We narrowed to 881 results for: NSI
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TypeBlog Post...2008), but there are still many more features to consider when designing a full gene. A non-exhaustive list...
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Using Video to Share Your Science: We Share Science
TypeBlog Post...Evolution of Scientific Impact Data Freedom: The Expansion of Data Sharing in Research Publications Resources... -
Rett Syndrome: A History of Research and Therapeutic Outlooks
TypeBlog Post...fine-tuning dosage so that enough wild-type MECP2 is made inside the cells, but this is exciting progress in tackling... -
To Codon Optimize or Not: That is the Question
TypeBlog Post...Molecular Biology Reference Read about genetic code expansion Browse our plasmid collection page ... -
Overcoming the AAV Size Limitation for CRISPR Delivery
TypeBlog Post...streptavidin and next-generation sequencing). Using this sensitive method, they found that SaCas9 did not display... -
The PAM Requirement and Expanding CRISPR Beyond SpCas9
TypeBlog Post...Wolfe SA, Sontheimer EJ (2018) NmeCas9 is an intrinsically high-fidelity genome-editing platform. Genome... -
Plasmids 101: Broad Host Range Plasmids
TypeBlog Post...host range recombinant vectors Replicons, which consist of a plasmid’s ori and all of its control elements... -
Harnessing TnpB for Genome Editing: A Compact and Versatile Tool for Your Research
TypeBlog Post...plant and animal systems. Importantly, they allow transient delivery, enabling transgene-free genome editing... -
Transferable Skills Guide: Time Management
TypeBlog Post.... For instance, even if I had planned my day extensively, my lack of desire to go sit in the tissue culture... -
Harnessing Bacterial Toxins for Allelic Exchange
TypeBlog Post...unmarked mutants, but it frequently requires considerable optimization to ensure strong counter-selection... -
3 Tips to Improve HDR Efficiency for CRISPR Editing in Human Cells
TypeBlog Post... and model systems. We have used CRISPR/Cas9 extensively for the purpose of making sequence-specific changes... -
Thoughts on the Future of Research 2015 Boston Symposium
TypeBlog Post...different universities are trying to compile more comprehensive demographic information about the postdoc work... -
Easi-CRISPR: Generating Knock-In and Conditional Mouse Models
TypeBlog Post...Commons 4.0 license. The research groups responsible for Easi-CRISPR have also recently developed ... -
CRISPR 101: Epigenetics and Editing the Epigenome
TypeBlog Post...cells. For example, KRAB induced silencing was transient and quickly reversed in culture. However, DNMT3A-induced... -
Technique: Probe Phage Genomes for Host Binding Proteins
TypeBlog Post...transformants for appropriately sized inserts. We consider a library worth using if at least 40% of colonies... -
Plasmids 101: Restriction Cloning
TypeBlog Post...stains): Stain Pre or Post Run? Visualization Sensitivity (ng DNA) SYBR Safe Pre and Post Blue or UV ... -
Building Global Connections with the International Mentorship Program USA-EUROPE
TypeBlog Post...possible a significant qualitative and quantitative expansion in the 2015-2016 academic year. This year, the... -
A History of Genome Engineering in Popular Culture
TypeBlog Post... scientific community and remind us to always consider the ethics and broader implications of our research... -
DNA Quantification
TypeProtocol...such as TE). You will get much more accurate and consistent readings from DNA in a buffered solution. Reference... -
Protocol - How to Design Primers
TypeProtocol...for broader pairing capabilities. Taking into consideration the information above, primers should generally... -
CRISPR 101: Multiplex Expression of gRNAs
TypeBlog Post...be expressed simultaneously. Vectors for both transient expression and Agrobacterium-mediated transformation... -
Protocol - How to Perform Sequence Analysis
TypeProtocol... experiments. There are a number of factors to consider when selecting sequencing primers, including: ... -
Protocol - How to Perform a Diagnostic Digest
TypeProtocol... to test individual clones before use of more expensive forms of plasmid verification, such as DNA sequencing... -
Protocols for Molecular Biology, Plasmid Cloning, and Viral Preps
TypeProtocol...Watch the Video! How to Design a Primer Key considerations when designing primers Watch the Video! Sequence... -
Lab Safety for Biosafety Levels One and Two
TypeProtocol...anyone else associated with Addgene, can be held responsible for your use of the information contained in ... -
Protocol - Bacterial Transformation
TypeProtocol...The lowest efficiency cells (usually the least expensive) are fine for transforming plasmid DNA for the... -
Lentivirus Production
TypeProtocol...batch of 1 mg/mL PEI and for each cell line. Considerations Before You Start The health of the packaging... -
Protocol - How to Run an Agarose Gel
TypeProtocol...high percentage of glycerol that increases the density of your DNA sample causing it settle to the bottom... -
Plasmid Cloning by PCR (with Protocols)
TypeProtocol...Cloning The basic PCR primers for molecular cloning consist of: Leader Sequence: Extra base pairs on the 5'... -
Antibody Validation Using the Indirect ELISA Method
TypeProtocol...support reproducibility in science. General Considerations The ELISA can be completed in a single day ... -
Protocol - pLKO.1 – TRC Cloning Vector
TypeProtocol...suitable for handling HIV-derivative viruses. For transient knockdown of protein expression, you may transfect...