses, or fungi and results in inflammation and consolidation of lung tissue. Symptoms include cough, fever, chest pain, and difficulty breathing.
- Diabetes Mellitus: Diabetes mellitus is a chronic metabolic disorder that affects the endocrine system, specifically the pancreas. It is characterized by high blood sugar levels due to insufficient insulin production (Type 1 diabetes) or ineffective use of insulin by the body (Type 2 diabetes). Symptoms include increased thirst, frequent urination, weight loss, and fatigue.
These examples highlight the diversity of pathologies and diseases that can affect different organs and organ systems, emphasizing the importance of understanding their specific characteristics, mechanisms, and appropriate management strategies.
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Which one of the following is not a characteristic of impetigo?
a. Can be caused by Staphylococcus aureus
b. Can be caused by Streptococcus pyogenes
c. Can be caused by Pseudomonas
d. Is highly contagious
e. Common in children
Impetigo is a contagious bacterial skin infection characterized by the formation of blisters or sores. While impetigo can be caused by Staphylococcus aureus and Streptococcus pyogenes, it is not typically caused by Pseudomonas. The correct answer is option c.
Staphylococcus aureus and Streptococcus pyogenes are the most common pathogens associated with impetigo. Staphylococcus aureus is responsible for the majority of non-bullous impetigo cases, while Streptococcus pyogenes is commonly associated with bullous impetigo. Pseudomonas, on the other hand, is not considered a common causative agent of impetigo.
Impetigo is highly contagious and can easily spread through direct contact with the infected person or contaminated objects. It is more prevalent in children, primarily due to their close contact with each other in schools and daycare settings. Prompt diagnosis and appropriate treatment are crucial in managing impetigo and preventing its spread.
The correct answer is option c.
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Which of the following are characteristics of lipid? (select all that apply) a.They are non-polar b.They are composed of fatty acids c.they make of membranes d.glycerol is a key component e.They speed up chemical reactions
Lipids are molecules that play a vital role in biological systems. The characteristics are a. They are non-polar b.They are composed of fatty acids c. They make of membranes d. Glycerol is a key component
The following are the characteristics of lipids:
They are non-polar: A lipid molecule is non-polar, meaning it does not have a positive or negative charge. The non-polar nature of lipids makes them water-insoluble and hydrophobic.
They are composed of fatty acids: Lipids are composed of a long chain of hydrocarbon molecules called fatty acids. Lipids can contain one or more fatty acid chains, and the properties of lipids vary depending on the type of fatty acid chains present. For example, saturated fatty acids tend to be solid at room temperature, while unsaturated fatty acids tend to be liquid.
They make up membranes: Lipids are the primary components of cell membranes. Phospholipids, which consist of a glycerol backbone, two fatty acid chains, and a phosphate group, are the most abundant type of lipid in cell membranes.
Glycerol is a key component: Glycerol is a key component of lipids. It forms the backbone of triglycerides, which are the most common type of lipid found in the human body. Triglycerides are composed of three fatty acid chains bonded to a glycerol molecule.
They do not speed up chemical reactions: Unlike enzymes, which are biological molecules that speed up chemical reactions, lipids do not have this capability.
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which of the following karyotypes can represent female drosophilia where an X can represent an X Chromosome. a y represent a y chromosome and an A Represents a state of Autosome.
a. XX AA
b. Xy AA
c. X AA
d. XXy AA
e. two options are correct.
In a female Drosophila, the karyotype that can represent the X chromosome, Y chromosome, and Autosome is XX AA. In other words, the correct option is A.
Karyotypes are pictorial representations of chromosomes that provide information on the number, form, and size of an organism's chromosomes. They are obtained by staining chromosomes in metaphase, a stage of cell division where chromosomes are visible and well-separated.
In Drosophila, karyotypes have 4 chromosomes: 2 sex chromosomes and 2 Autosomes. Females have XX chromosomes, while males have XY chromosomes. Thus, karyotypes in females are represented as XX, and in males, as XY. Autosomes are represented by A, and sex chromosomes are represented by X or Y. Hence, the correct karyotype for a female Drosophila where X represents an X Chromosome, Y represents a Y chromosome, and A represents a state of Autosome is XX AA.
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Application test Scenario 3 – Vaccination
Marcella is 7 months pregnant with her first child. At her most recent antenatal appointment her doctor recommended that she receive a booster of the diphtheria, tetanus, pertussis (DTaP) vaccine. The doctor explained that by having a booster, Marcella will be able to protect her baby during the first 6 weeks of it’s life. This is when whooping cough, the disease caused by infection with the bordetella pertussis bacteria, poses the greatest risk of infant mortality. The doctor also suggested that other people who will be in close contact with the baby within the first 6 weeks, such as Marcella’s partner and the baby’s grandparents, should also have a booster shot.
DTaP boosters for pregnant women are recommended because research has shown that the pertussis or whooping cough vaccine does not provide long lasting immunity. The current pertussis vaccine is an acellular component vaccine; antigens from diphtheria, tetanus toxin and pertussis are combined with an adjuvant and delivered by intramuscular injection. Children receive 5 doses of the DTaP vaccine at 2, 4, 6, 18 months and 4 years of age. This provides protective immunity throughout childhood.
However, there have been a significant number of whooping cough outbreaks in Australia and other parts of the world in recent years that have resulted in the deaths of a number of babies under the age of 6 months. These outbreaks have mostly occurred in populations where vaccination rates have fallen, but they can spread more widely if protective immunity has waned in the general population.
In response to these outbreaks a large research study was conducted in 2016 to assess levels of immunity to pertussis in the population. To do this researchers measured IgG antibody levels specific for pertussis antigens in the serum of previously vaccinated individuals and correlated the level of antibody with the time since the person’s last vaccination. The study found that within one year of vaccination (completing childhood vaccine schedule, or having a booster) efficacy was 80%, but by 4-7 years after vaccination it had fallen to 41%. In teenagers (~10 years post childhood vaccination) this had fallen to >10%. This means that only 10% of teenagers had a level of antibodies in their serum that would provide protective immunity if they were infected with live Bordetella pertussis. Analysis of recent outbreaks showed that teenagers and unimmunised children were the largest infected groups and it was hypothesised that infected teenagers would pose a serious risk to vulnerable infant siblings.
One interesting finding was that adults over 30 who had received the live attenuated pertussis vaccine (prior to the introduction of the acellular vaccine in the 1990’s) showed higher pertussis-specific antibody levels than teenagers.
Based on the results of this and similar studies, in Australia it is now recommended that all teenagers receive a booster DTaP vaccination in Year 7, that all early childcare and health care workers receive boosters every 10 years and that all pregnant women have a booster in their third trimester of pregnancy.
QUESTIONS (20 MARKS)
1. How will Marcella having a booster DTaP vaccine provide protection for her unborn child? In your answer describe Marcella’s immune response to the vaccine and explain in detail how this will be of benefit to her baby (5 marks)
2. Why does the doctor also recommend that Marcella’s partner and the baby’s grandparents have booster shots? 3. Why is the DTaP vaccine delivered as an intramuscular injection? 4. What is the purpose of the adjuvant included in the DTaP vaccine? 5. Why are multiple doses of the DTaP vaccine given during childhood? 6. Explain why new recommendations for increased delivery of DTaP boosters have been made, why are these specific population groups being targeted? 7. Explain the observation that vaccinated individuals over the age of 30 have higher levels of antibodies specific for pertussis antigens than teenagers. What does this tell us about the two different vaccine formulations? 8. Why do you think the live attenuated vaccine is no longer used?
1) Marcella having a booster DTaP vaccine provide protection for her unborn child. 2) Marcella's partner and the baby's grandparents are recommended to have booster shots. 3) The DTaP vaccine is delivered as an intramuscular injection because it allows efficient absorption. 4) The purpose of the adjuvant is to enhance the immune response. 5) Multiple doses of DTaP vaccine ensure the development of long-lasting immunity. 6) New recommendations for increased delivery to combat the waning immunity. 7) The observation suggests a difference in the two vaccine formulations. 8) The live attenuated vaccine is no longer used due to concerns about safety .
Marcella having a booster DTaP vaccine will provide protection for her unborn child through the transfer of maternal antibodies. When Marcella receives the vaccine, her immune system recognizes the antigens from diphtheria, tetanus, and pertussis and mounts an immune response. This response leads to the production of specific antibodies against these pathogens.
Marcella's partner and the baby's grandparents are recommended to have booster shots to create a protective barrier around the baby. By receiving the booster vaccine, they can also develop immunity against diphtheria, tetanus, and pertussis. This reduces the chances of them contracting and transmitting these diseases to the baby, further safeguarding the baby's health.
The DTaP vaccine is delivered as an intramuscular injection because it allows for efficient absorption and uptake of the vaccine components into the bloodstream. Intramuscular injections provide a deeper and more direct delivery into the muscle tissue, facilitating the activation of the immune response.
The purpose of the adjuvant included in the DTaP vaccine is to enhance the immune response. Adjuvants are substances added to vaccines to improve their effectiveness by boosting the body's immune reaction to the vaccine antigens. In the case of the DTaP vaccine, the adjuvant helps to increase the immune response to the diphtheria, tetanus, and pertussis antigens, leading to a stronger and more prolonged immune protection.
Multiple doses of the DTaP vaccine are given during childhood to ensure the development of long-lasting immunity. The initial doses help prime the immune system, while subsequent doses act as booster shots, reinforcing and extending the immune response. By administering multiple doses, the vaccine provides a robust and sustained immunity against diphtheria, tetanus, and pertussis throughout childhood.
New recommendations for increased delivery of DTaP boosters have been made to combat the waning immunity observed in the general population. Studies have shown that the protective efficacy of the pertussis vaccine decreases over time.
The observation that vaccinated individuals over the age of 30 have higher levels of antibodies specific for pertussis antigens than teenagers suggests a difference in the two vaccine formulations. The older individuals received the live attenuated pertussis vaccine, which appears to provide more robust and longer-lasting immune protection compared to the acellular pertussis vaccine given to teenagers.
The live attenuated vaccine is no longer used due to concerns about safety and side effects. While the live vaccine was effective in providing immunity, it carried a small risk of causing the actual disease in rare cases, particularly in individuals with compromised immune systems.
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A client with Cushing's syndrome may manifest signs of diabetes mellitus because: Select one: a. Tissue catabolism results in a negative nitrogen balance b. Glucocorticoids accelerate the process of g
The correct answer is option B: Glucocorticoids accelerate the process of gluconeogenesis, which can lead to an increase in blood sugar levels and insulin resistance, putting people with Cushing's syndrome at a higher risk of developing diabetes mellitus.
A client with Cushing's syndrome may manifest signs of diabetes mellitus because glucocorticoids accelerate the process of gluconeogenesis. Cushing's syndrome is a rare disorder that occurs when the body is exposed to high levels of cortisol for an extended period.
Cortisol is the hormone responsible for regulating blood sugar levels, among other things.
Diabetes is a condition that results in high blood sugar levels due to the body's inability to produce enough insulin or properly utilize insulin. People with Cushing's syndrome may experience an increase in blood sugar levels as a result of high cortisol levels.
Cortisol increases blood sugar levels by promoting gluconeogenesis, a process by which the liver converts fats and proteins into glucose. High levels of cortisol also cause insulin resistance, making it more difficult for the body to use insulin effectively.
As a result, people with Cushing's syndrome are at a higher risk of developing diabetes mellitus.
Cushing's syndrome can also cause muscle wasting and tissue catabolism, which can result in a negative nitrogen balance.
However, this is not directly related to the development of diabetes mellitus.
Therefore, the correct answer is option B: Glucocorticoids accelerate the process of gluconeogenesis, which can lead to an increase in blood sugar levels and insulin resistance, putting people with Cushing's syndrome at a higher risk of developing diabetes mellitus.
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If the genotype frequency of a population at one time is 25+.50+25 and when measured 40 years later it is.16+.48+.36 then evolution _____happening.
If the genotype frequency of a population at one time is 25+.50+25 and when measured 40 years later it is.16+.48+.36 then evolution is happening.
The process of change over time is referred to as evolution. It may be physical changes among an organism's populations over many generations. Evolution is the change in genetic structure of a population over time due to the frequency of alleles. The genotype frequency of a population at one time is 25+.50+25 and when measured 40 years later it is.16+.48+.36, therefore evolution is happening. The frequency of a population genotype can change over time due to evolution. The given data implies that the population's genotype frequency has shifted after 40 years, thus it is undergoing evolution.
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For SARS-CoV-2 (COVID-19) answer the following questions: How is
it most likely transmitted person to person? What receptor does the
Spike protein bind to and list the 3 cell types with the highest
ex
The Spike protein of SARS-CoV-2 (COVID-19) binds to ACE2 receptors on human cells. This allows the virus to enter the cells and replicate, leading to the transmission of the disease.
ACE2 is a protein found on the surface of certain cells in the human body, particularly in the respiratory system. The spike protein of the virus interacts with ACE2 to facilitate its entry into the host cell.
The binding process involves specific interactions between certain regions of the spike protein and the ACE2 receptor. The receptor-binding domain (RBD) of the spike protein is responsible for recognizing and attaching to the ACE2 receptor. This interaction is essential for the virus to enter and infect host cells.
The spike protein undergoes a conformational change when it interacts with ACE2, allowing the virus to fuse with the host cell membrane and release its genetic material into the cell. This initiates the process of viral replication and the production of new virus particles.
Understanding the interaction between the spike protein and ACE2 is crucial in developing strategies to prevent viral entry and develop effective treatments or vaccines against COVID-19.
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After making an oligopeptide, you thought you would also try making a polynucleotide. (Why not? You are a mad scientist after all!) Write out the DNA sequence using the following instructions (5 marks): • This is a double stranded DNA hydrogen bonding with each other following the principle of complementary base-pairing Each strand contains ten nucleotides Each strand contains all four different types of nucleotides You should indicate clearly the directionality of each strand in your answer You do not need to draw the full nucleotide structure. Use the one-letter code (A, T, G, C, or U) to represent each nucleotide 2) After making an oligopeptide, you thought you would also try making a polynucleotide. (Why not? You are a mad scientist after all!) Write out the DNA sequence using the following instructions (5 marks): • This is a double stranded DNA hydrogen bonding with each other following the principle of complementary base-pairing Each strand contains ten nucleotides Each strand contains all four different types of nucleotides You should indicate clearly the directionality of each strand in your answer You do not need to draw the full nucleotide structure. Use the one-letter code (A, T, G, C, or U) to represent each nucleotide
The given outline shows up a 10-nucleotide double-stranded DNA sequence with complementary base-pairing, illustrating the directionality and nucleotide composition of each strand.
How to write out the DNA sequence
Based on the given information, here is a case of a double-stranded DNA sequence:
5'-ATCGCTAGCG-3' (sense strand, examines from cleared out to right)
3'-TAGCGATCGC-5' (antisense strand, examines from right to clear out)
In this sequence, both strands are complementary to each other, and each strand contains ten nucleotides. The sense closes with guanine (G) and starts with adenine (A), while the antisense strand starts with thymine (T) and closes with cytosine (C).
On the off chance that you do not intellect note that DNA courses of action can move broadly, and the given gathering is reasonable an outline that meets the given criteria. The genuine gathering can shift in terms of nucleotide composition and course of activity.
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