We narrowed to 718 results for: STO
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TypeBlog Post...genetics and anatomy, which are not yet fully understood. We attempt to deconstruct and understand this... into it! If you’re in the Victoria area, please stop by. And if not, I suspect you can find a makerspace...
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7 Simple Strategies to Resolve Conflicts with Difficult Supervisors
TypeBlog Post... 5) Listen to your supervisor’s viewpoint and brainstorm about mutually beneficial solutions Your supervisor...Look at the problem from their viewpoint, and brainstorm about solutions that will meet both of your needs... -
Degrading DNA with Cascade-Cas3
TypeBlog Post... cleaving of the target strand is not as well understood but likely occurs in similar regions. This combination...up to hundreds or even thousands of base pairs, stopping either at boundaries defined by anti-CRISPR proteins... -
Production of Virus in Insect Versus Mammalian Cells
TypeBlog Post...particles you need are not available, or the cost of custom viruses are too high for your budget. In those ...round provides the added benefit of producing a stock P1 virus, so that if you ever need to remake the... -
Plasmids 101: 5 factors to help you choose the right cloning method
TypeBlog Post...restriction sites allowing you to easily create customized overhangs to assemble up to 6 different fragments...PCR process (the precise mechanism isn’t well understood). Finally, TOPO cloning is another good option... -
xCas9: Engineering a CRISPR Variant with PAM Flexibility
TypeBlog Post...-3.13. To test xCas9 3.0-3.13, Hu et al. first restored catalytic residues D10 and H840. To ensure that...Plasmids for Mammalian Systems Learn about CRISPR History ... -
Fluorescent Proteins 101: Visualizing Subcellular Structures & Organelles
TypeBlog Post...see our plasmid collection from Sue Jaspersen (Stowers Institute) and Mark Prescott (Monash University...ImageJ plugins JACoP and Coloc 2, BioImageXD, and customized CellProfiler pipelines. Image analysis software... -
The Scientific Conference Poster Session: Tips for Success
TypeBlog Post...to tailor your presentation so that it can be understood by your audience. Use your poster as an aid: ... practicing with your colleagues, ask them to brainstorm potential questions you may receive. People often... -
CrispyCrunch: High-throughput Design and Analysis of CRISPR+HDR Experiments
TypeBlog Post...HDR. If the max CFD score is less than 0.03, it stops mutating. (This happens often because the HDR inserted...will check the CFD score. If it is below 0.03, it stops mutating. (Note: the most common synonym in the ... -
No Llamas Required - Synthetic Nanobodies Against Membrane Proteins
TypeBlog Post...Each mRNA molecule in the library doesn’t encode a stop codon, which causes the ribosome to pause at the... Zimmermann I, Egloff P, Hutter CA, Arnold FM, Stohler P, Bocquet N, Hug MN, Huber S, Siegrist M, Hetemann... -
Polymerase Chain Reaction Overview and Applications
TypeBlog Post...late 1960s during research at hot springs in Yellowstone National Park. In addition to Taq DNA polymerase... low during the final cycles which would slow or stop PCR amplification. Other times, the PCR reaction... -
Chromoproteins: Colorful Proteins For Molecular Biology Experiments
TypeBlog Post...levels. Chromoproteins in nature Compared to the history of fluorescent proteins in molecular biology research...research, chromoproteins have a shorter history. In 1987, scientists described an unusual blue-colored... -
3D Printing Meets CRISPR Cas9
TypeBlog Post...resulted from our work with teachers, and to create custom models of proteins for researchers. Modeling CRISPR...Addgene.org Visit Our CRISPR Guide Page CRISPR/Cas9 History Browse All CRISPR Plasmids and Resources ... -
Plasmids 101: Optimizing Plasmid Yields
TypeBlog Post... like PCR, cloning, transfection, or long-term storage. But what about those pesky situations where your...colony Sub-culturing directly from a frozen glycerol stock or agar stab may lead to loss of the plasmid, and... -
When is a Monomer not a Monomer? The Top Three Ways Your Favorite Fluorescent Protein Oligomerizes in Cells
TypeBlog Post... was contributed by guest blogger Erik L. Snapp. Stop using EGFP/GFP for fusion proteins! Despite multiple...spiderweb-like pattern of tubules can be grossly distorted into dense stacked membranes termed Organized ... -
PITChing MMEJ as an Alternative Route for Gene Editing
TypeBlog Post... cassette into a given locus, just upstream of a stop codon. Briefly, the PITCh vector should be constructed...the GFP-Puro will be inserted just upstream of a stop codon. One potential concern is if the GFP-Puro ... -
Anatomy of a Plasmid Page at Addgene
TypeBlog Post...would be useful for their own research, and helps requestors use the plasmid in their own labs. We highly ...survival (for Gateway plasmids). We also like to store plasmids that need extra stability, such as some... -
Light Sheet Fluorescence Microscopy
TypeBlog Post...that also allows antibody penetration for immunohistochemical labeling in whole tissue (15). CLARITY is...236. Pubmed. P.A Santi. (2011). Journal of Histochemistry & Cytochemistry, 59, 129-138. Pubmed. J. Huisken... -
Plasmids 101: Multicistronic Vectors
TypeBlog Post...use the 2A peptides instead of an IRES when stoichiometrically equivalent levels of expression are required...Addgene's new eBook! Our goal was to create a one-stop reference guide for plasmids. We've combined our... -
What’s in Your Tube?: A Quick Guide to Measuring DNA by Spectrophotometry
TypeBlog Post...molecules can alter the overall 260 nm reading, distorting the final concentration calculation and potentially...Different Uses What's the Best Way to Elute and Store Your Plasmid DNA? Selecting Your Plasmid Purification...