We narrowed to 949 results for: APP

...chaperone NPM2, but the technique should be widely applicable to other targets. The modular system of linkers...scFvs for other targets or could be used for applications beyond cryo-EM.   Find plasmids for MagIC-Cryo-EM...plunge freezing represents a convenient, effective approach to protecting your cryo-EM samples from damage...optimizing prime editing systems for specific applications! Delivering prime editors (PEs) via engineered...

...Feeling like an apple will fall up instead of down when dropped will not make it happen. In a time when...earlier analogy, no amount of shouting will make an apple fall up. As scientist and politician Rush Holt said... Rush Holt: Lawmakers need to use a scientific approach to formulating views Pew Research Center: Public...

...Madison, Wisconsin. It is commonly cited that approximately one-third of cellular proteins are modified ...phosphorylation is far more prevalent than previously appreciated. PhosphoSitePlus, one of the most inclusive databases...protein modification within the context of its appropriate regulation. To avoid these problems, it is also...requires a molecular toolkit containing the OTS, an appropriate bacterial host strain for protein production,...

...of interest (see below for recommend amounts) Appropriate restriction enzyme (see manufacturer's instructions...instructions for proper ammount) Approrpriate restriction digest buffer (see manufacturer's instructions) ...as Addgene's Sequence Analyzer . Determine an appropriate reaction buffer by reading the instructions for...The amount of DNA that you cut depends on your application. A diagnostic digest typically involves ∼500 ...volume usually varies from 10-50 µL depending on application and is largely determined by the volume of DNA...better. Mix gently by pipetting. Incubate tube at appropriate temperature (usually 37 °C) for 1 hour. Always...manufacturer’s instructions. Pro-Tip Depending on the application and the amount of DNA in the reaction, incubation...

...PBS, remove the wash, and dispose of it in an appropriate waste container. Fix each well with 500 µL of...as methanol or acetone may be better for some applications. Remove the paraformaldehyde and follow your...safety guidelines for disposing of waste in the appropriate container. Wash 3x for 5 min in 500 µL PBS on...permeabilization buffer and dispose of it in an appropriate waste container. Wash 3x for 5 min in 500 µL ... the blocking buffer and dispose of it in an appropriate waste container. Dilute the primary antibody ...the primary antibody and dispose of it in an appropriate waste container. Wash 3x for 5 min in 500 µL ...min at RT in the dark. Pro-Tip The plate can be wrapped in foil to block light. Remove the secondary antibody...

...interact, the labs of Baljit Khakh and colleagues mapped their cell-surface proteomes (Wu et al., 2025)....an inverted topology of FRCaMP (itself based on mApple, which means it likely has the blue-light photoswitching...their sensors in a variety of neuronal imaging applications, including confocal and widefield imaging, two-photon...transcription-translation system (Figure 6). This approach eliminates the need for expensive reagents and...

...toward the cathode (- charge). When the voltage is applied across the gel, the DNA migrates toward the anode...want a “recipient plasmid : insert ratio” of approximately 1:3. Since the number of base pairs for each...should also verify that you are plating on the appropriate antibiotic and try varying the “recipient plasmid...Ideally, once you know that your plasmid has an appropriately sized insert, you should send it for sanger ...

...transposition activity  Tol2 transposon plasmids    Applications of transposons Now that you’ve learned about...and Tol2), each of which has several different applications (mutagenesis screens, transgenic animals, gene...Garcia-Perez J (2010) DNA Transposons: Nature and Applications in Genomics. CG 11:115–128. https://doi.org/...Tools: A Review and Guide through Mechanisms and Applications of Sleeping Beauty, piggyBac and Tol2 for Genome...

...cells with no Cas9 should appear green and cells with functional Cas9 should appear less green. Note that ...the population, so some of the cells will still appear green despite having active Cas9 (see tip 2). Pro-Tips...by the presence of DNA cleavage products. The appearance of the 428 bp band indicates edits in the BRAF...

...Shakespeare for the first time. The discovery and application of CRISPR-Cas9 kicked off over a decade of frenzied...classification system will help you gain a deeper appreciation and understanding of CRISPR, and perhaps provide...mechanisms in type I-C CRISPR-Cas3 for genome-editing applications. Molecular Cell, 84(3), 463-475.e5. https://...Mashimo, T. (2022b). Genome editing technology and applications with the type I CRISPR system. Gene and Genome...

...protein composition. It is used for a variety of applications such as measuring target protein expression ...stain the intracellular target. When using this approach, avoid fixation-sensitive fluorochromes such as...assaying a secreted protein, first block the Golgi apparatus with Brefeldin A to inhibit secretion and then...antibodies during the flow cytometry experiment and will appear as a distinct population. After initially gating...

...up. Applications of photoactivatable fluorescent proteins Some of the most important applications for ...level of background fluorescence. For any PA-FP application, the brighter the fluorescence the better. More...photostable green and red states. Beyond these imaging applications PA-FPs have been developed for use in yeast,...

...Callaway   For researchers in countries with applicable export control exceptions for rabies and VSV-...VSV-G genes, plasmids ship out approximately three weeks faster, as no license, or license fee, will be ...please feel free to email [email protected]. We’ll be happy to help! A quick note: While this blog post is accurate...

...PAM is so flexible in this state that it doesn’t appear in the crystal structure (Figure 2) at all. When...cleavage. Nucleotides 11-20 are disordered and don’t appear in the Figure 3 crystal structure, reflecting the...which stabilizes the last base pair with an end-capping loop (Nishimasu et al., 2014). This cap is where...with and better understand how to manipulate it. Happy CRISPRing!   Molecular graphics and analyses performed...

...concentration disolved in the appropriate liquid solvent. See table to the right for appropriate antibiotic concentrations...Strains Grow Assuming the appropriate strains were streaked on the appropriate plates, then if both strains... LB-agar powder you’ve measured out into an appropriately sized bottle for autoclaving. We make 400 mL...autoclave. Be sure to check the literature for an appropriate sterilization technique if you are working with... wipe down with a paper towel. Count out the appropriate number of plates and stack them on your lab bench...of molten gel mix, a tube rack containing the appropriate antibiotics, and a section for active pouring...antibiotic. Incubate both plates overnight at the appropriate growth temperature and check for growth. See ...

...show the interactions between amino acids in an approximate, two-dimensional map. The Baker Lab wanted to...novel, the principles that created it have been applied to numerous other protein design goals, both from...drugs, all developed with their protein design approach. Congratulations to David Baker, Demis Hassabis...

...This edition of the contest is our traditional approach. You might decorate your lab in pipette tip snowflakes...piece of advice - get your PI or lab manager’s approval before letting your imagination run loose on the...diorama. Or maybe you want to create a stack of wrapped gifts using life science catalog pages. Make your...

...target and use FRET flurophores for a variety of applications. While editing this post, I learned a lot about...this post to anyone wondering if and how they can apply FRET in their own research. All posts from July ...Blogger Form and we'll be in contact with you ASAP. Happy Reading! Tyler ...

...concluded, Addgene and Seeding Labs will be opening applications for a second round of plasmid awards on June...excited to discover what new and creative ideas applicants will propose for plasmids from the Addgene community...regions in the near future. Additional Resources Apply to Recieve Equipment through Seeding Labs' Instrumental...

...brains on how they've managed to keep themselves happy during their time in grad school. As you'll learn...student communities 5:59 - 8:16 : What has made you unhappy in grad school? As part of this discussion, we ...to the right that illustrate a grad student's happiness v time throughout graduate school. This is, of...