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We narrowed to 931 results for: TIM

Showing: 181 - 210 of 931 results
  1. Celebrating Accomplishments in the Lab

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    Blog Post
    ...growth along the way. Take time to celebrate the lab’s achievements and enjoy time with friends and family...accomplishments? Any tips on making time to relax and/or enjoy time away from the bench? We would love ...their team's hard work? Do succesful scientists have time for fun and life outside of the lab? This final ...”. He also cooks and cleans with his family, “sometimes listening to audiobooks.” Church and his family...family. And as the school year winds down, take some time to have fun outside the lab! How does your lab celebrate...George Church (Harvard Medical School) for taking the time to speak with us throughout this series about how...
  2. Career Insights: Technical Support Specialist

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    Blog Post
    ...companies), and as far as I remember, it was the first time that I was absolutely convinced it was the company...specialist for 4 years. Read on for insights from my time in technical support including tips, advantages,...required for a role in technical support? It takes some time (several years) to build up comprehensive lab experience...companies have dedicated technical support teams, sometimes comprised of several layers of support: A front-line...incoming requests and answers questions that are less time consuming and/or less technically challenging. Alongside...listen to the many individual stories and get (sometimes refreshing) insights into how other scientists...shortage of amusing reports where someone tries to “optimize” a particular standard lab protocol. For example...
  3. How to Write a Scientific Review Article

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    Blog Post
    ...retreat to the woods for months at a time, so take advantage of whatever time you have. If you’re like me, you... I use the software to add the citations in real time as I write. Things are going to get a little crazy...it’s practical because there simply isn’t enough time to read every single paper. I also learned to appreciate...Like I mentioned, I also added citations in real time as I wrote, so each statement was referenced even...: initially I felt that I needed a huge chunk of time to sit down and get anything done, so unless I had... I realized how elusive a free two hour block of time was. Eventually, I learned that I was most productive... dozens of drafts of the manuscript. This is the time to transform the document into something cohesive...
  4. Mesothelioma - Causes, Symptoms, and Treatment

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    Blog Post
    ...The average latency period (time from first asbestos exposure to the time of diagnosis) is about 35 years... small, hook-like shape of asbestos fibers. Over time these embedded asbestos fibers cause inflammation...which can cause mesothelial cells to mutate and ultimately form cancerous tumors.  This process is not quick...decades from the first exposure to asbestos to the time when someone starts seeing – or feeling – the first...years, but it usually ranges from 20-50 years and sometimes longer. There is no known safe level of exposure...mesothelioma is often misdiagnosed, meaning that by the time it has caught it has usually started to spread (...asbestos for years, or they are exposed even one time. Doctors and researchers don’t entirely understand...
  5. CRISPR-based Genome Editing Systems For Editing in E. coli

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    Blog Post
    ...Sciences. In the Yang lab, we’re continually optimizing the use of CRISPR editing systems in bacteria...strains, but also in E. coli B and W strains. The optimized plasmid curing method was much simpler and took...Tatumella citrea, with a total of 70 sites edited. We optimized the strategy for plasmid curing, providing users...ways: In our initial paper, we used MUCICAT to optimize the gene dosage of glucose dehydrogenase and generated...achieve glucose dehydrogenase expression that is 2.6 times higher when compared to the industrial strain. In...obtained a stable and high-yielding strain which had 6 times the yield of the industrial strain. Not only is ...with different gene dosages to facilitate swift optimization of strains. Multiple induction systems to choose...
  6. Avoiding the Dark Side of Fluorescent Protein Fusions with mOX FPs

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    Blog Post
    ...Erik L. Snapp and Lindsey M. Costantini. "You underestimate the power of the Dark Side." --Darth Vader in... Fusions Observing a bright signal for the first time after cloning an FP fusion with your favorite protein...fluorescent protein fusions in live cells in real time. Previously, we have described a number of practical...protein function and this could lead to under and overestimation of fusion protein activity. We encourage investigators...starting by using the newly published oxidative optimized palette of FPs (moxFPs) [5]. The moxFPs overcome...characteristics of the moxFPs are comparable to the non-optimized parental proteins. Our recent publication illustrated...fluorescent signal achieved when utilizing an optimized moxFP as opposed to standard FPs. The increase...
  7. Plasmids 101: Control Plasmids

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    Blog Post
    ... and optimization of the transfection reagents and process. It is important to note that optimal experimental...experiments, the biological controls are more time consuming and ultimately more important. Ideally, each biological...identify opportunities for troubleshooting or optimization within your experiment. Read on to learn more...the independent variable should be consistent over time and from different preparations of the purified ...and were incubated on the same plate at the same time. Although the replicate control is important, it... whole experiment from start to finish multiple times and on different days. Using our example above, ...controls, performing multiple replicates, and ultimately getting interpretable results: Figure 4: Expression...
  8. Tips for Using FRET in Your Experiments

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    Blog Post
    ...The first time I heard about FRET during a journal club, my guitarist brain automatically thought about... pAquaN1 Cyan Mammalian Expresses mammalian optimized Aquamarine mCerulean N1 Cyan Mammalian Express...pCEP4CyPet-MAMM Cyan Mammalian Expresses mammalian optimized CyPet pCyPet-His Cyan Bacterial Expresses CyPet...pCEP4YPet-MAMM Yellow Mammalian Expresses mammalian optimized YPet pYPet-His Yellow Bacterial Expresses YPet...acceptor photobleaching method and the fluorescence lifetime imaging microscopy (FLIM) method. Acceptor photobleaching...not to destroy the donor molecule. Fluorescence lifetime imaging microscopy method FLIM has been developed...measuring FRET. FLIM measures the fluorescence decay time of the donor. When FRET occurs between the pairs...
  9. 28 Hot Plasmid Technologies from 2015

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    Blog Post
    ...heterodimer in response to blue light, which will ultimately co-localize the VP64 transactivator with a dCas9... innovative ways. The principle of protein multimerization is seen in many important biological contexts...copies of a protein to a target polypeptide. Multimerization in the SunTag system occurs via antibody-peptide...single-molecule reporter of intracellular processes. Multimerization via the SunTag system also shows strong upregulation...specified cellular processes or be observed at a later time via DNA sequencing or other readout. Cellular memory...large changes in binding affinity with light stimulation. Indeed oLID showed only a two-fold change in...50 fold change in binding affinity with light stimulation2. The Kuhlman lab created two improved Light ...
  10. CRISPR 101: Cytosine Transversion Editors

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    Blog Post
    ...complementary C. Optimized base editing with eOPTI-CGBE and cOPTI-CGBE Many optimizations had already been...Surprisingly, the team noticed that this editor sometimes introduced C → G edits at certain positions within...were making similar observations around the same time. (The papers were actually published in the same.... Created with BioRender.com. Beyond UNG: Optimizing C → G editors Now that several labs had shown...multi-step cellular repair pathway that is known for sometimes causing double-strand breaks (DSBs). The Fei-Long...common intermediate of CGBE activity, and they are sometimes processed by error-prone non-homologous end joining...editing, we can expect several generations of optimization before the field begins to converge on a set...
  11. An Addgene Co-op: The Intersection of Fun, Friendship, and Work

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    Blog Post
    ...where to start. Thankfully, my managers set aside time for me to complete an online social media certification... meetings didn’t seem much more than numbers. As time passed, and I participated in the discussions, I...first official professional presentation.  My first time in the lab! I got to assist production on a protocol...slide design, discussion items, big takeaways, and timing. The sense of trust and comfort I had with my teammates...only a Slack message away.  When it finally came time for me to present, I thought I would be extremely...days I was up to my neck in to-dos, I also found time to go out to sushi restaurants for lunch with coworkers...the dog.  Cuddles at Olive’s office hours! As my time here comes to an end, my worries about making connections...
  12. Hot Plasmids: Summer 2024

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    Blog Post
    ...cryo-EM grid freezing Engineered and evolved optimizations for prime editing CHARM: A compact epigenetic...requiring a lower concentration of sample — nearly ten times less protein. While the addition of LEAs may bias...2024.02.06.579238.    Engineered and evolved optimizations for prime editing By Emily P. Bentley The David...Liu Lab has made two recent deposits focused on optimizing prime editing systems for specific applications...bp, PASSIGE can integrate cargoes over a hundred times that size (demonstrated up to 10.5 kb) by relying...evolves and engineers Bxb1 recombinase variants to optimize PASSIGE efficiency (Pandey et al., 2024). The ...four-fold improvement over the wild-type enzyme. Find optimized PASSIGE plasmids here!     Figure 3: Schematic...
  13. Five Popular Model Organisms

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    Blog Post
    ...they have a relatively short generation time for mammals - the time between being born and giving birth -...maintained in the lab, and have short generation times that make it easy to study the effects of genetic...simultaneously observe several generations of mice at a time. Because mice are more genetically and physiologically...potential for therapeutic drug discovery as it is estimated that 75% of disease causing genes in humans have...other model systems but can be quite difficult and time consuming. GAL4/UAS was first described in 1993 ... a set of modular vectors that can be used to optimally control gene expression in specific cells of the...groups, easily bred, and produce 50-300 eggs at a time. Zebrafish embryos are also laid and fertilized ...
  14. 3 Tips to Improve HDR Efficiency for CRISPR Editing in Human Cells

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    Blog Post
    ...editing accuracy by preventing re-editing and (2) optimizing “cut-to-mutation distance”. Furthermore (3), ... strategy that was discussed in the field at the time but had never been systematically analyzed: introducing...find the right one Step 2 – Edit the cells a second time using a repair template that corrects the blocking...CRISPR Resources on Addgene's CRISPR Guide Page 2. Optimizing "cut-to-mutation distance"  Even though we had...mutation distance and editing efficiency.   3. Optimizing "cut-to-mutation distance" for homo or heterozygous...that for generating a homozygous HDR event with optimal efficiency a guide RNA targeting a cut <10 bp from... other on each target site.   Figure 3: Optimal cut site to mutation distances for heterozygous...
  15. Safe Port in a Storm...How Addgene is Weathering the Pandemic

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    Blog Post
    ...These are stormy times. It feels like we’re being buffeted by wind and waves and sometimes wonder if we can...Thanks to everyone for being awesome during a tough time. We're all going to get through this and have one....” And we sent the Addgenies home.  At the same time, as Addgene started dealing with this new reality...available to industry requestors as well. This is a time when we need as much open science sharing as we ...’re all doing amazing work during this difficult time. One function that rose to the challenge was our...with labs worldwide closing for unknown amounts of time, we were facing a financial crisis. As a nonprofit...keep new projects on track to succeed at the same time. I began approaching science funding organizations...
  16. Multifunctional Neural Fibers: Modulation from Gut to Brain

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    Blog Post
    ...interest, and stimulate or manipulate responses through neurological means like electric stimulation, drug administration...response to both of these stimulations. The best part? The chemical stimulation was sucrose…..sounds like... The fibers they ended up generating were 10-15 times more flexible than the brain fibers and importantly...microcontroller, NeuroStack coordinates optical stimulation of its associated fibers across multiple channels...authors first tested that the system could induce stimulation in target tissues of a live animal. They started... to the brain tissue. They performed optical stimulation using NeuroStack and the fibers as previously...
  17. Natural or synthetic? How Addgene’s dataset reveals trends in biological innovation

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    Blog Post
    ...of the time in a test set of 173 known synthetic and natural genes.  In designing and optimizing their...how Aditya Kunjapur, a MIT graduate student at the time, got involved. Along with Philipp Pfingstag, a visiting...visiting graduate student from TU München at the time, the team built an algorithm that predicts whether...codon usage biases. But if a gene’s sequence was “optimized” so that it more closely resembles that of the...genes where there are instances of rare codons, sometimes intentionally modulating expression in ways we...-of-origin of engineered DNA This isn’t the only time researchers have used Addgene as a large data set... gene are essential and complementary tools in a time where biological engineering and synthetic biology...
  18. Quantifying DNA? Here are Five DNA Quantification Methods to Consider

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    Blog Post
    ...choose could be based on your downstream application, time, and instrument availability. UV absorbance Using...ug/ml pure dsDNA. Use the following formula to estimate your DNA: Concentration (ug/ml) = A260 reading...quantify your DNA prep. Though this method takes more time to set up in the lab, you might not have to do the...electrophoresis, you only need 1-2 ul of sample and the run time is just a few minutes per sample. During the run...larger fragments. These fragments are quantified over time using a fluorescent dye that intercalates into the...electrophoresis which shows fluorescence units over time. Smaller fragments migrate more quickly than larger...that can be quantified at 595 nm. This method is time consuming and has low sensitivity so it’s not used...
  19. Technique: Probe Phage Genomes for Host Binding Proteins

