You want to know the exact location of a protein inside the cell. You know the gene sequence of the protein. There are antibodies available for this protein. Describe any one method you can use to visualize this protein.

Answers

Answer 1

Answer: Western Blotting

Explanation:

The sample is first denatured followed by the gel electrophoresis. Animal derived or synthetic antibody is produced which has the ability to bind to the protein.

The electrophoresis membrane is then washed by primary antibody before the excess antibody is washed off.

Then the secondary antibody is added to get attached to the primary antibody and then it can be visualized by immunofluorescence or some other method.

Answer 2

Answer:

Fluorescent Staining Method

Explanation:

Fluorescent staining uniformly stains protein, is rapid and offers sensitivity equal to that attained by silver staining method. It involves no destaining step and is compatible with mass spectrometry and microsequencing. Commercially fluorescent stains are available to stain 1D or 2D gels to visualize bands.


Related Questions

In fruit flies, long wings (W) are dominant over short wings (w), and brown pigments (N) are dominant over yellow pigments (n). Each individual possesses two alleles for each trait.
1. If a fly that is homozygous dominant for both traits is crossed with a fly that is homozygous recessive for both traits, what is the predicted genotype of the offspring?

Answers

Answer:

WwNn

Explanation:

Long wings (W) are dominant over short wings (w)Brown pigments (N) are dominant over yellow pigments (n)

A fly that is homozygous dominant for both traits (WWNN) is crossed with a fly that is homozygous recessive for both traits (wwnn).

All gametes produced by the WWNN individual will be WN, and all gametes produced by the homozygous recessive individual will be wn.

When the gametes from the two parents combine, the zygote will be heterozygous for both genes, with the genotype WwNn.

Final answer:

The offspring from a homozygous dominant fruit fly (WWNN) and a homozygous recessive fly (wwnn) will all have the heterozygous genotype WwNn, displaying long wings and brown pigments.

Explanation:

In classical Mendelian genetics, long wings (W) are dominant over short wings (w), and brown pigments (N) are dominant over yellow pigments (n). When a homozygous dominant fruit fly for both traits (WWNN) is crossed with a homozygous recessive fly (wwnn), the resulting genotypes for all the offspring will be heterozygous for both traits (WwNn), expressing the dominant phenotypes—long wings and brown pigments.

The scenario is straightforward as both traits are being considered separately, and the inheritance pattern follows simple Mendelian inheritance, not taking into account potential linkage or sex linkage as in X-linked crosses. Therefore, all offspring produced from this cross will have the same genotype, with one dominant and one recessive allele for each gene, showcasing the principle of uniformity in the F1 generation.

Starting with a single cell, how long (in hours) will it take for the mass of an E. coli culture to equal that of the Earth? Assume exponential phase and limitless nutrients.

Answers

Answer:

43.6 hours, which is less than two days.

Explanation:

To calculate Growth for an exponentially growing populations

Nt = N▪ * 2^n

Where,

N▪= cell number at initial time

Nt = cell number at later time

n = number of generations

Assuming exponential phase and limitless nutrients

How long until E.coli conquers the earth?

Given,

1 doubling = 20 min = 0.33hr

N▪= Mass = 9.5 x 10^-13 g/bacterium

Nt= Mass = 5.9 x 10^27 g/Earth

Nt = N▪ * 2^n

5.9 x 10^27 = 9.5 x 10^-13 * 2^N

nlog(5.9 x 10^27) = log(9.5 x 10^-13) + nlog(2)

27.7 = -12.0 + n(0.3)

27.7 + 12.0 = n(0.3)

39.7 = n(0.3)

132 = n

Therefore,

132 generations * 0.33 hour/generation = 43.6 hours

43.6 hours is less than two days.

Our answer for a single cell, it will take less than two days for the mass of an E. coli culture to equal that of the Earth on assuming exponential phase and limitless nutrients.

A species of beetle expresses a pigment protein as an adult but not as a juvenile. The pigment is encoded by the gene PIG. A protein called KID, which is only present in juveniles, is a transcription factor that binds to the DNA near the protein-coding sequence for PIG. Do you think KID is a negative regulator of PIG or a positive regulator? Why?

Some individuals in the species never express the pigment (neither as a juvenile or as an adult). Do you think they have a mutation in the KID gene, the KID binding site, or in the protein-coding part of the PIG gene? Why? (the ‘why’ part of the question will only be used to help us give possible credit for answers different than what we think is the clearest answer)

Answers

Answer:

The KID protein is responsible for the no pigmentation at the juvenile stage. When the KID protein inhibits in the adult state, the pigmentation occurs in the body. This might occur because the KID protein acts as the repressor molecule and acts as a negative regulator of PIG protein.

The KID protein is responsible for pigmentation an adult stage.  Any mutation in the KID gene might result in the loss of pigmentation in the adult. The KID gene is responsible for the binding of the KID protein and mutation in this gene can lead to the arrest of KID protein. The protein is unable to release and PIG continuously repressed in the adults.

