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What else can I help you with?
What is the term for a plasmid that contains a foreign gene?
Recombiant DNA
Can plasmid DNA be used for 16srRNA amplification?
The 16s rRNA genes (rDNA) exist on genomic DNA. Therefore, plasmid has nothing to do with its amplification. However, if the 16s rRNA gene is cloned into the plasmid, it can be amplified.
How does a human insulin genes become part of a plasmid?
1. Scientists remove plasmids, small rings of DNA, from bacterial cells. 2. An enzyme cuts open the plasmid DNA. The same enzyme removes the human insulin gene from its chromosome. 3. The human insulin gene attaches the open ends of the plasmid to form a closed ring. 4. Some bacterial cells take up the plasmids that have the insulin gene. 5. When cells reproduce, the news cells will contain copies of the engineered plasmid. The foreign gene directs the cell to produce human insulin.
When plasmids are used to produce a desired protein what happens?
When plasmids are used to produce a desired protein, the gene encoding for the protein is inserted into the plasmid. The plasmid is then introduced into a host organism, such as bacteria, which then replicate the plasmid and express the protein. This allows for large-scale production of the desired protein.
Why is ampicillin added to the pound medium?
Ampicillin is an antibiotic that is usually used as a reporter gene in cloning. A plasmid containing the ampicillin resistance gene (as well as another target gene within the plasmid) is introduced into the bacterial host. If the bacterium has taken up the plasmid and is expressing the plasmid, it will be resistant to ampicillin. LB is used as a growth medium and ampicillin to verify the plasmid is within the bactrium. No growth means no plasmid in the bacterial host...
How can one effectively clone a gene into a plasmid?
To effectively clone a gene into a plasmid, the gene of interest and the plasmid are cut with the same restriction enzymes to create compatible ends. The gene is then inserted into the plasmid using DNA ligase to seal the ends. The plasmid is then introduced into a host cell, such as bacteria, where it can replicate and express the cloned gene.
How can one effectively insert a gene into a plasmid?
To effectively insert a gene into a plasmid, one can use restriction enzymes to cut both the gene and the plasmid at specific sites. The cut gene can then be inserted into the plasmid, and DNA ligase can be used to seal the pieces together. This process is known as molecular cloning.
What is the term for a plasmid that contains a foreign gene?
Recombiant DNA
Can plasmid DNA be used for 16srRNA amplification?
The 16s rRNA genes (rDNA) exist on genomic DNA. Therefore, plasmid has nothing to do with its amplification. However, if the 16s rRNA gene is cloned into the plasmid, it can be amplified.
Which enzyme should she use to join the sticky ends of the gene and the plasmid?
She should use a DNA ligase enzyme to join the sticky ends of the gene and the plasmid. DNA ligase catalyzes the formation of phosphodiester bonds between the nucleotides of the gene and the plasmid, sealing them together.
How does a human insulin genes become part of a plasmid?
1. Scientists remove plasmids, small rings of DNA, from bacterial cells. 2. An enzyme cuts open the plasmid DNA. The same enzyme removes the human insulin gene from its chromosome. 3. The human insulin gene attaches the open ends of the plasmid to form a closed ring. 4. Some bacterial cells take up the plasmids that have the insulin gene. 5. When cells reproduce, the news cells will contain copies of the engineered plasmid. The foreign gene directs the cell to produce human insulin.
When plasmids are used to produce a desired protein what happens?
When plasmids are used to produce a desired protein, the gene encoding for the protein is inserted into the plasmid. The plasmid is then introduced into a host organism, such as bacteria, which then replicate the plasmid and express the protein. This allows for large-scale production of the desired protein.
Why is ampicillin added to the pound medium?
Ampicillin is an antibiotic that is usually used as a reporter gene in cloning. A plasmid containing the ampicillin resistance gene (as well as another target gene within the plasmid) is introduced into the bacterial host. If the bacterium has taken up the plasmid and is expressing the plasmid, it will be resistant to ampicillin. LB is used as a growth medium and ampicillin to verify the plasmid is within the bactrium. No growth means no plasmid in the bacterial host...
In the process of human gene cloning using recombinant plasmids what is the bacterial plasmid?
The bacterial plasmid is a small circular DNA molecule that is used as a vector to carry the gene of interest in gene cloning experiments. It is introduced into bacteria, where it replicates independently from the bacterial chromosome. The gene of interest is inserted into the plasmid using restriction enzymes and ligase.
When is a plasmid considered a recombinant plasmid?
A plasmid is considered recombinant when it contains DNA sequences from two different sources that have been artificially combined, often through genetic engineering techniques like restriction enzyme digestion and ligation. This results in a plasmid with modified or additional genetic material compared to its original form.
What would happen if you cut both the jellyfish glo gene and puc18 plasmid with the ecor1 restriction enzyme?
If there is a EcoR1 site in either the middle of the Glo gene, or in the middle of the selectable marker site in the plasmid, it would likely disable either Glo, or the plasmid.
Why must you use an enzyme that will not cut anywhere within the gene that you are inserting into a plasmid?
If you are trying to take a gene from a DNA strand and put insert it into a plasmid, you wouldn't want a restriction enzyme to cut that gene up, or else it would be pretty useless. In other words, you need an enzyme or two that cuts outside that gene so that it can be functional after it's inserted into a plasmid. After your gene of interest is inserted into a plasmid, the plasmid can be put back into a bacterium, then you could genetically engineer plants with it or let the bacterium reproduce and produce many copies of a protein that you had wanted to make in the first place.
