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HighTide

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Re: VCE Biology Question Thread
« Reply #5325 on: June 30, 2015, 06:54:50 pm »
+2
I just had a question regarding genes and such. What exactly determines why a gene (or is it an allele?) is dominant over another? I have tried looking it up but my bio knowledge is only around a year 10 level and I can't really comprehend a lot of the answers. If i remember correctly, alleles are just pairs of genes that code for a specific phenotype. How does one of them overpower the other.

Sorry if its off-topic, just curious :)
Genes are sequences of nucleotides coding for protein. They can have different alleles. Alleles are alternative forms of the gene. These are what you inherit from parents. Variation occurs due to the crossing over and formation of chiasmata.
You can have either dominant or recessive alleles for the trait.
-Dominant alleles express in presence and absence of a recessive allele.
-Recessive alleles only express in the absence of dominant alleles.
These definitions may seem unnecessary, but you need to understand these. Now that they have been established...
Remember that the genes are transcribed and translated to create proteins. The production of these proteins is regulated by promoter and regulatory sequences and etc. (learnt during transcription and translation in VCE). One doesn't necessarily overpower the other. It's just that one is expressed and the other is masked or not expressed (in complete dominancy).

By the way, it's not that a gene is dominant over another. It's the allele. The alleles determine whether the gene expresses.
Interesting for your question about alleles, I feel I have not 100% answered it. Do you need more detail, as to like how an allele links into gene expression? The main idea is that it controls whether a gene is expressed or not. For more information, there are many examples like melanin in eyes or eye colour of Drosophila and etc.
Hope this helps  :) If you need, I may be able to help out.
« Last Edit: June 30, 2015, 06:58:03 pm by HighTide »
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Floatzel98

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Re: VCE Biology Question Thread
« Reply #5326 on: June 30, 2015, 07:49:17 pm »
0
Genes are sequences of nucleotides coding for protein. They can have different alleles. Alleles are alternative forms of the gene. These are what you inherit from parents. Variation occurs due to the crossing over and formation of chiasmata.
You can have either dominant or recessive alleles for the trait.
-Dominant alleles express in presence and absence of a recessive allele.
-Recessive alleles only express in the absence of dominant alleles.
These definitions may seem unnecessary, but you need to understand these. Now that they have been established...
Remember that the genes are transcribed and translated to create proteins. The production of these proteins is regulated by promoter and regulatory sequences and etc. (learnt during transcription and translation in VCE). One doesn't necessarily overpower the other. It's just that one is expressed and the other is masked or not expressed (in complete dominancy).

By the way, it's not that a gene is dominant over another. It's the allele. The alleles determine whether the gene expresses.
Interesting for your question about alleles, I feel I have not 100% answered it. Do you need more detail, as to like how an allele links into gene expression? The main idea is that it controls whether a gene is expressed or not. For more information, there are many examples like melanin in eyes or eye colour of Drosophila and etc.
Hope this helps  :) If you need, I may be able to help out.
Thanks for that. It doesn't all make total sense to me, but it does help. I think i will just go watch some Khan Academy to satisfy my cravings :) Might as well start from the start instead of diving in halfway through. Thanks for your help
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BakedDwarf

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Re: VCE Biology Question Thread
« Reply #5327 on: June 30, 2015, 10:47:55 pm »
0
Hey guys!! I've read over my unit 3 and 4 notes and got a plethora of questions regarding uncertainties about my expressions and the biology coursework. Hopefully someone can answer these questions. Thanks.

Unit 3 AoS 1
1. Is a cell limited to the size it grows because it reaches a point where it is unable to sufficiently carry out the
    exchange of materials with the environment?
2. What's the structural difference between starch, glycogen and cellulose?
3. What are glycolipids and glycoproteins? What are their functions?
4. What would you say the MAIN differences between necrosis and apoptosis are? Like I know apoptosis is a
    programmed cell death and necrosis is not, and necrosis is caused my traumatic damage. But what is/are the
    MAIN difference/s?
5. Is rational drug design an artificial method of inhibiting the enzyme active site by studying the biology of an
    organism and using this knowledge to develop a drug that acts as a competitive inhibitor against the enzyme?
    (not sure if this makes much sense)

U3 AoS 2
1. Do we need to know about exteroceptors (e.g. chemoreceptors etc)?
2. Signal transduction is a set of chemical reactions in a cell that occurs when a molecule attaches to a receptor on
    the cell membrane. Is this correct?
3. In how much detail should be know the plant hormones? My understanding in plant growth regulators is based
    around A+ biology notes (see below for an attached screenshot from A+ biology notes)
4. Do we need to know about autocrine, paracrine and endocrine signalling for the exam?
5. Do we need to know what neurohormones are? If so, what are they? (I didn't see anything about them in my
    textbook...)