Explain why evolutionary biologists monitor selec- tively neutral polymorphisms as molecular clocks.

Answers

Answer:

Because of their property of preciseness and rhythmic repetitions like a normal clock sequence...

Explanation:

Evolutionary biologist use these neutral polymorphisms as molecular clock because of their gradual accumulation of  mutations that remain on changing gradually in a uniform sequence overlarge number of generations. These changing sequences are highly precise over and over, that's why these are also termed as neutral mutations.

Select the true statements about protein secondary structure. a. The α‑helix is held together by hydrogen bonds between the amide N − H N−H and C = O C=O groups. b. In a β‑pleated sheet, the side chains are located between adjacent segments. c. In an α‑helix, the side chains are located on the outside of the helix. d. The secondary level of protein structure refers to the spatial arrangements of short segments of the protein. e. Peptide bonds stabilize secondary structure.

Answers

Answer:.

→The α‑helix is held together by hydrogen bonds between the amide N − H N−H and C = O C=O groups

→ In a β‑pleated sheet, the side chains are located between adjacent segments.

→ In an α‑helix, the side chains are located on the outside of the helix. .

→ The secondary level of protein structure refers to the spatial arrangements of short segments of the protein

Explanation:

This is the level of protein which  results from spatial arrangement  produced by the formation of hydrogen bonds between the  oxygen atom  of one carboxyl group(c=0) group, and hydrogen of the NH group of  amino acids  four places ahead of it .( The resulting structure is  coiled and are therefore called alpha-helices)

AND  

Hydrogen bonds  between adjacent amino acids that  join them side by side  so that the  bonds appear straight rather than coil, and the chains form upwards-downwards-upward- downwards format to form flat shaped structure called beta-pleated sheet.  

The hydrogen  bonding is due to strong polarities of the –NH- CO- groups of amino acids.

The two structures account for the spatial arrangement of secondary protein structure. Secondary structure is stabilized by the orientation and aggregation of these hydrogen bonds. . The outwards distributions of the side chains, the non-polar nature (hydrophobic) of   alpha-helix makes  some secondary proteins ideal as integral  membrane proteins.

 Note- peptide bond stabilizes primary protein structure.

The following statements are true for protein secondary structure:

The amide N-H and C=O groups form hydrogen bonds that hold the -helix together.In a helix, the side chains are found outside the helix.The secondary structure is stabilized by peptide bonds.

Therefore, the correct options are A, C and E.

The polypeptide chain is regularly coiled to form a -helix, and hydrogen bonds between the amide NH and C=O groups help to stabilize the structure. Because they occur outside the helix and extend outward in a -helix, amino acid side chains enable interactions with the environment. The covalent bonds that link amino acids together, known as peptides, are essential for maintaining the secondary structure. Rotation is hindered by the planar structure of the peptide bond, which helps to form regular patterns such as the -helix.

Therefore, the correct options are A, C and E.

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1. If the frequency of two alleles in a gene pool is 90% A and 10% a, what is the frequency of individuals in the population with the genotype Aa?

Answers

Answer: 0.18

Explanation:

For the alleles, the percentage distribution of each is 'A' (90% = 0.9)

While 'a' (10% = 0.1)

Hence, 0.9 and 0.1 are the respective frequencies of each allele

Now, apply Hardy-Weinberg Equilibrium equation, where heterozygotes are represented by the 2pq term.

Therefore, the number of heterozygous individuals (Aa) is equal to 2pq which equals

2 × 0.9 × 0.1 = 0.18

Thus, the frequency of heterozygote is 0.18, while the percentage distribution in the population is 18%

Addition of ________causes the induction of the ______________ polymerase. This polymerase then binds to the T7 ________________ upstream of the rGFP gene, resulting in the _____________________ of rGFP gene to produce rGFP mRNA. This mRNA is then ______________________ to produce the rGFP protein .

Answers

Answer:

Addition of HEAT causes the induction of the T7 RNA polymerase. This polymerase then binds to the T7 RNA POLYMERASE PROMOTER upstream of the rGFP gene, resulting in the TRANSCRIPTION of rGFP gene to produce rGFP mRNA. This mRNA is then TRANSLATED to produce the rGFP protein

Explanation:

T7 RNA polymerase is a warmth inducible compound that is initiated inside the nearness of a warmth source. This polymerase ties to a chose grouping alluded to as the T7 RNA Polymerase advertiser succession. It moves along the DNA grouping prompting the amalgamation of mRNA during a procedure alluded to as translation.  

This mRNA is changed over into a protein item through a procedure alluded to as interpretation.

List the sources of experimental uncertainty. List steps you will take to minimize the uncertainties.

Answers

Answer:

Sources of experimental uncertainties

1. Environment- change in environment can bring about experimental error e.g change Temperature can affect crop yield.

2. Wrong caibration of equipment- some equipment need to be calibrated before use. Wrong calibration brings error

Explanation: steps to uncertainties

1.Calibrate equipment when necessary.

