PLEASEEE HELP!! Ill mark brainlist

How/why does the DNA separate?
Discuss porosity or pores, electricity, DNAS charge & size of DNA pieces. Highlight all the 4 terms

Answers

Answer 1

Electrophoresis is a technique commonly used in the lab to separate charged molecules, like DNA, according to size.

Gel electrophoresis is a technique commonly used in laboratories to separate charged molecules like DNA?, RNA? and proteins? according to their size.

Charged molecules move through a gel when an electric current is passed across it.

An electric current is applied across the gel so that one end of the gel has a positive charge and the other end has a negative charge.

The movement of charged molecules is called migration. Molecules migrate towards the opposite charge. A molecule with a negative charge will therefore be pulled towards the positive end (opposites attract!).

The gel consists of a permeable matrix, a bit like a sieve, through which molecules can travel when an electric current is passed across it.

Smaller molecules migrate through the gel more quickly and therefore travel further than larger fragments that migrate more slowly and therefore will travel a shorter distance. As a result the molecules are separated by size.

Gel electrophoresis and DNA

Electrophoresis enables you to distinguish DNA fragments of different lengths.

DNA is negatively charged, therefore, when an electric current is applied to the gel, DNA will migrate towards the positively charged electrode.

Shorter strands of DNA move more quickly through the gel than longer strands resulting in the fragments being arranged in order of size.

The use of dyes, fluorescent? tags or radioactive? labels enables the DNA on the gel to be seen after they have been separated. They will appear as bands on the gel.

A DNA marker with fragments of known lengths is usually run through the gel at the same time as the samples.

By comparing the bands of the DNA samples with those from the DNA marker, you can work out the approximate length of the DNA fragments in the samples.

How is gel electrophoresis carried out?

Preparing the gel

Agarose gels? are typically used to visualise fragments of DNA. The concentration of agarose used to make the gel depends on the size of the DNA fragments you are working with.

The higher the agarose concentration, the denser the matrix and vice versa. Smaller fragments of DNA are separated on higher concentrations of agarose whilst larger molecules require a lower concentration of agarose.

To make a gel, agarose powder is mixed with an electrophoresis buffer and heated to a high temperature until all of the agarose powder has melted.

The molten gel is then poured into a gel casting tray and a “comb” is placed at one end to make wells for the sample to be pipetted into.

Once the gel has cooled and solidified (it will now be opaque rather than clear) the comb is removed.

Many people now use pre-made gels.

The gel is then placed into an electrophoresis tank and electrophoresis buffer is poured into the tank until the surface of the gel is covered. The buffer conducts the electric current. The type of buffer used depends on the approximate size of the DNA fragments in the sample.

Preparing the DNA for electrophoresis

A dye is added to the sample of DNA prior to electrophoresis to increase the viscosity of the sample which will prevent it from floating out of the wells and so that the migration of the sample through the gel can be seen.

A DNA marker (also known as a size standard or a DNA ladder) is loaded into the first well of the gel. The fragments in the marker are of a known length so can be used to help approximate the size of the fragments in the samples.

The prepared DNA samples are then pipetted into the remaining wells of the gel.

When this is done the lid is placed on the electrophoresis tank making sure that the orientation of the gel and positive and negative electrodes is correct (we want the DNA to migrate across the gel to the positive end).

Separating the fragments

The electrical current is then turned on so that the negatively charged DNA moves through the gel towards the positive side of the gel.

Shorter lengths of DNA move faster than longer lengths so move further in the time the current is run.

The distance the DNA has migrated in the gel can be judged visually by monitoring the migration of the loading buffer dye.

The electrical current is left on long enough to ensure that the DNA fragments move far enough across the gel to separate them, but not so long that they run off the end of the gel.

Illustration of DNA electrophoresis equipment used to separate DNA fragments by size. A gel sits within a tank of buffer. The DNA samples are placed in wells at one end of the gel and an electrical current passed across the gel. The negatively-charged DNA moves towards the postive electrode. Image credit: Genome Research Limited

tank.


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Citric acid cycle also known as the Krebs cycle, is the second stage of the three-stage process by which living cells break down organic fuel molecules in the presence of oxygen to harvest the energy they need to grow and divide.

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Explanation: Hope this helps? .-.

Item 3
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Tucker and Micayla are conducting an experiment about cellular respiration. The purpose of their experiment is to find out if plant cells utilize celluid!
respiration in addition to photosynthesis. They begin by filling one test tube with glass beads, one with dried (non-germinating) peas, and one with
peas that have been soaked and have begun to germinate
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eat
make
oxygen
Look at the diagram. A product of cellular respiration is
A reactanto cellular respiration is
energy for
The differences that plants first
respiration, whereas animals must
which can escape from the test tubes through the
which will be used up. Plants, like animals, need
food that later undergoes cellular
food
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Question 22
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Answers

Cellular respiration is commonly described as a metabolic pathway that reduces glucose and produces ATP. The answers are in the bullet point below:

The test group will undergo cellular respiration is the germinating peas. This is because they have been placed in an environment/conditions aid or  start to grow. This implies hat they are the only test group that can under cellular respiration. They  ATP for their growth.

A product of cellular respiration is carbon dioxide, which can escape from the test tubes throw the pipettes. A reactant of cellular respiration is oxygen, which will be used up. Plants, like animals, need energy for growth and reproduction. The difference is the plants first make, food, then undergo cellular respiration, whereas animals must eat, food, then undergo cellular respiration to make the energy from food available.

In Cellular respiration process, organisms utilizes the oxygen so as to break down food molecules and in turn produce chemical energy for cell functions.

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Tucker and Micayla are conducting an experiment with cellular respiration. The purpose of their experiment is to find out if plant cells utilize cellular respiration in addition to photosynthesis. They begin by filing one test tube with glass beads, one with dried (non-germinating) peas, and one with peas that have been soaked and have begun to germinate. Look at the diagram. Predict which test group will undergo cellular respiration and explain why.

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Non-renewable energy may be defined as that energy that will run out or will not be replenished for thousands or even millions of years.

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Answer:

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Explanation:

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Explanation:

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Lactase breaks down only lactose in food in our body can absorb it not maltose and sucrose as enzymes are specific in nature.

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Answer:

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Answer:

Fuses and Circuit Breakers both serve the same purpose – which is to protect electrical circuits by preventing overloads that can cause fires. They both interrupt the flow of electricity, but in very different ways from each other

Explanation:

Hope I could help

                            Please mark as brailiest

What happens when an action potential is produced with a signal that is stronger than threshold?

A)
weaker action potential generated

B)
no action potential generated

C)
action potential has same strength as threshold

D)
stronger action potential generated

Answers

Answer:

C) action potential has same strength as threshold

Explanation:

What happens when an action potential is produced with a signal that is stronger than threshold action potential has same strength as threshold

When an action potential is produced with a signal that is stronger than the threshold, the resulting action potential is typically stronger or more intense compared to a standard action potential. The answer is D) Stronger action potential generated.

The threshold is the minimum level of depolarization required to initiate an action potential in a neuron. If the signal surpasses the threshold, it means that the depolarization is greater than what is necessary to trigger the action potential.

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Answer:

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Answer:

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Answer:

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Explanation:

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Answers

Answer:

English is not my native language so sry if there's any grammaticaly mistake

Explanation:

cuz it changes its shape and forme u got that?!

Lactose falls off its binding site at the operator because the allolactose binds to the repressor causing it to fall off the operator side.

What do you mean by Lac repressor?

Lac repressor prevents the transcription of genes involved in lactose utilization in E. coli, such as lac genes.

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Therefore, Lactose falls off its binding site at the operator because the allolactose binds to the repressor causing it to fall off the operator side.

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Answer:

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Answers

Answer:

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Explanation:

In prophase 1, homologous chromosomes pair up and exchange sections of DNA in a process called crossing over.

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Answer:

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Explanation:

I remember that carbon can be toxic if it's increased

Answer:

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Explanation:

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