CRISPR genetic editing methods in target diseases
CRISPR genetic editing methods in target diseases, available at $44.99, has an average rating of 4.56, with 6 lectures, based on 8 reviews, and has 99 subscribers.
You will learn about You will learn genetic treatment methods in target diseases with CRISPR-Cas approaches. Design CRISPR Cas project Design guide RNA, Decision of best Cas system Base editing, Prime Editing, Transposase and Knockout systems This course is ideal for individuals who are Medicine, Molecular Biology and Genetics and Biology departments It is particularly useful for Medicine, Molecular Biology and Genetics and Biology departments.
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Summary
Title: CRISPR genetic editing methods in target diseases
Price: $44.99
Average Rating: 4.56
Number of Lectures: 6
Number of Published Lectures: 6
Number of Curriculum Items: 6
Number of Published Curriculum Objects: 6
Original Price: $24.99
Quality Status: approved
Status: Live
What You Will Learn
- You will learn genetic treatment methods in target diseases with CRISPR-Cas approaches.
- Design CRISPR Cas project
- Design guide RNA, Decision of best Cas system
- Base editing, Prime Editing, Transposase and Knockout systems
Who Should Attend
- Medicine, Molecular Biology and Genetics and Biology departments
Target Audiences
- Medicine, Molecular Biology and Genetics and Biology departments
The CRISPR revolution has begun and shows no signs of slowing down. This system, which is the key to prokaryotic adaptive immunity, has proven to be particularly under the influence of genome engineering. CRISPR/Cas provides flexibility as well as easily amplifying the signal and regulating the signal level, which is beyond the capabilities of previous systems. Prokaryotes have long exploited CRISPR/Cas as a powerful defense strategy against virus-derived invaders, and eventually, this system turns out to be useful only for research applications.
Just when we thought that genome engineering could not get any further, the CRISPR (clustered regularly spaced short palindromic repeats)/Cas9 system emerged. It is an important component of the bacterial immune system, allowing bacteria to recognize and destroy phages. In genome engineering applications, guide RNA (gRNA) sequence homology targets the Cas9 endonuclease to a specific locus—where the double helix is broken. Like ZFNs and TALENs, CRISPR/Cas9 uses HDR, but using RNA to determine editing makes the system more sensitive and malleable, as well as less expensive and time-consuming. For this reason, CRISPR/Cas9 has proven invaluable for high-throughput genome engineering.
With a variety of robust and effective genome engineering methods at our fingertips, we have entered the Golden Age of genome engineering. Current studies have focused on developing these techniques in the hope that they will be clinically useful to provide desired target loci (or loci), high specificity, and efficacy. The most exciting thing we’ve found at Addgene is the democratization of genome engineering that has enabled and will continue to enable researchers around the world to use these tools. To learn all about CRISPR, you must complete the course.
CRISPR/Cas Gene Editing Training Program
i. What is CRISPR-Cas?
ii. What are CRISPR-Cas Systems?
iii. CRISPR Genetic Therapy Applications
iv. Planning Your CRISPR Project
v. Guide RNA Design & Benchling
vi. Confirmation of your Gene Editing
Course Curriculum
Chapter 1: Introduction: What is CRISPR/Cas?
Lecture 1: Introduction: What is CRISPR/Cas?
Chapter 2: Chapter 2: What are CRISPR/Cas Systems?
Lecture 1: chapter 2
Lecture 2: chapter 2 continue
Chapter 3: chapter 3: CRISPR/Cas Genetic Therapy Applications
Lecture 1: chapter 3
Chapter 4: chapter 4: Designing a CRISPR/Cas Gene Editing Project
Lecture 1: chapter 4
Chapter 5: chapter 5: CRISPR/Cas Gene Editing Confirmation Methods
Lecture 1: chapter 5
Instructors
-
Cihan Taştan
Dr. Öğr. Üyesi
Rating Distribution
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- 2 stars: 0 votes
- 3 stars: 1 votes
- 4 stars: 3 votes
- 5 stars: 4 votes
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