Question

why would you want your restriction enzyme to cut as close as possible to the insulin...

why would you want your restriction enzyme to cut as close as possible to the insulin gene without cutting into it?

Homework Answers

Answer #1

Q. Ans:All of this has to do with DNA conservation. If you cut the insulin gene just once, and as similar as possible to the insulin gene, you can keep the insulin gene out and very little else. Each cut has the potential to lose DNA because of wastage.

To make sure that the desired information is transferred to the plasmid without adding extra unknown or undesirable sequences. These are the reasons why restriction enzyme cut as close as possible to insulin gene without cutting onto it.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Restriction enzymes, also known as restriction endonucleases, are enzymes that cut a DNA molecule at a...
Restriction enzymes, also known as restriction endonucleases, are enzymes that cut a DNA molecule at a particular place. They are essential tools for recombinant DNA technology. The enzyme "scans" a DNA molecule, looking for a particular sequence, usually of four to six nucleotides. Once it finds this recognition sequence, it stops and cuts the strands. This is known as enzyme digestion. On double stranded DNA the recognition sequence is on both strands, but runs in opposite directions. This allows the...
How would you expect the lanes on a gel to differ if you cut the same...
How would you expect the lanes on a gel to differ if you cut the same DNA with each type of Restriction enzyme and why? (3)
Imagine you have a plasmid and you cut it with three different restriction enzymes (enzymes 1,...
Imagine you have a plasmid and you cut it with three different restriction enzymes (enzymes 1, 2, 3). You then run these fragments through a gel and get this separation. (10 pts) Label the positive and negative terminals on this gel with a (+) and (-) sign. If you were working with a single plasmid, how many cut sites did restriction enzyme 1 have? Explain? When creating a gel, we stain it with Ethidium Bromide or Gel Red. What is...
A new restriction enzyme known as Hype I recognizes the sequence GGATCC/CCTAGG. Due to random chance,...
A new restriction enzyme known as Hype I recognizes the sequence GGATCC/CCTAGG. Due to random chance, how often and what size fragments would you expect this enzyme to cut the human genome, which contains approximately 3 billion base pairs?
If you attached the gene for insulin to the gene for PDI and then express this...
If you attached the gene for insulin to the gene for PDI and then express this recombinant protein in a cell, where would you expect the insulin to end up and why? If there was no COP1 available would this have an impact on where in the cell the recombinant insulin ended up?
A specific enzyme exhibits substrate inhibition. Why would it be quite possible to increase the reaction...
A specific enzyme exhibits substrate inhibition. Why would it be quite possible to increase the reaction rate by immobilizing the enzyme in a porous spherical particle compared to using the free enzyme in solution? Explain.
1. Sickle Cell Anemia is a genetic disease caused by abnormally shaped hemoglobin in the red...
1. Sickle Cell Anemia is a genetic disease caused by abnormally shaped hemoglobin in the red blood cells. The defect is in the beta-hemoglobin gene, and the mutation is well known. In your genetic engineering lab, you plan to clone the normal sequence of the beta-hemoglobin gene into a plasmid, and then to transfer this plasmid into bacterial cells in order to make enough normal protein to pump into the blood of patients with sickle cell anemia. A partial sequence...
How would you expect the lanes on a gel to differ if you cut the same...
How would you expect the lanes on a gel to differ if you cut the same DNA with each type of enzyme and why? (3)
You are attempting to clone the human insulin gene into E.Coli so that you can have...
You are attempting to clone the human insulin gene into E.Coli so that you can have access to unlimited human insulin for medical use. Insulin is produced in pacreas, but you have human skin cells to work with. 2.) You have constructed a DNA probe, using the amino acid sequence of insulin (a short piece of DNA carrying a label, such as radioactivity, which can hybridize with your target DNA) to find your target gene. Explain whether your probe is...
1. What enzyme is used to make cDNA? restriction enzymes reverse transciptase DNA polymerase RNA polymerase...
1. What enzyme is used to make cDNA? restriction enzymes reverse transciptase DNA polymerase RNA polymerase 2. Which of the following would you NOT need to put in a test tube to do Polymerase Chain Reaction? helicase Taq polymerase nucleotides primers 3. What percentage of the human genome codes for proteins, tRNA and rRNA? 100% 1 % 0.1% 10% 4. In gene therapy what is used to get the good copy of the gene into tha patients cells? a "gene...
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT