We narrowed to 219 results for: ttl
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TypeBlog PostPublishedSept. 14, 2016, 2:30 p.m....you can create custom RNA binding proteins in as little as 3 days. Abil et al., 2014 show that you can ...
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10 Steps to a Perfect Science Talk
TypeBlog PostPublishedAug. 23, 2016, 2:30 p.m....learn new things, so rehash common knowledge as little as possible. Don’t use a lot of jargon in your ... -
Targeting HIV-1 with CRISPR: Shock and Kill or Cut it Out?
TypeBlog PostPublishedMay 10, 2016, 2:30 p.m....evade immune detection because they produce very little or no viral protein. To solve this problem, two... -
Treating Muscular Dystrophy with CRISPR Gene Editing
TypeBlog PostPublishedJan. 26, 2016, 3:30 p.m....joining (NHEJ) pathway. It’s estimated that very little dystrophin correction (about 4%) is needed to see... -
Plasmids 101: Common Lab E. coli Strains
TypeBlog PostPublishedNov. 7, 2014, 2:56 p.m....work! But let’s take a moment to recognize your little prokaryotic minions that carried out the labor-... -
Is this the right place for me? 8 tactics for choosing a lab
TypeBlog PostPublishedOct. 2, 2018, 12:56 p.m....? Threats to professional status – including belittling opinions, public professional humiliation, accusations... -
How to Design Your gRNA for CRISPR Genome Editing
TypeBlog PostPublishedSept. 24, 2020, 1:15 p.m....importance in design – an optimized sequence will do little if it is in the wrong place, but because the target... -
Viral Vectors 101: Optogenetic Tools
TypeBlog PostPublishedJune 27, 2023, 1:15 p.m....range of wavelengths. While this may give you a little flexibility when activating the optogenetic tool... -
Recombinase-based State Machines Enable Order-dependent Logic in vivo
TypeBlog PostPublishedJuly 28, 2016, 2:30 p.m....conditions drive certain cellular behaviors, but little is known about the order or timing of these factors... -
Plasmids 101: Restriction Cloning
TypeBlog PostPublishedFeb. 18, 2016, 3:42 p.m....enzymes that can digest large amounts of DNA in as little as 10 minutes, but check with your enzyme’s manufacturer... -
Finding Your Perfect Job After University
TypeBlog PostPublishedJan. 12, 2016, 3:30 p.m.... and working at the bench, but the reality is a little different. Industry and academic jobs do exist,... -
Quick Guide to All Things Lentivirus
TypeBlog PostPublishedMarch 21, 2017, 2:30 p.m....difficult to interpret your results. This can be a bottleneck for your experiment. Single vector systems containing... -
Tips for a 1st Time CRISPR User (by a 1st Time CRISPR User)
TypeBlog PostPublishedMarch 7, 2017, 3:30 p.m....We all know that in the lab there are often little tricks that are essential for experiments but that... -
Antibodies 101: Validation
TypeBlog PostPublishedMarch 24, 2022, 1:15 p.m....strong antibody signal in the retinal sample, but little to no signal in the liver sample, which you do ... -
Fluorescent Proteins 101: Monitoring Cell Mobility Using Fluorescent Proteins
TypeBlog PostPublishedAug. 15, 2017, 1:24 p.m....,000 nm and 1,200 nm, where there is relatively little tissue absorption, weak tissue scattering and small... -
Fluorescent Proteins 101: Photoactivatable Fluorescent Proteins
TypeBlog PostPublishedApril 25, 2017, 2:30 p.m....Atsushi Miyawaki. "Regulated fast nucleocytoplasmic shuttling observed by reversible protein highlighting." ... -
Plasmids 101: Modular Cloning Applications and Kits
TypeBlog PostPublishedMay 14, 2024, 1:15 p.m....Parts II kit has a focus on infrastructure with shuttle vectors, several delivery systems which can be ... -
27 Hot Plasmids from 2016
TypeBlog PostPublishedDec. 22, 2016, 3:03 p.m....PRESTO-TANGO kit directly for drug screening or easily shuttle the optimized, expression validated GPCR sequences... -
28 Hot Plasmid Technologies from 2015
TypeBlog PostPublishedDec. 23, 2015, 3:30 p.m....treatment, the Cas9(N)-FRB-NES fragment is actively shuttled out of the nucleus due to the nuclear export sequence...