We narrowed to 718 results for: tat
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TypeBlog PostPublishedDec. 8, 2016, 3:30 p.m....actually contain your insert of interest. Simply stated, ccdB makes cloning easier by selecting against...
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Developing Lab Management Software for Biology
TypeBlog PostPublishedAug. 25, 2016, 2:30 p.m.... track the location, quality, growth, and legal status of thousands of plasmids a day, like we do at Addgene... -
Gendered Innovations: Why Does Sex of the Cell Matter?
TypeBlog PostPublishedJuly 21, 2016, 2:30 p.m....Gendered Innovations. This project: 1) develops state-of-the-art methods of sex and gender analysis and... -
Nanoblades: Tiny CRISPR Ninjas for Genome Editing Difficult Cells
TypeBlog PostPublishedSept. 26, 2019, 12:50 p.m.... The team found that "all-in-one" Nanoblades facilitated HDR with either a ssDNA or dsDNA donor template... -
Adenoviral Vector Production and Troubleshooting
TypeBlog PostPublishedJune 14, 2018, 11:44 a.m....ratio for the purified virus should be ~1.3 Quantitative PCR: the number of viral DNA packaged in virions... -
Plasmids 101: Modular Cloning
TypeBlog PostPublishedMarch 12, 2024, 1:15 p.m.... allows users to test a variety of different orientations and components within the system to maximize... -
Simple CRISPR-based Epigenetic Editing: dCas9-directed DNA Demethylation
TypeBlog PostPublishedDec. 14, 2021, 2:15 p.m....without clearly testing whether a certain methylation state causes a condition. To understand mechanisms and... -
CRISPR in the Clinic
TypeBlog PostPublishedNov. 2, 2023, 1:15 p.m....targeted to precisely edit with the goal of ‘fixing’ mutations or introducing a desired edit, but this particular... -
Viral Vectors 101: Calcium Sensors
TypeBlog PostPublishedAug. 10, 2023, 1 p.m....switches from green fluorescence to a red fluorescent state only by simultaneous (1) user-controlled illumination... -
Antibodies 101: Choosing the Right Isotype
TypeBlog PostPublishedApril 6, 2023, 3 p.m....that require high affinity binding, such as immunoprecipitations. Your sample species should also be considered... -
A Look Back at One Year of Plasmid Sharing for COVID-19 Research
TypeBlog PostPublishedJuly 12, 2021, 1:15 p.m....now circulating and plasmids containing these mutations have been deposited at Addgene. Plasmids deposited... -
Hot Plasmids and Viral Preps - March 2021
TypeBlog PostPublishedMarch 23, 2021, 1:15 p.m....vivo studies should always take DNA’s chromatin status into account (Fig 1a). The laboratory of Karmella... -
Plasmids for Endogenous Gene Tagging in Human Cells
TypeBlog PostPublishedApril 6, 2017, 1:02 p.m....it’s also good to make a few single base pair mutations in crRNA target sites found within the homology... -
5 Tips for Troubleshooting Viral Transductions
TypeBlog PostPublishedAug. 11, 2016, 2:23 p.m.... to a target cell by reducing the repulsive electrostatic forces between these two negatively-charged ... -
Cpf1 Update: Comparison to Cas9 and NgAgo
TypeBlog PostPublishedJuly 14, 2016, 2:30 p.m....sophisticated genome-wide analysis. At many of its computationally predicted off-target sites, Cpf1 does not mediate... -
Plasmids 101: Terminators and PolyA signals
TypeBlog PostPublishedMarch 31, 2016, 2:30 p.m....sequence conserved Rho-independent termination annotation for 90 bacterial elements. By Ppgardne at English... -
How-to: 5 Steps to a Great Panel Discussion
TypeBlog PostPublishedOct. 22, 2014, 1:57 p.m....use any slides for the event. Slides are for presentations, not discussions. I will rarely work with a ... -
Tips to Make the Most of a Scientific Conference
TypeBlog PostPublishedMay 23, 2019, 12:26 p.m....themselves and then ask questions. Practice your presentation for both instances. If your poster material ... -
10 Basic tips for mammalian cell culture
TypeBlog PostPublishedJuly 12, 2018, 1:09 p.m....their comfort zone around 37 °C and 5% CO2 and get agitated with sudden changes in temperature (especially... -
Transferable Skills: Negotiation
TypeBlog PostPublishedMarch 3, 2022, 2 p.m....more important to you and why? What are their expectations/needs and how are they different from mine? ...