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    Blog Post
    ...that get smaller in size as a function of digestion time. For phage DNA that is refractory to enzymatic digestion...be selected for by manipulating the nebulization time and pressure. Nebulization units, which can be purchased...fragments falling between 1 and 3 kb results in optimal likelihood of capturing a whole RBP gene without...80°C) followed by 5 min at 37°C (each repeated 5 times) works well. Leaving the membrane overnight in the...to enhance folding of the recombinant proteins. Optimal salt concentration will vary with each protein,...at room temperature as opposed to overnight at optimal growth temperature. If you’re lucky enough to have...the membrane to probing with cells in order to optimize this portion of the assay before attempting it...
  20. Hot Plasmids - October 2020

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    Blog Post
    ... in live cells. The fluorescent timer emits blue light around the time of synthesis and, after a few hours...Fluorescent protein system for C. elegans Fluorescent timers for studying cell cycle length The CRISPR corner...pattern of hippocampal adult-born granule cells over time that were not previously possible.   Bensussen ...-wrmScarlet is a new split red FP that is three times brighter in worms than split-sfCherry3. It was created...cell cycle length with a histone-fused fluorescent timer By Kate Harten DeMaio Studies of the cell cycle ...Yale University fused a color-changing fluorescent timer (FT) protein to the histone H2B that allows for  ... Get the plasmids at Addgene Sc++ is a codon-optimized, engineered Streptococcus canis Cas9 nuclease ...
  21. Tips for Titering Your Lentiviral Preps

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    Blog Post
    ...transfected and harvested your lentivirus. Now it’s time to move ahead with your infection and make your ... of virus you actually have in your prep. Taking time to properly titer your virus will not only ensure... the best possible way, but it may also save you time in the long run. Read on for an overview of the ... based off of p24 quantification tend to be overestimates since they can include free p24 and defective...assay, titering via measurement of viral RNA can overestimate the amount of infectious virus in a prep as ...physical titer, there is a risk that they may underestimate viral titer as these assays cannot distinguish...integration events, reducing the possibility of underestimating the viral titer. The main drawback of this ...
  22. Academic vs. Industry Postdocs

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    Blog Post
    ...industry postdocs have a set time limit. At AstraZeneca, this is three years. This time limit can feel like a...might have less time to explore scientifically since you can’t afford to spend too much time working on something...Pros and cons: The academic vs. industry postdoc  Time: Academic postdocs can be long—5 years or more, ... Also, if you work in industry for any length of time, you’ll know more people in industry, which means...numbers of publications, which may take a longer time to acquire. Learning about drug discovery: Unless...as AstraZeneca, will hire their postdocs for full-time positions should a position open up. Other companies...
  23. Polymerase Chain Reaction Overview and Applications

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    Blog Post
    ...small amount of DNA can be copied many many times in a short time period. PCR was invented in the early 1980s...denaturation, annealing and extension is repeated 25-35 times to exponentially replicate the target DNA of interest...which would slow or stop PCR amplification. Other times, the PCR reaction may not be 100% efficient and ...polymerase chain reaction (qPCR) also known as real time PCR is a PCR technique used for measuring a starting...require a reference or standard curve, which can be time consuming and challenging to get right. ddPCR uses...an extremely useful PCR method that can help save time and effort in the laboratory.  There are two main... different pathogens in one specimen saving both time and effort. Scientists can also utilize multiplex...
  24. Which Fluorescent Protein Should I Use?

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    Blog Post
    ... anaerobic conditions. Maturation Time: Maturation time is the time it takes the FP to correctly fold ...Dreiklang). Fluorescent Timers (FT): These proteins change their color over time. Therefore, these can ...can be used as “timers” for cellular processes following their activation. The four main FTs are called ...and DsRed ~10hours. Temperature: FPs maturation times and fluorescent intensity can be affected by the...temperature. For instance, enhanced GFP (EGFP) was optimized for 37°C, and is therefore most suited for mammalian...
  25. Tips for arabidopsis transformation