U4 AoS 1
1. How thoroughly do we need to know the process of meiosis? Do we need to know what exactly happens in each
    step, such as telophase 1, anaphase 2, etc?
2. Is this the correct definition of binary fission? Binary fission is the division of a prokaryotic cell into two by
    replicating its single DNA strands
 into two and separating (plasma membrane and cell wall furrow inwards and
    divides the
 cytoplasm resulting in 2 daughter cells)
3. Is it required to know RNA interference (RNAi); that is, how we turn off genes artificially? (I didn't see this in my
    textbook so i'm not too sure)
4. Aneuploidy when two homologous chromosomes, instead of
 separating during meiosis, go into the same cell,
    which results in gametes with an extra chromosome or missing a chromosome. Whereas polyploidy is when cell
    division fails all together, hence two gametes have two sets of chromosomes and the other two have no
    chromosomes. Is this correct?
5. The regions of DNA used in DNA profiling are short tandem repeats (STRs) and variable nucleotide tandem
    repeats (VNTRs); they are both a short non-coding region of DNA that are repeated many times in the genome of
    an organism and they vary considerably between individuals in terms of the numbers of the repeating unit. STRs
    have a repeat sequence of two to five bases and VNTRs have a repeat sequence of more than five bases. Is this
    correct?

pi

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Re: VCE Biology Question Thread
« Reply #5328 on: June 30, 2015, 11:14:45 pm »
+2
Hey guys!! I've read over my unit 3 and 4 notes and got a plethora of questions regarding uncertainties about my expressions and the biology coursework. Hopefully someone can answer these questions. Thanks.

WE CAN DO THIS, I'll take your first batch for the team and leave the rest coz sharing is caring. I can't be bothered typing out full answers for everything, so I'll provide some clues at times! :)

1. Is a cell limited to the size it grows because it reaches a point where it is unable to sufficiently carry out the
    exchange of materials with the environment?

Of course! Think about SA:V and whether a cell will be able to survive if it becomes big, say the size of a frisbee :P

2. What's the structural difference between starch, glycogen and cellulose?

Again, of course! If there were no differences, these polymers would be the same :P

Best learnt pictorially, pay particular attention to amount of branching and think about how that relates to function:


3. What are glycolipids and glycoproteins? What are their functions?

Think about the names and break them down, helps with anything in bio:
- glyco-lipids = carbohydrate + lipid
- glyco-protein = carbohydrate + protein

They have various roles depending on the specific molecule, they have roles in cell signalling etc etc But they also have clinically relevant functions too (think of the ABO system!).

4. What would you say the MAIN differences between necrosis and apoptosis are? Like I know apoptosis is a
    programmed cell death and necrosis is not, and necrosis is caused my traumatic damage. But what is/are the
    MAIN difference/s?

Pretty much nailed the main difference. Apoptosis is "normal" and "planned", necrosis is "abnormal" and "unplanned".

The specifics of each pathway differ as well, again pictures are your friend:



5. Is rational drug design an artificial method of inhibiting the enzyme active site by studying the biology of an
    organism and using this knowledge to develop a drug that acts as a competitive inhibitor against the enzyme?
    (not sure if this makes much sense)

I direct you to this fantastic answer (and subsequent replies) that I had bookmarked for this moment! Re: Rational drug design

mahler004

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Re: VCE Biology Question Thread
« Reply #5329 on: June 30, 2015, 11:47:34 pm »
+1
2. Signal transduction is a set of chemical reactions in a cell that occurs when a molecule attaches to a receptor on
    the cell membrane. Is this correct?

Yep, that's the gist of it. Wikipedia defines it well - it's a series of biochemical events that occur in a cell after a receptor is stimulated, leading to a final biological outcome. There's also a (very simplified) diagram of some of the signal transduction pathways in cells:



Yes, that's the simplified diagram! Signal transduction is very complicated.

Regarding rational drug design - it's worth mentioning (although beyond VCE) that a lot of drug companies are moving away from rational drug design. It's certainly a useful approach - but not quite as productive as you might expect. Current approaches to drug design seem to be moving back to fragment screening/more 'empirical' approaches. It also doesn't fit well to 'biologicals'/immunotherapies which are currently pretty popular. I don't really want to bump a three year old thread, so I'll just make this point here.

The overall point of learning about rational drug design in VCE is really a 'case study' to show how learning about how understanding an organism's biology can give you useful (and lucrative!) outcomes.
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HighTide

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Re: VCE Biology Question Thread
« Reply #5330 on: July 01, 2015, 08:11:56 am »
+1
Hey guys!! I've read over my unit 3 and 4 notes and got a plethora of questions regarding uncertainties about my expressions and the biology coursework. Hopefully someone can answer these questions. Thanks.
U3 AoS 2
1. Do we need to know about exteroceptors (e.g. chemoreceptors etc)?
2. Signal transduction is a set of chemical reactions in a cell that occurs when a molecule attaches to a receptor on
    the cell membrane. Is this correct?
3. In how much detail should be know the plant hormones? My understanding in plant growth regulators is based
    around A+ biology notes (see below for an attached screenshot from A+ biology notes)
4. Do we need to know about autocrine, paracrine and endocrine signalling for the exam?
5. Do we need to know what neurohormones are? If so, what are they? (I didn't see anything about them in my
    textbook...)
Hi!
1. Yes you do.
2. As Mahler004 said, it's a cascade of biochemical events occurring after the cell is stimulated until its response.
3. That is probably enough. However, probably familiarize yourself with how it occurs. For example, how do auxins cause the bending of a plant's shoot for phototropism?
4. Yes, you do require knowledge of those. There's also contact-dependent signalling.
5. Yes. Neurohormones are the hormones produced by nerve cells. There are quite a bit of them. The ones they can ask will most likely be ADH, Vasopressin or Oxytocin. These are secreted by neurosecretory cells (very original naming) which are part of the neuroendocrine system. Definitely good to get an understanding of the concept. For us, it did come up in a SAC last year.
Hey guys!! I've read over my unit 3 and 4 notes and got a plethora of questions regarding uncertainties about my expressions and the biology coursework. Hopefully someone can answer these questions. Thanks.
U4 AoS 1
1. How thoroughly do we need to know the process of meiosis? Do we need to know what exactly happens in each
    step, such as telophase 1, anaphase 2, etc?
2. Is this the correct definition of binary fission? Binary fission is the division of a prokaryotic cell into two by
    replicating its single DNA strands
 into two and separating (plasma membrane and cell wall furrow inwards and
    divides the
 cytoplasm resulting in 2 daughter cells)
3. Is it required to know RNA interference (RNAi); that is, how we turn off genes artificially? (I didn't see this in my
    textbook so i'm not too sure)
4. Aneuploidy when two homologous chromosomes, instead of
 separating during meiosis, go into the same cell,
    which results in gametes with an extra chromosome or missing a chromosome. Whereas polyploidy is when cell
    division fails all together, hence two gametes have two sets of chromosomes and the other two have no
    chromosomes. Is this correct?
5. The regions of DNA used in DNA profiling are short tandem repeats (STRs) and variable nucleotide tandem
    repeats (VNTRs); they are both a short non-coding region of DNA that are repeated many times in the genome of
    an organism and they vary considerably between individuals in terms of the numbers of the repeating unit. STRs
    have a repeat sequence of two to five bases and VNTRs have a repeat sequence of more than five bases. Is this
    correct?
1. Yes. This is probably more to do with understanding, but it's essential. If you can understand the individual things occurring during meiotic division, there's not much you can lose a mark on. It will also help you in doing application questions.
2. That seems very verbose. Binary fission is the amitotic and asexual division of prokaryotic cells. It is known that single-celled eukaryotes can do binary fission, but that's outside the scope of VCE.
3. Um I think RNA interference is well outside the syllabus. But it's basically a method of silencing the genes to prevent them from expressing. It's not just artificial, because it does happen in nature. It's just that it can be done in a laboratory. For example: to silence genes which cause disease conditions.
4. Not really, I believe you got aneuploidy correct but remember it is the general term to describe the condition where an organism has an abnormal number of chromosomes. Polyploidy falls under the category of aneuploidy. Polyploidy is an accident of cell division. But, it's when the organism has more than two sets of complete chromosomes. What you may be referring to is non-disjunction.
5. Yep that's correct.
Good luck  :)
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2016-2018: Bachelor of Biomedical Science

cosine

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Re: VCE Biology Question Thread
« Reply #5331 on: July 01, 2015, 09:44:24 am »
0
Hey guys, I have a few questions about Unit 3 Biology that I either did not understand or I still have knowledge gaps about, hopefully someone can help me :D

Cellular respiration:

1). How does glucose enter a cell for the uptake of glucose so that cellular respiration can occur? Does glucose just simply go along the concentration gradient from the extracellular fluids down into the cell through facilitated diffusion?

