We narrowed to 743 results for: UTY;
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TypeBlog Post...laundry list of molecules to screen has unclear utility. You cannot predict what will happen. Without the...
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Controlling for Off-target Effects with a New Genome-wide CRISPR Screen Design
TypeBlog Post...and its subsequent repair. Additionally, the distribution of enrichment and depletion scores for safe-... -
Transferable Skills Guide: External Collaborations
TypeBlog Post...minutes. Get to know your collaborators from other institutions personally on conference calls and make sure... -
How to Write a Scientific Review Article
TypeBlog Post...t have to be long and it doesn’t have to be revolutionary, but you could include a few comments on where... -
5 Reasons to Use Reddit for Science Communication
TypeBlog Post...Addgene Executive director, Joanne Kamens, recently participated in a Reddit AMA (short for “Ask Me Anything... -
Important Considerations in Optogenetics Behavioral Experiments
TypeBlog Post...experiments. There are far too many behaviors that have utilized optogenetics to be fully summarized in a short... -
Plasmids 101: E. coli Strains for Protein Expression
TypeBlog Post...? As mentioned above, many expression plasmids utilize inducible promoters, which are 'inactive' until... -
Transfection for Recombinant Antibodies
TypeProtocol...ensure that you are in compliance with your institution’s biosafety regulations. Last Update: February...Leupeptin, Millipore Sigma L2884 Aprotinin saline solution, Millipore Sigma A6279 Before Starting Warm the...µm filter. Prepare 10 mL aliquots and store the solution at -20 °C. 1 mg/mL PEI-MAX Add 1 g of PEI-MAX ...but check for the presence of particles still in solution. Continue to stir until all particles have dissolved... to ensure that it has not drifted. Filter the solution through a 0.22 µm filter. Prepare aliquots and...at 4 °C until use. We suggest preparing fresh solutions after one month. BCD Feed 500 mL BalanCD HEK293...at 4 °C until use. We suggest preparing fresh solutions after one month. 1000X protease inhibitor cocktail... -
Protocol - pLKO.1 – TRC Cloning Vector
TypeProtocol...must contact your institution’s Bio-Safety office to receive permission and institution-specific instructions...sulfate for polybrene. c. Add lentiviral particle solution from step E. For a 6 cm target plate, add between...Please follow all safety guidelines from your institution and from the CDC and NIH for work in a BL2 facility...safety practice to follow, please contact your institution’s safety office. For more information, please ...extract 10g sodium chloride 15g agar Prepare LB agar solution by dissolving 40g of LB powder in 1L of distilled...Hexadimethrine Bromide (Polybrene) Prepare a 1mg/mL solution of polybrene (Sigma-Aldrich catalog #H9268) in...in 0.9% NaCl. Autoclave to sterilize. Stock solution is stable at 4°C for up to one year. The powder form... -
CRISPR Library Amplification
TypeProtocol...cuvette. Pulse. Caution Electroporation involves the use of high voltages, please use caution when activating... a second and then third 1:100 dilution). Plate 100 µL of each dilution onto a prewarmed Petri dish. Incubate...adequate time to fully gel and to dry slightly. We routinely use 350 mL of LB Agar per bioassay plate. 14 mL... mix the four tubes. Perform sequential 1:100 dilutions of the cells (add 10 µL of the pool to 990 µL ... colonies can be too great to count. Ideally, dilutions would have been sufficient to enumerate single...plate, count the second plate (ie. the 1:10,000 dilution). After 12-18 hours of growth, use spreader and...suspended in cryoprotectant like Glycerol or DMSO solutions. Quantify the individual Maxipreps by Nanodrop... -
Antibodies 101: Introduction to Immunofluorescence
TypeBlog Post...protocol, multiplex IF can give you impactful and beautiful results. Performing an immunofluorescence experiment... -
Fluorescent Proteins 101: GFP Fusion Proteins - Making the Right Connection
TypeBlog Post...considered when interpreting results. The recent revolution in genome editing methods (most notably CRISPR... -
Deep Mutational Scanning with One Pot Saturation Mutagenesis
TypeBlog Post...strand. Each degenerate primer set contains three consecutive randomized bases (NNN) at a given codon site ... -
CRISPR 101: Engineering the Plant Genome Using CRISPR/Cas9
TypeBlog Post...engineering world by storm owing to its ease of use and utility in a wide variety of organisms. While much of ... -
Hot Biosensors 2022: Year-End Roundup
TypeBlog Post...local temperature sensing with sub-millisecond resolution and sub-degree temperature differences under ... -
An Integrin Antibody Toolkit from IPI
TypeBlog Post...Addgene to accelerate biomedical research by distributing antibodies developed by IPI. Our integrin antibodies... -
General Transfection
TypeProtocol...hydrochloric acid until the solution clears. Check the pH of the solution Use hydrochloric acid or sodium...hydroxide to adjust the pH to 7.0. Typically, the solution will be basic and will need adjustment with hydrochloric...hydrochloric acid first. Pro-Tip The pH of this solution will drift pretty rapidly upon addition of acid...over or undershooting the desired pH. Allow the solution to mix for 10 min and then recheck the pH to ensure... ensure that it has not drifted. Filter the solution through a 0.22 µm membrane. Aliquot 500–1000 µL into.... Store the tubes at -80 °C. After thawing the solution can be stored at 4 °C for up to 2 months. After... -
Lentivirus Production
TypeProtocol...hydrochloric acid until the solution clears. Check the pH of the solution. Use hydrochloric acid or sodium...hydroxide to adjust the pH to 7.0. Typically, the solution will be basic and will need adjustment with hydrochloric...hydrochloric acid first. Pro-Tip The pH of this solution will drift rapidly upon addition of acid or base...over or undershooting the desired pH. Allow the solution to mix for 10 min and then recheck the pH to ensure... ensure that it has not drifted. Filter the solution through a 0.22 μm membrane. Aliquot 500–1000 μL into... tubes at -20 °C or -80 °C. After thawing, the solution can be stored at 4 °C for up to 2 months. After... -
How to Design Your gRNA for CRISPR Genome Editing
TypeBlog Post...always depend on careful experimental design, execution, and analysis. Many thanks to our guest blogger... -
Viral Vectors 101: Optogenetic Tools
TypeBlog Post... number of strategies have been developed for utilizing light to control GPCR activation and downstream...