We narrowed to 421 results for: SUA
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TypeBlog Post...between machines or the program you’re using, but usually you can click on the correct box and either manually...
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Antibodies 101: Conventional vs Spectral Flow Cytometry
TypeBlog Post...fluorescent molecules can be quite broad, detectors will usually only pick up a small portion of that spectra to... -
Of Myc and Men
TypeBlog Post...endoplasmic reticulum localization, Munro and Pelham casually introduced the Myc-tag (Munro, et al. 1986; Munro... -
Tips for a 1st time AAV user (by a Rookie AAV user)
TypeBlog Post...enough plasmid to complete my experiment. AAV is usually the limiting reagent for my experiments, so I always... -
Polymerase Chain Reaction Overview and Applications
TypeBlog Post...temperature cycling. The final PCR product is often visualized on a diagnostic agarose gel to confirm product... -
Hot Plasmids and Viral Preps - May 2021
TypeBlog Post...and more AAV1 versions will be released soon. Visualize axonal projections and putative pre-synaptic terminals... -
No Llamas Required - Synthetic Nanobodies Against Membrane Proteins
TypeBlog Post... After the ELISA step, the narrowed-down pool (usually 10-30) of sybody candidates are sequenced for identification... -
PCR Applications for Copy Number Variation Assays
TypeBlog Post...sequence present in the same amount in all samples (usually to a ubiquitously expressed, one-copy ‘housekeeping... -
The Scientific Conference Poster Session: Tips for Success
TypeBlog Post...engaging with you? Be sure to use your poster as a visual aid, not a crutch. Even the most prepared of us... -
Tips to Make the Most of a Scientific Conference
TypeBlog Post...the session, if someone comes up to my poster, I usually greet them and say something like “Let me know ... -
The AAVantages of AAV in CRISPR Screens
TypeBlog Post...infection rates in your experiment. Figure 2: Visual representation of common AAV serotypes used for... -
Plasmids 101: 5 factors to help you choose the right cloning method
TypeBlog Post...happen in a matter of minutes. Cost: Funding is usually limited - what cloning approach should you use ... -
Fluorescent Tagging of Endogenous Genes with SapTrap
TypeBlog Post...labor-intensive processes like PCR or by evaluating visual phenotypes. Improving C. elegans fluorescent protein... -
Fluorescent Proteins 101: Fluorescent Protein Timers
TypeBlog Post...predominantly fluoresce a second color. This change is usually hypothesized to be a result of chromophore oxidation... -
Plasmids 101: Knockout/Knock-In Plasmids
TypeBlog Post...gene can affect a cell's phenotype, researchers usually remove it after selection using the Cre/Lox recombination... -
Addgene's Cancer Collection Pages Connect the Research Community
TypeBlog Post...difficult to target therapeutically due to their unusually “smooth” shape and lack of “druggable” domains... -
When is a Monomer not a Monomer? The Top Three Ways Your Favorite Fluorescent Protein Oligomerizes in Cells
TypeBlog Post...proteins. One of the major applications of FPs is to visualize the localization, dynamics, and behavior of a ... -
Genome-wide Screening Using CRISPR
TypeBlog Post...error-prone non-homologous end joining (NHEJ), usually results in a loss-of-function mutation within the... -
Light Sheet Fluorescence Microscopy
TypeBlog Post...tissues transparent are enabling microscopes to visualize the cellular architecture of whole tissues in ... -
Plasmids 101: Multicistronic Vectors
TypeBlog Post...below. IRES Elements Translation in eukaryotes usually begins at the 5’ cap so that only a single translation...