15. The CRISPR/Cas9 system provides a form of adaptive immunity in bacteria. We discussed in class that it can be used in human cells to: A: Protect cells from infection with viruses B: Kill cells that carry a specific deletion C: Give cells a memory of the viruses that have infected them D: Greatly enhance the frequency of homologous recombination at a chosen I locus E: Kill cells that have not undergone the desired genome edit

15. The CRISPR/Cas9 system provides a form of adaptive immunity in bacteria. We discussed in class that it can be used in human cells to: A: Protect cells from infection with viruses B: Kill cells that carry a specific deletion C: Give cells a memory of the viruses that have infected them D: Greatly enhance the frequency of homologous recombination at a chosen I locus E: Kill cells that have not undergone the desired genome edit

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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Similar questions

i) Suppose we want to insert the GFP sequence after the promoter of a gene X to create a fusion protein. Please describe the strategy that you will follow to edit this gene with CRISPR-Cas9 technology, in order to visualize the expression of gene X in live cells. (ii) Please explain how a knockout mouse for a gene X can be produced with CRISPR-Cas9 technology
58. (more than one correct answer)
1 and/or 2 please
Where did the Crispr system first originate and what is its purpose in nature? What is the advantage to using the CRISPR-Cas9 system compared to previous gene editing technologies? What are the advantages? Any drawbacks? What are the ethicals concerns that are raised with the use and application of this technology? What do you think of this technology?
CRISPR-Cas9 can be used by scientists to edit genes. This system was not created in a lab, however, but instead adapted from a system that already exists in nature. Describe the native biological function of CRISPR-Cas9.
Genetically modified Atlantic salmon have recently been approved for human consumption. These genetically modified Atlantic salmon have a growth hormone gene from the Chinook salmon which allows them to grow to market size in double the time. This was possible because of CRISPR/Cas9 technology. From what you know about gene editing and CRISPR/Cas9, name 2 components of the technology that had to be introduced into the Atlantic salmon. Which method of DNA repair had to be used (non-homologous end joining or homology‐directed repair) to edit the Atlantic salmon genome?
CRISPR/Cas9 mediated genome editing has provided an unparalleled means of manipulating the genome. Describe in 2 sentences/lines maximum what three requirements must be met in order to target a specific dsDNA break at a given site in genome of the target organism using this system?
8) Draw a two-stranded, antiparallel ß-sheet with at least four amino acids in each B-strand.
What is the function of gRNA in CRISPR-Cas technologies?It cuts DNA at a targeted sequence and inserts a new sequence -.It cuts protein at a targeted sequence and inserts a new sequence.It ensures the Cas9 enzyme cuts at the correct place in the DNA.It ensures the Cas9 enzyme cuts at the correct place in the RNA.It replaces uracil nucleotides with thymine nucleotides.
How does one perform a Southern blot and how does one performs a western blot. What can a Southern blot can detect, and what can a western blot can detect. Connect a specific biological mechanism for how viruses can cause cancer to each of the two pieces of data that you have.
A large molecule of DNA containing genes essential for the survival of an organism is called a/an Plasmid MRNA Operon Chromosome MacBook Air DII DD 80 000 000 F9 F8 F7 F6 F4 F5 F3 & $4 8.
1) Using the diagram below, sketch in the pattern of bands you would expect to see after digesting the DNA of the TT, Tt and tt genotypes of the TAS2R38 gene. Use the Base Pair Standards on the left of the diagram as a reference in drawing the positions of the bands. Base Pair TASTER GENO TYPE Standards (Base Pairs) TT Tt tt 500 400 300 200 100 50