2. Ensure fomulars are rightly imputed for electronic devices

3. Experience and competency is needed to avoid Esperanza uncertainties. Expert can be employed

4. Replication for field work reduces uncertainties. E.g maize of the same varieties can be planted in three places on the field to avoid uncertainties.

Unconditioned negative reinforcers must be related to our inherited capacity to respond to them (for example, aversive, painful stimuli), and conditioned negative reinforcers must be stimuli that were originally neutral events that acquired their effects through previous pairing with existing negative reinforcers.
O True
O False

Answers

Answer: False

Explanation:

Negative reinforcers strengthen a behavior that avoids or removes a negative outcome.

Negative reinforcers are stimuli factors that influence behavior because individuals have capacity we inherited to respond to them and  effects of these reinforcers have been established through records and histories of learning. Negative reinforcers are at the mercy of type of response acquired. Negative reinforcers are sources of negative reinforcements.

Unconditioned negative reinforcers

stimuli is one whose removal strengthens the choice behavior in absence of prior learning. Example includes the place of shock, loud noise, intense light.

Other times pain will occasion behavior and other response that eliminates discomfort will be reinforced.

Final answer:

True, unconditioned negative reinforcers are connected to our inherent responses to stimuli like pain, whereas conditioned negative reinforcers are learned through association with existing negative reinforcers. In operant conditioning, negative reinforcement increases the likelihood of a behavior's occurrence by removing an unpleasant stimulus after the behavior happens.

Explanation:

True, unconditioned negative reinforcers are related to our inherent responses to stimuli such as pain, and these unconditioned responses do not require learning. On the other hand, conditioned negative reinforcers are originally neutral but become effective through association with existing negative reinforcers. Consider the scratch response to an itchy bug bite: scratching (the response) leads to the removal of the itch (the aversive stimulus), thus negatively reinforcing the behavior of scratching. Punishment, however, whether positive (adding an undesirable stimulus) or negative (removing a desirable stimulus), always serves to decrease a behavior.

Operant conditioning is the learning process through which the strength of a behavior is modified by reinforcement or punishment. B.F. Skinner, a renowned psychologist, distinguished between reinforcement and punishment, and further between the positive and negative forms of these phenomena. A stimulus that serves as a negative reinforcer for someone may not serve the same function for another, highlighting the subjectivity of these responses.

28. Select all accurate statements
A. All chordates will have a muscular post an*l tail
B. All chordates have a dorsal, hollow nerve cord.
C. All chordates have pharyngeal slits or clefts
D. All chordates will have a notochord in their development and/or adulthood
E. All chordates are bilaterally symmetrical animals

Answers

Answer:

its A but I am not sure I just tried

Answer:

All the options A,B,C,D and E are correct.

Chordates possess a muscular posterior tail, a dorsal, hollow nerve cord, pharyngeal slits or clefts, a notochord in their adulthood and are bilaterally symmetrical animals.

True or False, it's likely that organisms other than LUCA existed alongside LUCA before the divergence of bacteria from archaea and eukaryotes.

Answers

Answer:

False

Explanation:

Which of the following is/are true?
A. The fungal pathogen Mycosphaerealla graminicola is found worldwide with its host, cultivated wheat. Mycopharealla graminicola is host specific and does not occur on other host species such as Barley.
The closest known relative of M. graminicola is a barely-adopted pathogen Septoria passerinii.
You are researching these fungi and have the following hypothesis: If M. graminicola and 5 passerinii both had a common ancestor that lived in one geographic area where wheat and barley grew, it may be possible that the ancestor gave rise to these two species in one geographic location. This would be classified as sympatric speciation.
Your hypothesis and definition of sympatric speciation is correct.
B. A flood causes the loss of all red-headed males ducks in a population. This is an example of sympatric speciation.
C. A plant species obtain an extra set of homologous chromosomes. This would be an example of sympatric speciation.
D. Sympatric speciation may be due to sexual (mate) selection.
E. Sympatric speciation can occur when a single species occupies the same geographic location.

Answers

Answer: Option C, D, E and A

Explanation:

Sympatric speciation is the evolution or isolation of new species from the original population of species occupying the same geographic area. It is also due to sexual selection of mates leading to reproductive barriers. A plant with extra set of homologous chromosomes is an example. Sympatric speciation is due to isolation of new species from the population of species who arise from common anscetor.

The presence of an oceanic trench, a chain of volcanic mountains along the edge of a continent and deep seated earthquakes is characteristics of ___?

Answers

Answer:

ocean-continent plate convergence

Explanation:

The presence of an oceanic trench, a chain of volcanic mountains along the edge of a continent and deep seated earthquakes is characteristics of ocean-continent plate convergence

Hope this help

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Final answer:

The presence of an oceanic trench, a chain of volcanic mountains along the edge of a continent and deep-seated earthquakes is characteristic of a convergent plate boundary, which typically forms when an oceanic plate is subducted under a continental plate.