2). Once glucose has entered a cell, how exactly is it broken down into the 2, 2-Carbon molecules (pyruvate)? Does this reaction happen under the facilitation of enzymes and ATP?

3). Do we need to know that 2ATP molecules are used up in glycolysis, but 4ATP molecules are produced, meaning a net production of 2 ATP molecules are made during glycolysis?

4). Why is there a carrier molecule involved in glycolysis? Does this carrier molecule just pick up hydrogen ions and electrons to transport into the krebs cycle/electron transport chain?

5). Do we need to know the inputs/outputs of the krebs cycle with specific numbers, like 3CO2 molecules are produced for each pyruvate, 4NADH and 1FADH2?

6). Do we need to know about coenzyme A? (The molecule which reacts with pyruvate to produce CO2 and NADH)

7). How many ATP molecules occur during the krebs cycle? Is it just 1 per pyruvate?

8). How much do we need to know about the electron transport chain? Is it okay to just know that most of the ATP production occurs during this process, and that this occurs in the inner membrane of the mitochondria?

9). 2 ATP are made during glycolysis, 2 ATP during krebs cycle, and 34 in the ETC. Total of 38 ATP right?

10). Why does glucose break down to form ATP? Is it just because it is easier for the body to use smaller molecules as a means of energy, rather than the massive molecule glucose?

11). How much do we need to know about anaerobic respiration? Is it just that in animals, without oxygen the pyruvate is converted into lactic acid, and in plants into ethanol (alcohol)?

12). Does krebs cycle use oxygen? My guess is yes, because pyruvate is a 3-carbon molecule, and is converted into carbon dioxide, so I would think that oxygen is required for the process?


Signalling:

1). I know the importance of the reflex arc, but how does it actually work? Is the stimulus detected, and then the sensory neurones bypass the brain, and go straight to the spinal cord (does this mean the spinal cord is the control centre in this case?) and then from there motor neurones order the effector to act?

2). Do we need to know the feedback loops for the exam?

3). Is the main difference between negative and positive feedback that negative is trying to eliminate the stimulus, much like it's a bad thing, whereas positive feedback just enhances the stimulus?

4). Do neurones communicate with normal body cells? If so, how do they do this?

5). What detect the stimulus? Like If you put your hand on a hot surface, is it the mechanoreceptors that detect the stimulus, or is it the sensory neurones?

6). What's the difference between PNS and CNS? Is the central nervous system the neurones involved in the brain and spinal cord, whereas the peripheral nervous system is the outer network of neurones in the rest of the body?

7). Are interconnecting neurones found in the brain/spinal cord, or only brain? What do these neurones do?


Thanks so much if anyone can help :)


2016-2019: Bachelor of Biomedicine
2015: VCE (ATAR: 94.85)

cosine

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Re: VCE Biology Question Thread
« Reply #5332 on: July 01, 2015, 01:51:36 pm »
0
Few more questions from a Neap Exam:

Question 10:
i. Concentration of CO2 in the leaf
ii. Concentration of the O2 in the leaf
iii. Temperature

Which factors affect the output of the light-independent reactions of photosynthesis in plants?

Answer: All of the above.

My confusion: I understand how concentration of CO2 affects the output, because it is a vital component of the independent cycle, and temperature I understand, but how does the concentration of the oxygen affect the output? Isn't oxygen the byproduct of the light dependent stage, so what has this to do with the independent stage?


Question 11:
An electron transport chain is an essential part of the following cellular processes of?

Answer: Aerobic respiration and photosynthesis.

My confusion: I know the electron transport chain occurs in cellular respiration, and I think i also knew about it in photosynthesis during the light dependent stage, but are we required to know that ETC also occurs during photosynthesis?

Question 2:
RNAP catalyses many steps in the process where DNA is converted into RNA. This is quite unusual in that most enzymes catalyse only one reaction. Using your understanding of enzyme structure and function, give one reason which would explain how RNAP can catalyse many steps.

Answer: Enzymes have many active sites for different substrates OR the RNAP can be a quaternary structured enzyme

My confusion: Would this ever be a VCAA question? I mean i never knew enzymes had more than one active site, do they even or is Neap just weird? My original answer was that there many be several substrates that are complementary to the enzyme's active site.

