We narrowed to 276 results for: ATC
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TypeBlog PostPublishedMay 24, 2018, 1:20 p.m....unrelated worm (C. elegans) [2]. Delivering dsRNA matching a specific mRNA sequence triggers a cascade of...
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Hot Plasmids May 2018 - Optogenetics, Decaffeination, Biosensors, and Fluorescent Protein Tools
TypeBlog PostPublishedMay 15, 2018, 12:43 p.m....neighboring cells evokes action potentials (APs) in patched cells expressing wild type CoChR, these APs are... -
CRISPR 101: Anti-CRISPR Proteins Switch Off CRISPR-Cas Systems
TypeBlog PostPublishedJuly 23, 2020, 1:20 p.m....light-inducible Cas9 activity? Check out these these plasmids Catch Up on Your CRISPR Background with Our Guide Pages... -
Plasmids 101: The Wide World of Natural Plasmids
TypeBlog PostPublishedOct. 8, 2024, 1:15 p.m....Cryptic plasmids: microbial mysteries Cryptid hunters watch out — cryptic plasmids are real! This term refers... -
Plasmids 101: Modular Cloning
TypeBlog PostPublishedMarch 12, 2024, 1:15 p.m....Interested in using MoClo? You don’t have to start from scratch! As you can imagine, there is an array of distinct... -
Split Fluorescent Proteins for Studying Protein-Protein Interactions
TypeBlog PostPublishedMay 3, 2022, 1:15 p.m.... available, with many ways to split and mix and match them, so where should you begin? Have no fear, Addgene... -
Viral Vectors 101: Calcium Sensors
TypeBlog PostPublishedAug. 10, 2023, 1 p.m....with a little nuance discussed below, will help match your experiment with a sensor that is tuned to your... -
High Complexity Golden Gate Assembly with NEB’s DAD
TypeBlog PostPublishedAug. 1, 2023, 1:15 p.m.... identify overhangs with a high potential for mismatches, so you can redesign individual pieces as needed... -
How-to: 5 Steps to a Great Panel Discussion
TypeBlog PostPublishedOct. 22, 2014, 1:57 p.m....are at a talk and the speaker goes over 1 hour, watch what happens to the attention of the audience – ... -
Fluorescent Proteins 101: Fluorescent Protein Timers
TypeBlog PostPublishedMay 4, 2017, 2:30 p.m....Learn More About Fluorescent Protein Aggregation Catch Up On Your GFP Basics Get Advice on Choosing Your... -
Truncated gRNAs for Regulating Gene Expression
TypeBlog PostPublishedJan. 10, 2017, 3:37 p.m....largely been demonstrated to result in decreased mismatch tolerance and, consequently, increased specificity... -
xCas9: Engineering a CRISPR Variant with PAM Flexibility
TypeBlog PostPublishedMarch 28, 2018, 6:52 p.m.... of xCas9 3.6 and 3.7 shows that we have only scratched the surface of modifications that can be made ... -
The Scientific Conference Poster Session: Tips for Success
TypeBlog PostPublishedAug. 29, 2019, 12:50 p.m....but will also give you a chance to slow down and catch your breath before diving in to the next figure.... -
PRIDICT: Predicting Efficiencies of Prime Editing Guide RNAs
TypeBlog PostPublishedJune 25, 2024, 1:15 p.m....offline use via GitHub (which includes prediction in batch mode). To predict the best pegRNA design for a specific... -
Transferable Skills: Negotiation
TypeBlog PostPublishedMarch 3, 2022, 2 p.m....Resources on Addgene.org Check out our careers page Watch our career videos ... -
Degrading DNA with Cascade-Cas3
TypeBlog PostPublishedFeb. 11, 2025, 2:15 p.m....of DNA much like a fisherman would reel in a big catch. It was originally suspected that Cas3 moved a couple... -
The AAVantages of AAV in CRISPR Screens
TypeBlog PostPublishedFeb. 4, 2025, 2:15 p.m....Customization AAV offers a level of customization that is unmatched by other viral vector delivery methods. Lentivirus... -
Google Forums Round Up: First Impressions of NgAgo
TypeBlog PostPublishedAug. 4, 2016, 2:30 p.m....Addgene.org Request NgAgo Find CRISPR Resources Catch Up on Your CRISPR Background ... -
Experimenting with New Careers while in Grad School
TypeBlog PostPublishedFeb. 25, 2016, 3:30 p.m....easily share science with the public, but I can watch and learn from the experts in science communication... -
CRISPR 101: Mammalian Expression Systems and Delivery Methods
TypeBlog PostPublishedSept. 24, 2015, 2:30 p.m.... you be detecting insertions/deletions using a mismatch repair assay? Or is PCR followed by gel electrophoresis...