Explanation:

The presence of an oceanic trench, a chain of volcanic mountains along the edge of a continent, and deep-seated earthquakes, are indications of a convergent plate boundary. This typically happens when an oceanic plate is subducted or pushed beneath a continental plate, forming a deep oceanic trench. The intense heat and pressure cause the subducted plate to partially melt, and this molten material can rise to form a chain of volcanic mountains along the edge of the continent, often known as a volcanic arc. The process of subduction also leads to seismic activity or earthquakes that are deep-seated.

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Sickle cell anemia and albinism are both recessive traits in humans. Imagine that a couple, already pregnant with twins, has just learned that they are both heterozygous for both of these traits.As the couple's genetic counselor, the couple asks you the following questions about how their carrier status will affect their offspring.Part AIf the couple has fraternal twins, what is the probability that both children will be unaffected by both conditions?Part BIf the couple has fraternal twins, what is the probability that both of the couple's children will have both sickle cell anemia and albinism?Part CWhat is the probability that one of the fraternal twins is a carrier of either, but not both, of the conditions?(Hint: You will need to use both the product law and the sum law to answer this question.)Part DIf the couple has fraternal twins, what is the probability of having two phenotypically normal children, one being a carrier of only the sickle cell anemia recessive allele, and the other being a carrier of only the recessive allele for albinism?(Hint: You will need to use both the product law and the sum law to answer this question.)

Answers

A. 81/256  B.1/256 C 4/9     D 1/4

Explanation:

A. Both the parents are heterozygous for sickle cell anaemia, the probability of gene passing to one child is

1/2A*1/2= 1/4 A

The probability of albinism in one of the child of heterozygous parents:

1/2*1/2= 1/4 A

Now from the above data the probability of a child not having albinism the diseases will be known by:

1-1/4 A

= 3/4 A

Similarly for sickle cell anemia the probability of not occurring the disease is also 3/4 S

Now applying the product rule for getting the probability of both the diseases not occurring.

3/4 A*3/4 S = 9/16

Here the two fraternal twins are in question, so the probability of both the children to be unaffected will be 9/16*9/16

=81/256

B. The chances for each child to inherit defective gene from each parent in case of Albinism .is A 1/2*1/2  = 1/4 A

Similarly same with sickle cell anaemia

1/4 S

applying the product law, we can determine the probability of the occurrence of both the diseases in one child

1/4*1/4

1/16

Hence in two children that are fraternal twins, the probability is

1/16*1/16

= 1/256

C. From the data, we can see that  the probability of twin to be a carrier is 2/3

the chance of occurrence of both the diseases in one child is

2/3*2/3

=4/9

The chances of not carrying the gene of either disease is1/3*1/3

=1/9

Thus, we can know the probability that if it happens to be fraternal twins the chances of diseases

1-4/9+1/9

=4/9

D. we know that the probability of one fraternal twin carrying a gene for either disease:

chances of carrying the gene is 3/4

chances of not occurrence of gene 1/3

So, in case of fraternal twins 3/4*3/4= 9/16

                                               1/3*1/3 = 1/9

So,1- 9/16+1/9

    = 1/4

Angela wants to start a company developing apps. She needs access to R&D to be able to use the newest technologies. Of the conditions that need to be put in place for the Entrepreneurial Ecosystem, she needs ______

Answers

Answer:

Research and Development Transfer

Explanation:

she needs Research and Development Transfer, which involves the transferring of technology/skills from the individual or company that owns or holds it to another individual or company.

You plan to expose your chlamydomonas culture to 100 nM colchicine to inhibit new protein synthesis. You need to treat 1 x 108cells. The density of your culture is 5 x 107 cells/ml. The molecular weight of colchicine is 399.44. Explain what you need to do. Show your calculations.

Answers

Answer:

mass(g) of colchicine = 3.99 × 10⁻⁵g

Explanation:

Given that;

the number of moles colchicine =  100 nM = 100 × 10⁻⁹M

Density of chlamydomonas culture = 5 × 10⁷ cells/mL

∴ In 1mL of chlamydomonas culture there are 5 × 10⁷ cells present.

To decide the number of one cell, we need to use [tex]\frac{1}{5*10^7}[/tex] mL of the cellulose

However, 1 × 10⁸ cells will be present in [tex]1*10^8*\frac{1}{5*10^7}[/tex] mL , which in turn give us;

[tex]\frac{10^8}{5*10^7}[/tex]mL

Afterwards, to get the required 1 × 10⁸ cells, 2mL(molarity, since molarity=  no of moles/litre) has to be taken

If colchicine has to be treated, we need to determine the mass of colchicine that is required in the process as well;

since,  the number of moles colchicine =  100 nM = 100 × 10⁻⁹M

And, the given molecular weight = 399.44;

we can determine the mass of colchicine as;

∴ [tex]numberofmoles = \frac{mass(g)}{molar mass(g)}[/tex]

substituting the parameters given, we have:

[tex]100*10^{-9}= \frac{mass(g)}{399.4}[/tex]

mass(g) = 399.4 × 100 × 10⁻⁹

            = 3.99 × 10⁻⁵g

Hence, the mass of colchicine that is required in the process to make 100 nM dissolve in the in 2mL of the culture in one Litre of water  is 3.99 × 10⁻⁵g.