General questions:

- Do we need to know the chemical formula for cellular respirations?
- Can someone please list the required info to include in an experiment designing question?

Thanks :D
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2015: VCE (ATAR: 94.85)

BakedDwarf

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Re: VCE Biology Question Thread
« Reply #5333 on: July 01, 2015, 02:33:27 pm »
0
many thanks Pi, mahler004 and HighTide.

vox nihili

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Re: VCE Biology Question Thread
« Reply #5334 on: July 01, 2015, 03:22:16 pm »
+3
Hey guys, I have a few questions about Unit 3 Biology that I either did not understand or I still have knowledge gaps about, hopefully someone can help me :D

Cellular respiration:

1). How does glucose enter a cell for the uptake of glucose so that cellular respiration can occur? Does glucose just simply go along the concentration gradient from the extracellular fluids down into the cell through facilitated diffusion?

2). Once glucose has entered a cell, how exactly is it broken down into the 2, 2-Carbon molecules (pyruvate)? Does this reaction happen under the facilitation of enzymes and ATP?

3). Do we need to know that 2ATP molecules are used up in glycolysis, but 4ATP molecules are produced, meaning a net production of 2 ATP molecules are made during glycolysis?

4). Why is there a carrier molecule involved in glycolysis? Does this carrier molecule just pick up hydrogen ions and electrons to transport into the krebs cycle/electron transport chain?

5). Do we need to know the inputs/outputs of the krebs cycle with specific numbers, like 3CO2 molecules are produced for each pyruvate, 4NADH and 1FADH2?

6). Do we need to know about coenzyme A? (The molecule which reacts with pyruvate to produce CO2 and NADH)

7). How many ATP molecules occur during the krebs cycle? Is it just 1 per pyruvate?

8). How much do we need to know about the electron transport chain? Is it okay to just know that most of the ATP production occurs during this process, and that this occurs in the inner membrane of the mitochondria?

9). 2 ATP are made during glycolysis, 2 ATP during krebs cycle, and 34 in the ETC. Total of 38 ATP right?

10). Why does glucose break down to form ATP? Is it just because it is easier for the body to use smaller molecules as a means of energy, rather than the massive molecule glucose?

11). How much do we need to know about anaerobic respiration? Is it just that in animals, without oxygen the pyruvate is converted into lactic acid, and in plants into ethanol (alcohol)?

12). Does krebs cycle use oxygen? My guess is yes, because pyruvate is a 3-carbon molecule, and is converted into carbon dioxide, so I would think that oxygen is required for the process?


Signalling:

1). I know the importance of the reflex arc, but how does it actually work? Is the stimulus detected, and then the sensory neurones bypass the brain, and go straight to the spinal cord (does this mean the spinal cord is the control centre in this case?) and then from there motor neurones order the effector to act?

2). Do we need to know the feedback loops for the exam?

3). Is the main difference between negative and positive feedback that negative is trying to eliminate the stimulus, much like it's a bad thing, whereas positive feedback just enhances the stimulus?

4). Do neurones communicate with normal body cells? If so, how do they do this?

5). What detect the stimulus? Like If you put your hand on a hot surface, is it the mechanoreceptors that detect the stimulus, or is it the sensory neurones?

6). What's the difference between PNS and CNS? Is the central nervous system the neurones involved in the brain and spinal cord, whereas the peripheral nervous system is the outer network of neurones in the rest of the body?

7). Are interconnecting neurones found in the brain/spinal cord, or only brain? What do these neurones do?


Thanks so much if anyone can help :)

Thanks for actually trying to answer some of your own questions, an important thing to do in my view if you want to learn :)

Respiration:

1. Glucose transport is tricky. Glucose can enters cells via carrier proteins, but this process can be either active or passive. So glucose can enter cells via facilitated diffusion or active transport.

2. Correct. A series of ten reactions, collectively referred to as glycolysis, give rise to pyruvate from glucose. This process involves all sorts of enzymes/coenzymes etc. Naturally, all you need to know are the inputs and outputs.

3. It can't hurt knowing that, although I'm not convinced VCE examiners would be that pedantic.

4. Hmmm I'm not sure that carrier molecule is the correct word. I assume you're referred to NAD+/NADH. The reduction of NAD+ to NADH during glycolysis and Krebs is extremely important. Electrons and protons from NADH form the basis of the electron transport chain. You don't really need to know the details of this, however, other than that it happens.

