We narrowed to 424 results for: SUA
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TypeBlog Post...library of transformants for single colonies (this usually requires 10-20 plates) (see box below). This initial...
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Generating Mouse Models Using CRISPR/Cas9
TypeBlog Post...oligonucleotide, we aim to generate 50 to 100 mice and are usually successful in deriving mice carrying the intended... -
Finding Your Perfect Job After University
TypeBlog Post...not suit everyone. My career path may seem quite unusual but it has allowed me to try out working in many... -
An “elegans” Approach to Better CRISPR/Cas9 Editing Efficiency
TypeBlog Post...to regulate gene expression (CRISPRi/CRISPRa), visualize specific genomic loci (CRISPR-imaging), or to ... -
A History of Genome Engineering in Popular Culture
TypeBlog Post... Genetic Engineering Era: Pre-CRISPR Having visualized and understood the DNA, the next milestone for... -
FLEx Technology and Optogenetics: Flipping the switch on gene expression with high spatial and temporal resolution
TypeBlog Post...to cell-type specific promoters; however, those usually drive weak expression of downstream genes. Strong... -
When Fidelity Matters: A frank discussion about ligase fidelity
TypeBlog Post...differences. The original creators of this technique visualized the ligation product in a gel, but we can now... -
Transferable Skills Guide: Teamwork
TypeBlog Post...experiments I’d been learning about for years were usually the products of teams: Watson, Crick, & Franklin... -
Quick Guide to All Things Lentivirus
TypeBlog Post... will first need to transfect producing cells, usually 293T cells, with your transfer plasmid and your... -
Tips for a 1st Time CRISPR User (by a 1st Time CRISPR User)
TypeBlog Post... digestion products (which could be easier to visualize and identify). If you need/want to put the digestion... -
A Guide to Getting Started in Undergrad Research
TypeBlog Post...and responsibilities can vary "Lab assistants" usually wash glassware, prep media, etc. "Research assistants... -
Sequencing Options for CRISPR Genotyping
TypeBlog Post...mismatches and cleave them. The results are then visualized using gel electrophoresis. Surveyor™ and T7E1... -
Custom CRISPR Screens & the Green Listed Software
TypeBlog Post...available from commercial vendors. These libraries usually contain 4-12 gRNAs/gene, which results in libraries... -
Typing CRISPR Systems
TypeBlog Post...effectors, like Cas9. The Cascade complex doesn’t usually carry out the function of the specific CRISPR type... -
Plasmids 101: Modular Cloning Applications and Kits
TypeBlog Post...chromosomal integration modules, and many more of the usual suspects. The Multiplex Yeast Toolkit builds on ... -
With an Eye Towards the Future, We Look Back at the March for Science
TypeBlog Post...not be partisan: everyone (of every political persuasion) must be humble in the face of evidence. Stephanie... -
Special Delivery: Fluorophore Targeting for FRET Studies
TypeBlog Post...antigen interactions (Saraheimo et al., 2013), and visualizing structural changes in the ribosome during protein... -
CRISPR 101: Multiplex Expression of gRNAs
TypeBlog Post...system, editing or labeling efficiency doesn’t usually change when you add multiple gRNAs on one plasmid... -
CRISPR 101: Cytosine Transversion Editors
TypeBlog Post...this “non-target strand.” To avoid confusion, we usually use different terminology when discussing base ... -
Promoters
TypeGuide...functionally equivalent called the Pribnow box which usually consists of the six nucleotides, TATAAT. Proximal... span a wide range of DNA sequences. It is not unusual to have several regulatory elements such as enhancers...