Question

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)

Homework Answers

Answer #1

If we cut the DNA with different types of type 2 restriction enzymes then the corresponding bands on the various lanes will differ according to there molecular sizes and also in the total number of bands present on lane. The main reason for this observation is that different restriction enzyme will cut according to their recognition sites which differ from enzyme to enzyme and also different number of bands will be due to the frequency of the recognition sites that come on DNA of that particular emzyme.

Also the different recognition enzymes like type 1 type 2 and type 3 etc will differ on there gel profile based on how near they cut the DNA to the site they recognise i.e. whether they cut same DNA sequence which they recognise.

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
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)
2) Answer the following questions: What is the size of the lambda DNA? What is the...
2) Answer the following questions: What is the size of the lambda DNA? What is the recognition sequence recognized by HindIII? How many times will the enzyme cut the lambda DNA? What is the driving force that propels the DNA though the gel? Where should the positive electrode be positioned related to the gel? Using the gel in the virtual lab. If the lanes are numbered 1-4 (from left to right), which lane contains uncut DNA? How do you know...
You’ve been asked to prepare the gel. How much agarose would you need to weigh in...
You’ve been asked to prepare the gel. How much agarose would you need to weigh in order to prepare 50 ml of 2% gel? Show your math. List three things to which one needs to pay special attention when loading a gel for DNA electrophoresis. What would be the volume of the PCR sample you would have loaded in live lab? The loading buffer has a dual purpose. Explain. There are multiple reasons for loading a DNA ladder (size standard)...
What would you expect to differ and remain the same between a protein isolated from different...
What would you expect to differ and remain the same between a protein isolated from different species? To answer this question, please consider both the primary sequence and the tertiary structure of the protein. So would the primary sequence and tertiary structure stay the same or be different in a protein isolated from different species?
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...
How would you expect the elasticity of supply of product X to differ in a situation...
How would you expect the elasticity of supply of product X to differ in a situation of full employment in Industry X on the one hand, and of considerable unemployment in the industry on the other hand?
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 EI and CI mass spectra of stearyl amine (MW=269) to differ?...
How would you expect the EI and CI mass spectra of stearyl amine (MW=269) to differ? If the CI mass spectrum is collected using methane as a reagent gas, would you expect to see any peaks in the spectrum at m/z > 269? Explain.
On an infrared spectrum, how would norandrosterone and nandrolone differ? How would they appear the same?
On an infrared spectrum, how would norandrosterone and nandrolone differ? How would they appear the same?
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?
ADVERTISEMENT
Need Online Homework Help?

Get Answers For Free
Most questions answered within 1 hours.

Ask a Question
ADVERTISEMENT