We narrowed to 1,019 results for: CAL;
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TypeBlog Post...Find plasmids from this publication at Addgene. Scalable and versatile genome editing using linear DNAs...Caenorhabditis elegans. Paix A, Wang Y, Smith HE, Lee CY, Calidas D, Lu T, Smith J, Schmidt H, Krause MW, Seydoux...
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Another Pathway into Cells: iTOP
TypeBlog Post...type; however, their usage has been limited by technical problems. For instance, it’s much more difficult...presence of the CPP may alter protein function or localization. Thus, the usefulness of CPPs must be evaluated... -
Mentoring for Scientists: I Have a Mentor, What Now?
TypeBlog Post... Listen to our podcast interview with Harvard Medical School researcher Connie Cepko to learn about her...mentoring meetings a priority. Schedule meetings or calls regularly and don’t cancel, so that you drive progress... -
Extracurricular Activities for a Strong Science Career Path
TypeBlog Post...developed a web-based, career-planning platform called the Individual Development Plan (IDP) and uses ... Outreach activities (e.g. Volunteer at a local high school science class: Science Club for Girls... -
How Dry Ice Affects Viral Vector Sample pH & How to Avoid It
TypeBlog Post...aqueous samples might be affected by dry ice, and specifically how dry ice can affect virus from Addgene. ...never stored on dry ice/exposed to CO2 (Fig. 5). Basically, the CO2 goes in and the CO2 goes out. Conclusions... -
Components of CRISPR/Cas9
TypeBlog Post... to modify the desired genomic locus. Some historical notes CRISPR arrays in bacterial genomes consist...arrays, they did not know their functions and simply called the repeated elements “direct repeats” and the ... -
Fluorescent CRISPR Reporters: SRIRACCHA and GEmCherry2
TypeBlog Post...end joining (NHEJ). In these reporters, editing typically results in a change in the fluorescent readout...stimulated homology-directed repair. Journal of Biological Chemistry 292:6148–6162 . https://doi.org/10.1074... -
Expanding the Targeting Scope and Editing Efficiency of Adenine Base Editors
TypeBlog Post... specific DNA base changes and consist of a catalytically impaired Cas protein (dCas or Cas nickase) fused...previously uneditable sequences. Four DNA base swaps, so called point mutations that change C to T, G to A, A to... -
Improved Plasmid Maps Powered by SnapGene
TypeBlog Post...powered plasmid maps far easier to navigate. These practical and effective changes will give you the ability... and “Sequence” tabs. BLAST Use the Basic Local Alignment Search Tool (BLAST) via the NCBI website... -
Hot Plasmids - February 2022
TypeBlog Post...anti-FLAG-FB-GFP binding to FLAG-tag H2B for nuclear localization. (c) Applications of anti-FLAG-FB-GFP labeling...4xFLAG-mCherry-β-actin), and mitochondrial (mito-mCherry-1xFLAG) localization. Adapted from Liu et al. 2021. Anti-FLAG... -
Flow Cytometry Readouts: Yes, No, and Everything in Between
TypeBlog Post... a downregulation of signal, though it’s hard to call from this plot. The red (bottom) peak overlaps with...Research Assistant in Arlene Sharpe’s lab at Harvard Medical School. More resources on the Addgene blog Antibodies... -
Viral Vectors 101: Gamma-Retroviral Packaging Systems
TypeBlog Post...transfer plasmid sequences into the host genome. Typically, it is the sequences between and including the...pseudotyping. Figure 1: Genome of a prototypical gamma-retrovirus. Frequently asked questions... -
Antibodies 101: Flow Cytometry Controls
TypeBlog Post...sample. The isotype antibody will be virtually identical to the antibody for your marker of interest. It...research technician in Arlene Sharpe's lab at Harvard Medical School. More resources on the Addgene blog Introduction... -
How to Keep a Lab Notebook for Bioinformatic Analyses
TypeBlog Post... the following, which are later printed for my physical lab notebook, along with any figures generated...between each word can make it difficult to accurately call a file. Version control your commonly used scripts... -
CRISPR Library Amplification
TypeProtocol...the Qiagen HiSpeed Maxi Kit (one conical is its own Maxiprep). Critical Do not freeze pellets for later...libraries up to 200,000 individual plasmids and can be scaled according to the actual number. Required Quality...selection). This recombination, at a low rate, is not typically a problem as these sequences are not efficiently...200,000 individual plasmids. For larger libraries scale the number of cells and DNA accordingly. Pro-Tip...cells) Less library DNA can be used but this dramatically increases the chances of individual plasmids...Cell Spreaders (VWR, 60828-680) 5 mL and 10 mL Serological pipettes Ice slurry (Ice bucket with ice and ...normal growth is expected to work. 50 mL Falcon Conical tubes (Fisher, 14-432-22) Reagent Preparation Prepare... -
Transferable Skills Guide: Cross-team Communication
TypeBlog Post...out the sources of miscommunication and b) find practical solutions. My PhD prepared me remarkably well...answer to these questions--which were real, not hypothetical--was clearly “no.” When there was room for misinterpretation... -
Summer SciComm Series: Cognitive Load
TypeBlog Post...intuitive, or logical to a biologist that are not at all obvious, intuitive, or logical to a layperson... -
CRISPR 101: Cas9 vs. The Other Cas(s)
TypeBlog Post...once it is engaged by its target, it will non-specifically cut ssDNA. This feature is shared by other Cas... potential as a viral therapeutic that could specifically degrade target viral RNA. For more information... -
New Tool for Lineage Tracing: The ClonTracer Library
TypeBlog Post...library, propagated it, separated it into roughly identical replicate groups, and treated these groups with...would have different labels - i.e. they would stochastically arise from different cells throughout the treatment... -
Plasmids 101: Golden Gate Cloning
TypeBlog Post...Another strength of Golden Gate cloning is its scalability. Unique 4 base overhangs can be used to assemble...design of flanking overhangs. Although there are theoretically 256 distinct flanking sequences, sequences that...