Was the rate of increase of sucrase activity greater when sucrose concentration went from 2.5 to 7.5 g/l or when it went from 22.5 to 27.5 g/l?

Answers

Answer: It is greater when sucrose concentration went from 2.5 to 7.5g/l.

Explanation: The rate of reaction of an enzyme is known to be affected by the rate of concentration of its substrate, which in this case is the sucrose Solution.

If the rate of increase of concentration is high,the activities of the enzyme SUCRASE will increase accordingly, in order to breakdown the substrate.

The rate of increase of Sucrose from 2.5 to 7.5g/l is higher(300%) than the rate of Increase of Sucrose from 22.5 to 27.5g/l (1.22%). It is expected under circumstances that the action of SUCRASE will increase at a rate higher in the first Solution than in the second Solution.

Final answer:

The rate of increase in sucrase activity depends on the concentration of sucrose and whether or not the enzyme is saturated. The increase could be greater at lower concentrations (2.5 to 7.5 g/l) if sucrase is not yet saturated. The increase might be less at higher concentrations (22.5 to 27.5 g/l) if sucrase is near or at saturation point.

Explanation:

The increase in sucrase activity is generally considered to be a response to the concentration of substrate present, in this case, sucrose. The increase in activity happens because more substrate (sucrose) is available for the enzyme (sucrase) to act upon. However, there is a limit to this increase. Once the enzyme is saturated with substrate, further increases in substrate concentration do not increase the enzyme's activity. This is known as the saturation point.

To determine whether sucrase activity increased more when sucrose concentration increased from 2.5 to 7.5 g/l or from 22.5 to 27.5 g/l, we would need specific data on the rate of sucrase activity at these different concentrations. It's possible that the increase from 2.5 to 7.5 g/l was greater if this is in the ascending portion of the enzyme activity curve and the sucrase was not yet saturated with sucrose. Conversely, the increase from 22.5 to 27.5 could be lesser if the sucrase is near or at saturation point.

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Using the principles of natural selection, __________ studies how behavior and the mind have evolved.

Answers

Answer:

Evolutionary psychology

Explanation:

Evolutionary psychology is the theoretical branch of psychology that describes that how the human behavior have evolved by the effect of evolution through a lens

Only body is not effected by evolution but the brain is also sculpted; the behavior it produce and psychological procedure.There were many psychological mechanisms that were involved in survival of species known as psychological adaptation.The psychological adaptations and their byproducts that are activated in modern environment are different from their ancestral environment in some features.

Example;

Our brain insructs us to behave in an adaptive way.

Based on the definition of a watershed, how many different watersheds were there in your model? Explain how you determined this number.

Answers

Answer:

Water shed is created when an area or land separates the water flowing to different rivers, basin and seas.

Explanation:

Water shed are of different types-

Large water sheds-Contain well developed channel networks.Small water sheds-Contain dominant land phase.Urban watershed-It is dominated by building,roads,pavements.Agriculture water shed-Forest water shed-Evapotranspiration is the dominant component of the hydrologic cycle.Mountain water shed-mountain is the dominant component that separates the water flow.Desert water shed-Sand dunes sand mounds that are formed by blowing air causes separation of water flow.Coastal watershed-Coastal area may partly be urban and is dynamic contact with sea.The hydrology is influenced by tidal action.
Final answer:

The number of watersheds in a model depends on its design. Watersheds are areas of land that drain into common outlets, such as a reservoir or bay. To determine how many watersheds are in a model, identify the common outlets and each individual area that drains into one of these outlets is a separate watershed.

Explanation:

The number of watersheds in your model depends on how your model is designed. A watershed is an area of land that drains all the streams and rainfall into a common outlet such as the outflow of a reservoir, mouth of a bay, or any point along a stream channel.

To determine the number of watersheds in your model, you need to identify the points at which water flows together, and designate those as common outlets. Each individual area that drains into one of these common outlets comprises a separate watershed. For example, if your model includes three rivers which all converge at a single point, you would have three watersheds.

This definition also implies that all of the land on earth can be divided into watersheds. The boundaries of a watershed are determined by the topography (i.e., the hills and valleys) that guides the direction of water flow.

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Which of the following is/are true?
A. Sympatric speciation most commonly occurs due to sexual (mate) selection.
B. Sympatric speciation can only occur when a single species occupies the same geographic location.
C. A plant species obtain an extra set of homologous chromosomes. This would be an example of sympatric speciation.
D. A flood causes the loss of all red-headed males ducks in a population. As a result, the red-headed female ducks must breed with yellow-headed male ducks, which are not their preferred mates. This is an example of sympatric speciation.
E. The fungal pathogen Mycosphaerella graminicola is found worldwide with its host, cultivated wheat. Mycosphaerella graminicola is host specific and does not occur on other host species such as Barley.
The closest known relative of M. graminicola is a barely-adapted pathogen Septoria passerinii.
You are researching these fungi and have the following hypothesis: If M. graminicola and S passerinii do not have a common ancestor that lived in one geographic area where wheat and barley grew, it may be possible that a common ancestor gave rise to these two species. This would be classified as sympatric speciation.
Your hypothesis and definition of sympatric speciation is logical.

