We narrowed to 565 results for: mme
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TypeBlog Post... it's not always recognized and valued for its immense importance, it may well be what determines whether...
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Antibodies 101: Flow Cytometry Controls
TypeBlog Post... appropriate isotype controls linked on their commercial antibody pages. Flow cytometry can be a complicated... -
Protein Tagging with CRISPR/Cas9: A Conversation with Mendenhall and Myers
TypeBlog Post...percentage of the proteins inside a cell have a commercial antibody against them. There’s also a question... -
Back to Bacteria: CRISPR gRNA Multiplexing Using tRNAs
TypeBlog Post...thoughts about this technology, leave them in the comments below. References Boosting CRISPR/Cas9 multiplex... -
Form Your Own Peer Mentoring Group: A How-To Guide for Scientists
TypeBlog Post... you involved in Peer Mentoring relationships? Comment below with ideas from your own mentoring group ... -
Will You Be My Mentor? Finding and Asking for Mentoring Support
TypeBlog Post...and make sure to choose one that comes highly recommended from someone you trust. A good coach can make... -
Kiran Musunuru on the Newest TALEN Genome-Editing System
TypeBlog Post...the DNA-binding domain is modifiable and can be programmed to bind to essentially any DNA sequence desired... -
Antibodies 101: Secondary Antibodies
TypeBlog Post...blot can be run in a single day, I really cannot recommend it except in the most dire of circumstances.) ... -
What's New in CRISPR - November 2021
TypeBlog Post...Nature Biotechnology Find the Cas12f-GE plasmids Programmed genome editing by a miniature CRISPR-Cas12f nuclease... -
Antibodies 101: Fab Fragments
TypeBlog Post...Imagine an antibody. Do you immediately visualize a Y-shaped protein reminiscent of the Addgene mascot... -
Choosing the B(right)est Fluorescent Protein: Aggregation Tendency
TypeBlog Post...monomer in the cell type tested. To conclude, we recommend that you try a couple of different fluorescent... -
Stabilized Bacterial Promoters: Constant Gene Expression at any Copy Number
TypeBlog Post...protein as the repressor because TALEs can be programmed to bind tightly to arbitrary DNA sequences and... -
Plasmids 101: The protein expression toolbox
TypeBlog Post...References References Nabet et al. The dTAG system for immediate and target-specific protein degradation. Nature... -
CRISPR 101: Cas9 vs. The Other Cas(s)
TypeBlog Post...Lucas, Burstein, David, Chen, S., Janice, et. al. Programmed DNA destruction by miniature CRISPR-Cas14 enzymes... -
It’s Bioelectric! An Exciting Interdisciplinary Field of Research
TypeBlog Post... al., 2011). Additionally, researchers have reprogrammed regenerating tissues without using genome engineering... -
Troubleshooting Your Plasmid Cloning Experiment
TypeBlog Post...major companies selling PCR reagents. Nowadays commercial polymerases are very efficient, but if you are... -
Human Germline Editing Using CRISPR
TypeBlog Post...probably seen this study (and various articles and commentaries) pop up on Twitter and Facebook, shared by biologists... -
Lighting Up Cell Signaling with Photoswitchable Kinases
TypeBlog Post...downstream steps. It’s also possible to determine immediate effects of signaling vs the delayed effects because... -
Addgene's Tips for Plasmid Quality Control
TypeBlog Post...Tell us your favorite sequencing tricks in the comments section below. Additional Resources on the Addgene... -
The Future of Research Symposium Boston 2015
TypeBlog Post...hired to produce results, not scientists” These comments are well correlated with published data. For example...