Question

You are studying a human protein, XYZ, that localizes to the nucleus in human cells. You want to see if it will also localize
0 0
Add a comment Improve this question Transcribed image text
Answer #1

Answere :-

Correct option is "only mouse"

Explanation :- aim of given experiment is to study the human protein XYZ , whether it localises in mouse nucleus as it localises in human cells.

For that we fused this protein with jellyfish flueroscent protein -GFP.

Then we put it to plasmid , where it translated as a single protein (this step occured outside the human and jellyfish cells).

This plasmid is then inserted to E.coli to obtain more plasmid.

(Plasmid is a self replicating organelle therefore Ecoli doesn't required a promoter driving given fused gene)

It is then harvested,and by using crisper /cas9 technology to trick homologous recombination into copying this fused gene into a defined site in the mouse gene.(here mouse cell required the promoter driving XYZ-GFP gene ).

Add a comment
Know the answer?
Add Answer to:
You are studying a human protein, XYZ, that localizes to the nucleus in human cells. You...
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. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • In a separate line of experiments, you are studying a protein that you suspect shuttles between...

    In a separate line of experiments, you are studying a protein that you suspect shuttles between the nucleus and the cytoplasm. However, when you localize a GFP-tagged fusion protein, it appears to be only in the nucleus. To test whether it shuttles, you set up a heterokaryon assay. You take a cell expressing the GFP fusion protein and partially fuse that cell with another that does not express the GFP protein. The result is a heterokaryon that has a single...

  • You wish to edit a gene in a population of stem cells using CRISPR/Cas9. You design...

    You wish to edit a gene in a population of stem cells using CRISPR/Cas9. You design a plasmid and transfect it into the cells. Your plasmid included the guide RNA sequence with promoter, the Cas9 gene inserted between an appropriate promoter and termination sequence, and the usual Origin of Replication and Resistance/Marker gene. However, instead of being edited, your target gene is silenced and its protein is not produced at all. What is the most likely explanation? The cells have...

  • the genetic blueprint of an organism is referred to as i A scientist wishes to genetically...

    the genetic blueprint of an organism is referred to as i A scientist wishes to genetically engineer E. coli bacteria so that it will contain the green fluorescent protein (GFP) gene. Which of the following protocol outlines would the scientist use to accomplish this task? ОА Insert GFP gene into corn expression cassette; insert expression cassette into plasmid vector; insert plasmid vector into Agrobacterium tumefaciens bacteria; allow bacteria to infect corn plant; GFP gene inserted into com cell genome. ....

  • You have designed a CRISPR/Cas9 plasmid and have successfully transfected it into human cells. However, when...

    You have designed a CRISPR/Cas9 plasmid and have successfully transfected it into human cells. However, when you sequence the genome of these cells a week later, it appears that the cuts were made in the wrong location, silencing the wrong genes. This is most likely due to a problem with... the guide RNA O Cas9 the Shine-Dalgarno sequence on the plasmid O the Cas9 promoter on the plasmid the transfection procedure O

  • Fluorescent Protein Gene Fusia for Subcellular Localization Imaging 5. (2 pts) You are studying the human...

    Fluorescent Protein Gene Fusia for Subcellular Localization Imaging 5. (2 pts) You are studying the human alpha tubulin protein (which is a part of microtubules). You fuse the protein to a GFP in order to observe it. a. Why would you want to attach a GFP to tubulin (what kind of info would it show you) and why would you prefer this method to using a stain that binds to tubulin? 26 Humana EOFI Se Termine A Acid Figure 4...

  • Protein P is synthesized in relatively high amounts in the human pancreas. This protein has been...

    Protein P is synthesized in relatively high amounts in the human pancreas. This protein has been isolated and purified, but its amino acid sequence has not been determined. We wish to clone the gene for protein P. (a) How can a probe be prepared to identify the gene for protein P? (b) If we have prepared a radioactive messenger RNA as our probe in part (a), how could we verify that it is the mRNA for protein P? (c) If...

  • You are studying a human mRNA that you believe is controlled at the level of translation....

    You are studying a human mRNA that you believe is controlled at the level of translation. You think that the 5’-UTR plays a role by binding to a protein that prevents the initiation of translation. To definitively determine the role of the 5’-UTR, you decide to clone the 5’UTR of the gene upstream of GFP open reading frame in a mammalian expression vector. Question: Describe an experiment that you would perform using this vector to prove that the 5’ UTR...

  • A. You want to make a translational fusion of protein Z and the yellow fluorescent protein...

    A. You want to make a translational fusion of protein Z and the yellow fluorescent protein YFP (Z-YFP) so that expression of the fusion occurs with the same cell-specific pattern as that of protein Z. The protein Z gene has a 2 kb promoter, two 1 kb exons, and one 5 kb intron. The YFP gene is 0.7 kb. Outline with words and sketches your strategy to make the Z-YFP fusion clone using PCR. You already have cells that contain...

  • molecular biology Section C (40 marks) Answer ALL questions from this Section 5. You have isolated total RNA from muscle cells and constructeda muscle cDNA library. You wish to study the regulatory r...

    molecular biology Section C (40 marks) Answer ALL questions from this Section 5. You have isolated total RNA from muscle cells and constructeda muscle cDNA library. You wish to study the regulatory region of a muscle-specific cDNA gene (gene M) that you have previously identified. 6 (a) For your study, you need to isolate a genomic clone of gene M. Why isa cDNA clone of gene M not appropriate for your study? (2 marks) (b) Outline the steps you would...

  • 3. EML is a protein that is produced at low levels in healthy cells, but is...

    3. EML is a protein that is produced at low levels in healthy cells, but is highly expressed in cancer cells. You know that EML expression correlates with HER2 activity in cancer cells, but you do not know if EML causes HER2 activation or if HER2 activation induces EML expression. a. Your PI thinks that it would be a good idea to look into quantifying expression of EML. What method would you use? b. The particular method you most likely...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT