We narrowed to 749 results for: SOM
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TypeBlog PostPublishedOct. 25, 2018, 1:23 p.m....sounds simple, and it pretty much is, but there are some tips and tricks you can use to obtain optimum transformation... this process right the first time. I’ll lay out some guidelines here. A detailed transformation protocol...
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Simplify Cloning with in vivo Assembly
TypeBlog PostPublishedOct. 18, 2018, 12:37 p.m.... plasmid assembly (if primer design is correct). Some DNA sequences are not easy to amplify by PCR, so...Betaine (1 M) to the PCR mix. When PCR is not possible Some plasmids just won’t amplify! Examples of this are... -
INTEGRATE: Bacterial Genome Engineering Using CRISPR-Transposons
TypeBlog PostPublishedDec. 7, 2020, 2:53 p.m..... Additionally, these transposon also exhibit something called target immunity, whereby multiple proximal... R, Jiang Y, Yang J, Yang S (2020) Multicopy Chromosomal Integration Using CRISPR-Associated Transposases... -
CRISPR 101: RNA Editing with Cas13
TypeBlog PostPublishedJuly 31, 2020, 12:30 p.m....locus, making them more flexible than Cas9/Cpf1. Some Cas13 enzymes prefer targets with a given single...Exchange) system (Abudayyeh et al., 2019). To avoid some of the inherent drawbacks for RNA editing of natural... -
The Effect of COVID-19 on Liu Lab Plasmid Requests From Addgene Data
TypeBlog PostPublishedJuly 16, 2020, 1:15 p.m....would generally not be the same if weekends were somehow imposed on scientists. Figure 6: Model ...regions. Our investigation of model fit revealed some potential instabilities in the China data, so we... -
Negative Can Be Positive: Open AAV Data with Addgene
TypeBlog PostPublishedSept. 6, 2022, 1:15 p.m.... We can all acknowledge that negative data is something every researcher experiences and that it often... J., Bahr-Davidson, J., Smith, P. H., Zhen, Z., Sommer, J. M., Pierce, G. F., & Qu, G. (2005). Identification... -
Great Results Start with Great Standard Curves
TypeBlog PostPublishedAug. 15, 2024, 1:15 p.m....how to create and use a standard curve and provide some general considerations for scientists planning to...of the unknown sample. The unknown should fall somewhere in the middle of the standard curve. If you do... -
Antibodies 101: Producing Recombinant Antibodies
TypeBlog PostPublishedAug. 13, 2024, 1:15 p.m.... to produce your own recombinant antibodies with some molecular biology and cell culture experience. Let...immunocytochemistry. It’s important to note that some antibodies are better suited for certain applications... -
Course-Based Undergraduate Research Experiences (CUREs)
TypeBlog PostPublishedFeb. 9, 2023, 2:15 p.m....many facts but the training of the mind to think something that cannot be learned from textbooks” (Brian,...Biochemistry and Molecular Biology Annual Meeting. Some of my students published their work identifying ... -
Minigenomes - a Safe Way to Study Dangerous Viruses Like the Ebola Virus
TypeBlog PostPublishedMarch 17, 2016, 2:30 p.m...., experiments can be performed in the absence of some viral proteins (compared to viral infection). Therefore...allow for efficient polymerase activity, whereas some ratios result in significantly reduced activity ... -
Tips for Screening with Yeast Two Hybrid Systems
TypeBlog PostPublishedOct. 22, 2015, 2:30 p.m....Researchers also discovered the modular format of some transcriptional activators: that the DNA binding...that use auxotrophic rescue genes as reporters and some that repress instead of activate transcription. ... -
A Career in Grants: How To Become a Grant Professional
TypeBlog PostPublishedAug. 20, 2015, 2:30 p.m.... for an organization in a position that required some involvement in the grants process and managing programs...resources. 3. Get a mentor, find your people Find someone who is working or has worked as a Grant Professional... -
Designing Your Chalk Talk for the Academic Job Interview
TypeBlog PostPublishedMarch 12, 2019, 1:37 p.m....talk is quite simple. It's you, a dry erase board, some markers (chalk is rare these days), and a room of..., if you cannot describe the likely outcome with some specifics, the search committee member cannot either... -
The PAM Requirement and Expanding CRISPR Beyond SpCas9
TypeBlog PostPublishedAug. 20, 2020, 2:30 p.m....compared to wild-type SpCas9, which also displays some cleavage with an NGA PAM. This variant may increase...potentially reversible since there is no genomic edit. Some Cas13 enzymes require a single base protospacer ... -
New CRISPR Tools: Cas7-11 and PASTE
TypeBlog PostPublishedFeb. 17, 2022, 2 p.m....variety of related bacteria with similar Cas systems. Some of these Cas systems have enzymes small enough to...could likely do it using Prime editing alongside some creative (and significant!) protein engineering.... -
Hot Plasmids - November 2023
TypeBlog PostPublishedNov. 14, 2023, 3:35 a.m....generate seven new prime editors, PE6a–g, that overcome some current prime limitations and enable impressive ...protein interactions or map a local proteome, but some applications have been challenging or inaccessible... -
Viral Production at Addgene
TypeBlog PostPublishedOct. 24, 2023, 1:15 p.m....cultures are inspected for sterility. Transducibility Some viral vectors are tested in vitro and in vivo for...gene expression and/or function. These data are sometimes reported or posted on the material page for the... -
Hot Plasmids Spring 2024
TypeBlog PostPublishedMay 23, 2024, 1:15 p.m....Every few months we highlight some of the new plasmids, antibodies, and viral preps in our repository...number of cell types at different genomic loci — in some cases, over 20-fold higher editing than PEmax. The... -
Plasmids 101: Broad Host Range Plasmids
TypeBlog PostPublishedApril 11, 2024, 1:15 p.m....plasmid can transfer to, replicate in, and persist in. Some plasmids have a narrow host range, while others ...fully understood, but scientists have identified some of the features that confer broad host range. These... -
Viral Vectors 101: Preparing Pooled Libraries
TypeBlog PostPublishedJuly 13, 2023, 1:15 p.m....anyone who has worked with individual plasmids knows, some plasmids amplify well and others don’t. The size...s far better to verify via NGS now than to learn some of your plasmids didn’t amplify after your screen...