Answers

Answer: A, C, and E are correct

Explanation:

Sympatric speciation is a random or naturally occurring event whereby organisms of the same species:

- live in the same territory or nearby territories ( i.e no single specie occupy

an area in isolation)

- DO NOT interbreed, but select a sexual mate from a much diverse territory and practice non-random mating, which favors some genes results in an uneven gene flow or disruption of alleles previously common among the population.

- produce offspring with extra sets of chromosomes known as polyploidy, leading to show genetic variations

Finally, M. graminicola and S passerinii are Sympatric species based on the already given explanation.

Suppose two parents, a father with the genotype AaBbCcDdee and a mother with the genotype aabbCcDDEe, want to have children. Assume each locus follows Mendelian inheritance patterns for dominance. What proportion of the offspring will have each of the specified characteristics?

Answers

Answer:

A. same genotype as the father (AaBbCcDdee) = (½ x ½ x ½ x ½ x ½) = 0.03

B. phenotypically resemble the father (A_B_C_D_ee) = (½ x ½ x ¾ x 1 x ½) = 0.09

C. same genotype as the mother (aabbCcDDEe) = (½ x ½ x ½ x ½ x ½) = 0.03

D. phenotypically resemble the mother (aabbC_D_E_) = (½ x ½ x ¾ x 1 x ½) = 0.09

E. phenotypically resemble neither parent (simply subtract the probability of phenotypically resembling each parent from 1) = 1 – (0.09375 + 0.09375) = 0.81

Explanation:

The computation of the total probability would simply be the product of individual chances for each particular gene.

This can be better gotten with the punnette sqaure

The study of genes and inheritance is called genetics.

The correct answer is 0.81

What are genes?The structural and functional unit of the DNA is genes and able to code the sequence of the DNA.

The answer is as follows:-

Same genotype as the father (AaBbCcDdee) =[tex]\frac{1}{2} *\frac{1}{2} *\frac{1}{2} *\frac{1}{2} *\frac{1}{2} [/tex] = 0.03Phenotypically resemble the father (A_B_C_D_ee) = [tex]\frac{1}{2}*\frac{1}{2}*1*\frac{3}{4}*\frac{1}{2} = 0.09[/tex]Same genotype as the mother (aabbCcDDEe) = [tex]\frac{1}{2} *\frac{1}{2} *\frac{1}{2} *\frac{1}{2} *\frac{1}{2} [/tex]= 0.03phenotypically resemble the mother (aabbC_D_E_) =[tex]\frac{1}{2}*\frac{1}{2}* \frac{3}{4} *1*\frac{1}{2} = 0.09[/tex]

Phenotypically resemble neither parent (simply subtract the probability of phenotypically resembling each parent from 1)[tex] = 1 - (0.09375 + 0.09375) = 0.81[/tex]

Hence, the correct answer is 0.81

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Crenation and hemolysis A cell placed in a hypertonic solution will shrink in a process called crenation. A cell placed in a hypotonic solution will swell in a process called hemolysis. To prevent crenation or hemolysis, a cell must be placed in an isotonic solution such as 0.9% (m/v) NaCl or 5.0% (m/v) glucose. This does not mean that a cell has a 5.0% (m/v) glucose concentration; it just means that 5.0% (m/v) glucose will exert the same osmotic pressure as the solution inside the cell, which contains several different solutes. Part D

Answers

Question options:

A red blood cell is placed into each of the following solutions. Indicate whether crenation, hemolysis, or neither will occur.

Solution A: 3.21% (m/v) NaCl

Solution B: 1.65% (m/v) glucose

Solution C: distilled H2O

Solution D: 6.97% (m/v) glucose

Solution E: 5.0% (m/v) glucose and 0.9%(m/v) NaCl

Answer:

Crenation: A, D, E

Hemolysis: B, C

Explanation:

Crenation is an osmotic process in which blood cells shrink while placing hypertonic or alkaline solutions.

Crention caused by these hypertonic solutions.

A: 3.21% (m/v) NaCl  (more solutes)  

D: 6.97% (m/v) glucose (more solutes)

D:  5.0% (m/v) glucose and 0.9%(m/v) NaCl  (more solutes)

Hemolysis is the destruction of red blood cells in which cells bloat up and may explode while placing in a hypotonic solution.

Hemolysis caused by these hypotonic solutions.

B: 1.65% (m/v) glucose

C: distilled H2O

Final answer:

Crenation (cell shrinkage) occurs when cells are placed in hypertonic solutions, while hemolysis (cell swelling) occurs when they are put in hypotonic solutions. To maintain cell size and form, cells should be in isotonic solutions, which have the same solute concentration as the cells. Examples of isotonic solutions are 0.9% m/v NaCl or 5.0% m/v glucose.

