We narrowed to 830 results for: eed
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TypeBlog Post... you can show off your work at a conference, you need to first make your poster. While a poster generally... to verbally communicate your work, so you don’t need every little detail on the board. Poster layout...
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Open Resources and Plasmid Tools For Studying C. elegans
TypeBlog Post...The C. elegans community has always emphasized the need for open science and collaboration. The field already...transgene control in Caenorhabditis elegans." Proceedings of the National Academy of Sciences 115.15 (2018... -
Hot Plasmids - October 2020
TypeBlog Post... easier for you to find and use the plasmids you need. If you'd ever like to write about a recent plasmid...of H2B-FT consistently predicted the cell cycle speed across these different cell types. In one example... -
A New Generation of Adenine Base Editors Improves Editing in Primary Human Cells
TypeBlog Post...ABE8 (Gaudelli et al., 2020). The generated ABE8s needed to produce 3 concurrent base edits to withstand...editing single genes is very useful, sometimes, you need to modify multiple genes to generate a cellular ... -
Fluorescent Proteins 101: Introduction to FRET
TypeBlog Post...laboratory may have already created the sensor that you need. FRET biosensors designed to measure specific small...insertion within green fluorescent proteins." Proceedings of the National Academy of Sciences 96.20 (1999... -
Making CRISPR Plasmids Using Fragmid
TypeBlog Post...promoters, N’ and/or C’ terminus, and selection markers. Need fewer components? A spacer can be inserted instead...backbone and genes contain only the Bbsl cut sites needed for the Fragmid cuts, clone in the appropriate ... -
Antibodies 101: Choosing the Right Isotype
TypeBlog Post...dollars on a new secondary antibody if you don’t need it. If, on the other hand, your target is expressed...approach, that is simple - but what about when you need to use an indirect (primary and secondary antibody... -
Hot Plasmids and Viral Preps - March 2021
TypeBlog Post... easier for you to find and use the plasmids you need. Here's what you'll find in this post: Epigenetic... regulators or chromatin-modifying enzymes. The speed and flexibility of the single-pot system will allow... -
Cpf1 Update: Comparison to Cas9 and NgAgo
TypeBlog Post...one RNA rather than the two (tracrRNA and crRNA) needed by Cas9 for cleavage. Now, two new studies show...given that Cpf1 gRNAs are also shorter than those needed for Cas9 (42 nt vs 100 nt.) However, the newly ... -
Experimenting in an Open Source lab: from CRISPR to Cats
TypeBlog Post...locomotion, but our worms are constantly moving so we need good ways to monitor and track them. We have a number...microscopes, including an automated microscope but we need to develop the manual skills at the regular microscope... -
Adenoviral Delivery of CRISPR/Cas9 Aims to Expand Genome Editing to Primary Cells
TypeBlog Post...to knock in corrective genes. For this you would need to provide a DNA template to repair the double strand... homology directed repair and you would probably need to use a two viral vectors system: one vector for... -
Multiplexed Capture of Promoter-enhancer 3D Chromatin Structures Using CRISPR
TypeBlog Post...tag reduces the number of CAPTURE components that need to be delivered to cells from three to two. Lentiviral... remaining CAPTURE 2.0 components eliminates the need to create stable cell lines and allows CAPTURE 2.0... -
No Llamas Required - Synthetic Nanobodies Against Membrane Proteins
TypeBlog Post... reagents in three major steps - all without the need to find a llama farm! To find an optimally binding... Vlieger D, Corbett KS, Torres GM, Wang N, Van Breedam W, Roose K, van Schie L, Hoffmann M, Pöhlmann S... -
Plasmids 101: Protein Expression
TypeBlog Post...protein you are trying to express How much protein you need Your plans for downstream applications In this...than bacterial cells and growing conditions often need to be optimized. Yeast cells are also known for ... -
xCas9: Engineering a CRISPR Variant with PAM Flexibility
TypeBlog Post... xCas9 - here’s what we know so far! Why do we need PAM flexibility? IDT estimates that there is an ...Despite the progress we’ve made, there is still a need for and interest in enzymes with shorter PAM sequences... -
Fluorescent Tagging of Endogenous Genes with SapTrap
TypeBlog Post...arm repair template (Fig. 1, Step 1). There is no need for PCR or cloning, as digestion of the destination...endogenous genes in human cells. To use CRISPaint, users need 3 vectors: 1) a gRNA vector that targets the gene... -
AAV Vector Quality Control: Going the Extra Mile with NGS
TypeBlog Post...CHRM4 gene. When contamination is suspected, we proceed to de novo assembly of the unmapped reads, employing...interrogating the VGS data for small predetermined seed sequences unique to the capsid plasmid. Our recombination... -
Cloning Mammalian Cells with the Agarose Method
TypeBlog Post... cell clones with sterile truncated pipet tips. Indeed, an experienced operator can pick 48 clones from... your colonies are well separated. For this, you need to have some idea of the rate of growth of your ... -
Magnetic Control of Proteins: More than a Dream
TypeBlog Post...mammalian cells, or in purified form, and didn’t need any added cofactors. Figure 2: Fluorescence... and often, including works-in-progress still in need of further study and development like MagLOV. The... -
Plasmids 101: Degron Tags
TypeBlog Post...system — HaloTag and its PROTAC are all that is needed to facilitate degradation. HaloTag is also the ...tag does depend a lot on your unique experimental needs. If your protein’s function is easily perturbed ...