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    Blog Post
    ...are some tips and tricks you can use to obtain optimum transformation efficiency. It can take 6-8 weeks...pretty important to get this process right the first time. I’ll lay out some guidelines here. A detailed transformation...transform early, your plants will still have plenty of time to produce seeds after you expose the flowers to...you are transforming more than one construct at a time. For detailed protocols, volumes, spin speeds, ...agrobacterium: Getting a transformant takes a long time. Make sure the agrobacterial culture you are growing...cells in your culture will no longer be viable. The time this will take depends on the volume of culture ...inoculated from a colony on a plate will reach an optimal density in 18-24 hours. I then add 0.5 mL of this...
  26. Tips and Tricks for Using Golden Gate Modular Cloning (MoClo)

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    Blog Post
    ...This post was written by Alfonso Timoneda, with significant contributions from Robert Hurt and Mohamed...ligation steps together in the same tube at the same time, however, it can prove itself to be quite the mental...and arguably the most important, is to take some time to sit down, plan your cloning, and have a clear...yourself using PCR, but gene synthesis can save you time. Using gene synthesis, you can request the sites...plasmids from your original Addgene kit plate as few times as possible and always under sterile conditions....insert to vector’ can be defined by you.   Save time, go high throughput You are ready to perform your... but you have a high number to get through. It’s time to think big and perform your assemblies in a high-throughput...
  27. Hot Plasmids: Fall 2024

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    Blog Post
    ... for structural studies of E3 ligase cereblon Optimized mScarlet-based tags for live imaging in C. elegans.../10.1038/s41467-024-52871-9. PMID 39406745. Optimizing mScarlet tags for live imaging in C. elegans ...for mScarlet3 and mScarlet-I3 that were codon-optimized for C. elegans and included artificial introns...mScarlet3 was 50% brighter than the original worm-optimized wrmScarlet. mScarlet-I3, while initially dimmer... et al., 2024 under CC-BY license.  These optimized fluorescent proteins will be a useful addition...efficiencies of up to about 9% of colonies (102 to 104 times higher than traditional homologous recombination...mechanical forces with PILATeS By Emily P. Bentley Time to get flexible! Alex Dunn’s lab and collaborators...
  28. Advanced Uses of Cre-lox and Flp-FRT - A Neuroscientist’s View

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    Blog Post
    ...loxP sites (For details see Cre-lox blog post). Optimizing FLP FRT through smart engineering Different FLP...first version of FLP discovered has a temperature optimum of 30 °C and is therefore inefficient in mammalian...identification of FLPe which has a temperature optimum of 37 °C (Buchholz, Angrand, and Stewart 1998)....less efficient than Cre recombinase. FLPe codon optimization resulted in FLPO, which shows similar efficiency...the recombination should only occur at a specific time point? To allow temporal control, ligand regulated...and its synapse should be visualized at the same time from two different plasmids this approach becomes...rearranges these synapses in the living brain over time (Villa et al. 2016). Combing FLP and Cre for additional...
  29. The CRISPR Software Matchmaker: A New Tool for Choosing the Best CRISPR Software for Your Needs

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    Blog Post
    ... the better (Nat. Biotechnol., 2014). Given the timing, it shouldn’t be a surprise that the CRISPR system...software to make sgRNA design accessible to all. At the time I thought there was room for improvement and a year...iterative design; it is caused by not having the time to assess public response; and, it is the stage ...winner, is there something that we can invest our time into learning and extract the most value? This is...and not general opinion. I could spend a lot of time running through each tool in detail, but that is... genomes of any size and are only limited by the time it takes authors to add a genome to the tool’s repertoire...those who are entering sgRNA design for the first time, it is best to choose a tool based on immediate ...
  30. SARS-CoV-2/COVID-19 Detection Methods Based on CRISPR/Cas

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    Blog Post
    ...one of the earlier epicenters of the outbreak ultimately flattening the curve, it has become evident that... reagents and equipment and the long turnaround times, have led researchers to turn to other technologies... Sensitivity:10-100 copies of RNA per microliter Time: ~40 minutes Equipment required: 37°C heat block... developed so far.  A similar method has been optimized to detect the SARS-CoV-2 virus directly using ...milliliter can be detected – in the zeptomolar range Time: ~1 hour Equipment required: 37°C water bath and...microliter of RNA targets in a 40-minute incubation  Time: ~90 minutes Equipment needed: 37°C heat block, ...CREST) Sensitivity: 10 copies of RNA per microliter Time: Not mentioned in the paper, likely approximately...
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