Explanation:

Crenation and hemolysis are processes that pertain to the behavior of cells in different types of solutions. When a cell is placed in a hypertonic solution - a solution with a greater concentration of solutes compared to the cell's cytoplasm - the water molecules inside the cell will move outside to balance the solute concentration, causing the cell to shrink. This process is known as creation.

On the other hand, if a cell is placed in a hypotonic solution - a solution with a lower solute concentration than the cell's cytoplasm - the water molecules will move into the cell, causing it to swell and potentially burst in a process called hemolysis.

To prevent either crenation or hemolysis from occurring, the cell should be placed in an isotonic solution. An isotonic solution has the same solute concentration as the cell's cytoplasm, ensuring equal water movement in and out of the cell, and thus, maintaining the cell's size and shape. Examples of isotonic solutions are 0.9% (m/v) NaCl or 5.0% (m/v) glucose. However, these percentages do not imply that a cell has a 5.0% (m/v) glucose concentration. It means that these solutions exert the same osmotic pressure as that inside the cell, which has multiple solutes.

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Four of the five factors below support the mechanism of natural selection. In contrast, the fifth factor blocks natural selection from occurring. Which one of the factors listed below does NOT lead to natural selection, but instead blocks it from occurring?

a. Characteristics are inherited passed from parent to offspring.

b. Organisms in a population are identical to each other.

c. There is competition among organisms in a population.

d. More offspring are born than can survive.

e. Organisms in a population vary in characteristics that affect how well they survive and reproduce.

Answers

Answer:

Four of the five factors below support the mechanism of natural selection. In contrast, the fifth factor blocks natural selection from occurring. Which one of the factors listed below does NOT lead to natural selection, but instead blocks it from occurring

Organisms in a population are identical to each other

Explanation:

If organisms are identical then all of them should be able to survive harsh condition but since not all organisms has this identity it makes the law of natural selection not to be supported by the claim. The best organism that thrives survives and pass such trait to the next generation of offspring

Many properties of living things involve the transfer and transformation of energy and matter. For example, plant chloroplasts convert energy from sunlight to what forms of energy or matter?

Answers

Answer:all of

Explanation:

In the 1960s, a population of squirrels was being studied in Alabama and the coat color of the squirrels was found to range from the more common gray color (dominant) to the less common red color (recessive). When they sampled an area, they found 536 gray squirrels and 64 red squirrels. Assuming the population is at Hardy Weinberg's equilibrium, answer the following questions:1. What is the frequency of the homozygous recessive individuals?

Answers

Answer: Assuming the population is at Hardy Weinberg's equilibrium, the frequency of the homozygous recessive individuals is 0.107

Explanation: Hardy-Weinberg law provides an equation to relate genotype frequencies and allele frequencies in a randomly mating population. p² + 2pq + q² = 1 where p² = homozygous dominant, q² = homozygous recessive and 2pq = heterozygous.

Also, for two alleles, p and q, p + q = 1

Using these equations and the information provided in the question given, the total number of squirrels is 600.

Grey squirrels frequency, p² = 536/600 = 0.893

Red squirrels frequency, q² = 64/600 = 0.107

Therefore, the frequency of recessive individuals (Red) = 0.107

Final answer:

The frequency of the homozygous recessive individuals in the squirrel population, assuming Hardy-Weinberg equilibrium, is 10.67%, calculated by dividing the number of red squirrels by the total population.

Explanation:

To determine the frequency of the homozygous recessive individuals in a squirrel population, we can use the Hardy-Weinberg equation. In this case, the recessive phenotype is represented by the red squirrel coloration. We are given that there are 64 red squirrels, which are the homozygous recessive individuals (rr), out of a total of 600 squirrels. The frequency is the number of homozygous recessive individuals divided by the total population.

Since the population is at Hardy-Weinberg equilibrium, we know that the sum of the genotype frequencies (p² + 2pq + q²) equals 1. In this context, 'p' represents the dominant allele frequency, and 'q' represents the recessive allele frequency. The frequency of the homozygous recessive individuals (q²) equals the number of red squirrels (recessive phenotype) divided by the total population.

Therefore, the frequency of the homozygous recessive squirrels is:

q² = 64 red squirrels / 600 total squirrels = 0.1067 (or 10.67%)

This value represents the frequency of the homozygous recessive individuals in the squirrel population.

Primary ciliary dyskinesia (PCD) is a rare genetic disease. Affected individuals exhibit impaired functioning of ciliated cells.
Based on what you know about the role of cilia in eukaryotic cells, why would you expect people with PCD to be particularly susceptible to respiratory infections?

Answers

Answer:

Cilia are motile in the lungs responsible for keeping the airways clear of dirt and mucus by their characteristic beating motion and rhythmic waving allowing a person to breathe easily and without irritation. These are present in both the lungs as well as middle ear.

As in Primary ciliary dyskinesia , there are defects in the action of cilia in the lining of the respiratory tract , middle ear , sinuses , eustachian tube etc the cilia cannot peforms its regular role .Infections can lead to an irreversible scarring and obstruction in the bronchi resulting in :

1) Shortness of breath.

