Discuss the mobility of different sizes and shape of the DNA on the agarose gel, and...
Homework Answers
Agarose is a porous substance and here DNA moves from negative electrode to positive electrode. . So it can isolate DNA according to their size and shape. The DNA which is smaller in size moves faster in comparison to DNA of larger size. So, in a gel, large sized DNA remain in the upper portion, near the negative pole and small sized DNA molecules remain towards the positive pole. Intermediate sized DNA remain in between depending upon their size.
Depending upon shape, Nicked DNA remain in the upper portion, hen remain the linear DNA. Below linear DNA, remain the supercoiled DNA and below it remain the circular, single stranded DNA molecules.
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Discuss the mobility of different sizes and shape of the DNA
on the agarose gel, and...
EXERCISE 17.2: Sketch an agarose gel for use in separating DNA. Make sure you label: (a) The location of the wells (b) T...
EXERCISE 17.2: Sketch an agarose gel for use in separating DNA. Make sure you label: (a) The location of the wells (b) The positive electrode (c) The negative electrode ( d) The direction of migration of the DNA in the gel
The picture above represents an agarose gel that was used to analyze plasmid DNA after it...
The picture above represents an agarose gel that was used to analyze plasmid DNA after it was cut with the restriction enzyme HindIll. The plasmid was incubated with Hindill until all of the available Hindlll cut sites were cut by HindIll. After running the sample on the gel, three bands were detected (Note that there are three wells shown at the top of the gel for loading samples, however, only the middle well was loaded with sample). Based on this...
During gel electrophoresis, DNA travels towards the positive charge. Including the substance agarose in the gel...
During gel electrophoresis, DNA travels towards the positive charge. Including the substance agarose in the gel allows for visualization of DNA under UV light. Below is an image of a gel run with a single DNA sample (ane 2) and a DNA ladder (lane 1). Using the DNA ladder reference included to the right, it can be concluded that two fragments labeled C&D in the DNA sample are approximately 6.0 Lane 1 2 kilobases and 3.0 kilobsases, respectively. Laai Auxilwa...
Which of the following best describes how the migration of DNA in an agarose gel will...
Which of the following best describes how the migration of DNA in an agarose gel will be changed following incubation of the DNA with a topoisomerase? Gel migration is changed, because nucleotides are isomerized from the D to L configuration Gel migration is changed, because compactness is changed Gel migration is changed, because the total charge of the phosphate backbone is reduced Gel migration is unaffected, because the number of base pairs is increased
In an experiment with agarose gel eletrophoresis, the DNA samples are loaded in the wells within...
In an experiment with agarose gel eletrophoresis, the DNA samples are loaded in the wells within the gel and the electric current is turned on. When observing the samples, you notice that the DNA fragments are moving in the opposite (wrong) direction. What possible error could have caused this to occur?
Stuck answering the rest of these 3. Application of DNA gel electrophoresis. DNA gel electrophoresis is...
Stuck answering the rest of
these
3. Application of DNA gel electrophoresis. DNA gel electrophoresis is commonly used in determining familial relationships among individuals, for ex; to establish paternity of a child. This technique is called DNA fingerprinting. In this technique the DNA of parents and children is roughly chopped up into pieces and resolved on an agarose gel. The DNA ill resolve according to their sizes and create a pattern or a "fingerprint". The fingerprint of the child is...
What would happen to DNA if the gel tray within an electrophoresis chamber were placed incorrectly,...
What would happen to DNA if the gel tray within an electrophoresis chamber were placed incorrectly, with the wells closest to the positive electrode? Choose one: A. DNA would remain in the gel. B. DNA bands would appear smeared. C. DNA would be pulled through the gel in the wrong direction. D. DNA would not fluoresce under UV light.
1. List the ingredients required for PCR. 2. How does DNA move down the agarose gel?...
1. List the ingredients required for PCR. 2. How does DNA move down the agarose gel? What forces aid in this? Meaning, how does gel electrophoresis work? 3. What do the chelex beads do? 4. Why is DNA important?
A 1.2% Agarose Gel will separated DNA based on . O charge only both charge and size O size only n...
Please give clear answers along
with detailed explanations. Thank you so much!
A 1.2% Agarose Gel will separated DNA based on . O charge only both charge and size O size only neither charge nor size Question 2 A 1.2% Agarose Gel will separated dyes, proteins and amino acids based on . charge only both charge and size Osize only neither charge nor size Methylene Blue is a positively-charged dye. Which of the following components of DNA will it bind?...
After PCR is performed the products are run out on an agarose gel. In the figure...
After PCR is performed the products are run out on an agarose
gel. In the figure below, grey bands represent the wells the PCR
product was loaded into. The white bands represent DNA fragments
produced by PCR. The target fragment amplified by the primers was
1,500 bp in size.
The ladder is a standard DNA ladder containing bands of various
sizes between 5,000 and 1,000 bp. The negative control contained
only molecular grade water*. The positive control contained DNA
known...
The picture above represents an agarose gel that was used to analyze plasmid DNA after it was cut with the restriction enzyme HindIll. The plasmid was incubated with Hindill until all of the available Hindlll cut sites were cut by HindIll. After running the sample on the gel, three bands were detected (Note that there are three wells shown at the top of the gel for loading samples, however, only the middle well was loaded with sample). Based on this...
During gel electrophoresis, DNA travels towards the positive charge. Including the substance agarose in the gel allows for visualization of DNA under UV light. Below is an image of a gel run with a single DNA sample (ane 2) and a DNA ladder (lane 1). Using the DNA ladder reference included to the right, it can be concluded that two fragments labeled C&D in the DNA sample are approximately 6.0 Lane 1 2 kilobases and 3.0 kilobsases, respectively. Laai Auxilwa...
Stuck answering the rest of
these
3. Application of DNA gel electrophoresis. DNA gel electrophoresis is commonly used in determining familial relationships among individuals, for ex; to establish paternity of a child. This technique is called DNA fingerprinting. In this technique the DNA of parents and children is roughly chopped up into pieces and resolved on an agarose gel. The DNA ill resolve according to their sizes and create a pattern or a "fingerprint". The fingerprint of the child is...
1. List the ingredients required for PCR. 2. How does DNA move down the agarose gel? What forces aid in this? Meaning, how does gel electrophoresis work? 3. What do the chelex beads do? 4. Why is DNA important?
Please give clear answers along
with detailed explanations. Thank you so much!
A 1.2% Agarose Gel will separated DNA based on . O charge only both charge and size O size only neither charge nor size Question 2 A 1.2% Agarose Gel will separated dyes, proteins and amino acids based on . charge only both charge and size Osize only neither charge nor size Methylene Blue is a positively-charged dye. Which of the following components of DNA will it bind?...
After PCR is performed the products are run out on an agarose
gel. In the figure below, grey bands represent the wells the PCR
product was loaded into. The white bands represent DNA fragments
produced by PCR. The target fragment amplified by the primers was
1,500 bp in size.
The ladder is a standard DNA ladder containing bands of various
sizes between 5,000 and 1,000 bp. The negative control contained
only molecular grade water*. The positive control contained DNA
known...
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