5. Yes, you need to know the inputs and outputs of each stage.

6. Yes, CoA is an important part of the process. You don't need to know any more than that it reacts with pyruvate to form acetyl CoA, which is the molecule that enters the Krebs cycle.

7. Correct. Although, you are better to remember numbers per glucose. So it is two ATP per glucose. 

8. I think that that understanding would probably be sufficient. The details of the electron transport chain are well beyond what could reasonably be expected of year 12 biology students.

9. 32-34 in the ETC, leading to a total of 36-38. In truth, this number actually varies more widely; however, the VCE course represents it as such.

10. Kind of. Bonds contain energy. Therefore, if you break bigger molecules into smaller molecules, you release energy. This release of energy can be used to drive the production of other, bigger molecules. In the context of cellular respiration, the breaking of bonds is used to produce ATP from ADP and Pi, and also produce NADH from NAD+ and H.

11. You should know the inputs and outputs of fermentation and lactic acid production.

12. I'm glad that you had a guess on this one; it is wrong however. The only process that uses oxygen is the ETC. In the context of cellular respiration, oxygen is the so-called final acceptor, meaning that it takes the electrons from the ETC and uses them to react with hydrogen ions to form water.
If you look at the chemical structure of pyruvate, you will notice that it contains a number of oxygen atoms inherently. It is these atoms that go on to form carbon dioxide.

Signalling:

1. That's correct. Most signals from the body come back to the brain via the spinal cord, but in the case of a reflex arc, the sensory neurone interfaces directly with a motor neurone (or via an interneurone), meaning that a response is generated without input from the brain.

2. You don't need to know specific pathways—though having an example handy is a must. You should, however, be able to look at a pathway and explain how it works. YOu'll be given enough prompt material to explain how it works without having had to have seen the pathway before.

3. This is the difference. Negative feedback opposes the stimulus; whereas, positive feedback reinforces the stimulus.

4. I don't know what you mean by normal body cells. 

5. Mechanoreceptors are a type of sensory neurone. There are many different forms of sensory neurone: taste receptors, mechanoreceptors, nociceptors (pain), thermoreceptors and so on. Each of these sensory neurones responds to a different type of energy. In the context of a hot surface, the heat is likely to be registered by thermoreceptors and nociceptors. Heat is not a mechanical energy, so mechanoreceptors will be unresponsive to it.

6. Correct.

7. Interneurones are found in the brain and the spinal cord. They pass signals between the sensory system and the motor system and do a lot of the "planning" in the brain.
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BakedDwarf

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Re: VCE Biology Question Thread
« Reply #5335 on: July 01, 2015, 04:19:19 pm »
0
Can an antibody have two different antigen binding sites?

vox nihili

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Re: VCE Biology Question Thread
« Reply #5336 on: July 01, 2015, 04:24:20 pm »
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Can an antibody have two different antigen binding sites?

No*









*Technically they can be engineered to naturally have two different antigen binding sites, though this does not happen naturally. I've only mentioned this for interest's sake; on an exam, you would be marked wrong (and rightly so) if you said that they had two antigen binding sites.
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wyzandrea

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Re: VCE Biology Question Thread
« Reply #5337 on: July 01, 2015, 04:25:24 pm »
0
Thank you for your introduction. As soon as I get a question, I will come to you.

cosine

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Re: VCE Biology Question Thread
« Reply #5338 on: July 01, 2015, 04:41:49 pm »
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@Mr. T-Rav 

Thank you very much, and yes, I thought I would include my own understandings because I remember before my osmosis sac you told me off and said I should not ask questions without my answer to it :P

Signalling q4:

I mean that can neurones initiate a response in a body cell (they are all body cells, just realised) by this I meant a cell that is NOT a neurone :P

I know neurones release neurotransmitters that diffuse through the synaptic cleft into the post synaptic membrane receptors, can this post synaptic cell not be a neurone?
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Re: VCE Biology Question Thread
« Reply #5339 on: July 01, 2015, 06:32:02 pm »
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@Mr. T-Rav 

Thank you very much, and yes, I thought I would include my own understandings because I remember before my osmosis sac you told me off and said I should not ask questions without my answer to it :P

Signalling q4:

I mean that can neurones initiate a response in a body cell (they are all body cells, just realised) by this I meant a cell that is NOT a neurone :P

I know neurones release neurotransmitters that diffuse through the synaptic cleft into the post synaptic membrane receptors, can this post synaptic cell not be a neurone?
Of course - think about effector cells and the end result of stimulating a neural pathway.