2) Recurring chest colds.

3) Sinusitis.

4) Coughing , gagging , choking,

5)Middle ear infections

Answer: The respiratory wall or mucosa is made up of the epithelium and supporting lamina propria. The epithelium of respiratory tract is tall columnar pseudostratified with CILIA and goblet cells The cilia aids in sweeping away dusts and bacteria that adheres to the mucous on the epithelium. Therefore people with Primary ciliary dyskinesia are prone to Respiratory infections.

Explanation: Primary ciliary dyskinesia also called immotile ciliary syndrome is a rare genetic disease that affects the movement of cilia lining the respiratory tract. The major consequences of this dysfunction is reduced or absent mucus clearance from the lungs which subsequently leads to chronic recurrent respiratory infections

I hope this helps. Thanks!

Tadpoles raised in water with atrazine levels of 0.1 ppb should produce a higher percentage of male frogs with gonadal abnormalities than those raised in pure water.
This statement is an example of:

A. a question leading to a hypothesis
B. a hypothesis
C. a testable prediction leading to design of an experiment
D. data from an experiment
E. an interpretation of data

Answers

Answer:

Option C, a testable prediction leading to design of an experiment

Explanation:

The statement here predicts the outcomes of raising tadpoples is water with atrazine levels of 0.1 ppb as compared to the ones raised in pure water. Hence, it cannot be question. Now since this prediction can be tested, an experiment can be designed where a certain number of tadpoles can be raised in pure water and the same number of tadpoles can be raised in water with 0.1ppb of atrazine level. The difference in two populations can be then compared to either support the prediction or contradict it.

Hence, option C is correct

6) (1 point) Proteins that span biological membranes often contain -helices. Given that the insides of membranes are highly hydrophobic, predict what type of amino acids would be in such a helix. Why is an  helix particularly suited to exist in the hydrophobic environment of the interior of a membrane?

Answers

Answer:

The amino acids in such a helix would be hydrophobic in nature.

An α helix is particularly suited to cross a membrane because all of the carbonyl oxygen atoms and the hydrogen atoms of amide of the peptide backbone take part in intrachain hydrogen bonds, thus stabilizing these polar atoms in a hydrophobic environment.

Explanation :

Many transmembrane protiens use several alpha-helices wrapped up together.

It is usually seen as the helical structure can internally satisfy all the hydrogen-bonds , it doesn't leave any polar groups that are exposed to membrane if the sidechains are hydrophobic.

Sometimes, 2 to 3 alpha helices will wrap around each other , forming coiled coil. In an aphipathic alpha helix , the hydrophobic R groups on one side of each helix interact with each other while the hydrophilic R groups on the other side of each helix will interact with water.

Answer:

→alpha-helices

→Non-polar Amino acids

→because they and non -polar and hydrophobic.

Explanation:

Membrane proteins can be intrinsic (integral ) that is embedded in the membrane bilayer or extrinsic(peripheral) attached to the outer membrane layer.

These  integral protein transcend  the entire phospholipid bilayer, with the alpha- helices. The latter have hydrophobic side chains of non-polar amino acids. They are held to  the cell membrane  with  these  side chains  which forms hydrophobic interactions   with fatty acyl group of the  phosphoslipid  bilayer, and  sometimes  ionic bond with the polar head of phospholipid.

These alpha helix are non-polar(uncharged) and hydrophobic.A characteristic  feature that make them  to   interact and fixed into  the integral   phospholipid hydrophobic medium.

You are running a nursery for garden peas at Baton Rouge, and you have two pure-bred garden pea strains: Yellow Wrinkled [YYrr] and Green Round [yyRR]. You know that Yellow is dominant to Green, and also that Round is dominant to Wrinkled. One customer dropped by and asked about one particular pure-bred strain, Yellow Round [YYRR]. You promised to that customer that you could generate that strain next year through the following breeding experiments.
I. Crossing pure-bred Yellow Wrinkled with Green Round
II. Self-crossing F1 progeny
III. Screening pure-bred Yellow Round among the F2 progeny

What is the genotype for F1 progeny?

A. YYrr
B. rrYY
C. YyRr
D. yyrr
E. none of the above

Answers

Answer:

C. YyRr

Explanation:

The cross was done between pure-bred Yellow Wrinkled and Green Round plants. The genotype of the pure breeding yellow wrinkled parent plant: YYrr. The genotype of the pure breeding green round parent plant: yyRR.

A cross between YYrr and yyRR would obtain the progeny in the following ratios:

YYrr x yyRR= All YyRr (yellow and round)

Non-segmentation allows for evolutionary innovation in body form.
a. True
b. False​

Answers

Answer:

True.

Explanation:

Answer: a. True

Explanation: Through evolutionary time, animals have developed more-complex body plans, including  true tissues, non-segmentation and bilateral symmetry which is possible as a result of evolutionary innovation--the introduction and progression of novel traits compared to what exists before leading to a more advanced or complex form. Non-segmentation indeed allows for evolutionary innovation in body form.

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