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  1. Hot Plasmids - May 2022

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    Blog Post
    ...sequences more efficient and less risky.   Fig. 3: Development of a cleavage-free dCas9-based gene editor... plasmids you need. If you'd ever like to write about a recent plasmid deposit please sign up here. ...
  2. Hot Plasmids - February 2022

    Type
    Blog Post
    ...protein expression and purification. Figure 3: The Penn State Ladder run on SDS-Page gels. A: individually... plasmids you need. If you'd ever like to write about a recent plasmid deposit please sign up here.  ...
  3. 27 Hot Plasmids from 2016

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    Blog Post
    ...and complete screening in just 3 days? Thanks to Tyler Jacks’ lab, this 3-day goal is is now attainable...construction of a so-called “genomically recoded organism” (3) but its portability to other bacterial strains remains... the assembly of TALE repeats into a single-tube, 3 day process by utilizing pre-assembled trimers to ...but be sure to let us know if you'd like to write about your plasmids in a future blog post. No time to ...pooled libraries, but thanks to a deposit from the laboratory of Dr. Ji-Long Liu at Oxford University, we are...you plan to use GMAP for your experiments, think about depositing your new plasmids with Addgene to help...and context-dependent human fitness genes, the laboratory of Jason Moffat at the University of Toronto ...
  4. Plasmids for Endogenous Gene Tagging in Human Cells

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    Blog Post
    ...enter the cells so they can go to work. Figure 3: Inducing the double strand break and introducing ...the Addgene Blog Learn More about Homology Directed Repair Learn More about Non-Homologous End Joining .... For a C-terminal tag, as shown in the example above, we inserted a linker and GFP tag at the end of ... and 1kb of homologous DNA flanking both sides (about 2.7kb total)—is inserted into a plasmid backbone... Plasmids, plasmids everywhere To find out more about gene edited hiPS cell lines generated using the ...line. The editing strategy and design described above can be used to create similar donor plasmids for...microhomology-mediated end-joining (MMEJ). To find out more about gene edited hiPS cell lines generated using these...
  5. Antibodies 101: Affinity Reagents

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    Blog Post
    ...ankyrin repeat proteins. DARPins typically consist of 3-4 repeats, have high specificity and binding affinity... time, when someone speaks about an affinity reagent, they’re talking about a standard antibody: An ~150kD...mutation, allowing diabodies to be used for assembling protein nanostructures. Diabodies readily co-crystalize...for clinical applications, including imaging.  Diabodies are ~60 kDa proteins formed by two Fab fragments...2019). Structural diversity and flexibility of diabodies. Methods. 10.1016/j.ymeth.2018.09.005 Muyldermans...
  6. Career Coaching for Scientists: Why and Where Do I Find One?

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    Blog Post
    ...Always ask for references and follow up with 3-4 to hear about those clients’ experiences. Good coaches will...Individual Development Plan Learn a Little about The Academic Labor Environment from the Future of Research...research.  It helps to spend some time thinking about what your goals are for the coaching relationship...with someone you connect with. Talk to the coach about their “style” and make sure this is a style that...coaching group is Still Point Coaching. One nice thing about a group is that sometimes this offers the option...
  7. Seven Tips for Using LinkedIn as a Scientist

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    Blog Post
    ...either as this also results in a generic invitation. 3) Connect with people you have really talked to The...include a note about where you met IRL (in real life) and perhaps what you talked about (or how good the... this rule, but not that many). I’m asked a lot about requesting connections to complete strangers for...have been able to tell when some start-ups were about to be bought by seeing certain groups of people ...using social media as a scientists Read blog posts about networking ...
  8. Antibodies 101: ELISA (Enzyme-linked Immunosorbent Assay)

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    Blog Post
    ...against the antigen bound to the plate. Figure 3: Overview of using Direct ELISA to quantitatively ...blog Learn about the advantages and disadvantages of using monoclonal antibodies. Read about other techniques... require two different antibodies. As mentioned above, it can also be used to characterize antibodies ...concentration of proteins in an ELISA well As mentioned above, the measurement of the concentration of proteins...
  9. Antibodies 101: Conjugation

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    Blog Post
    ...make up the disulfide bonds between antibody chains. 3) Endogenous carbohydrates added to antibodies post-translationally...Check out our post on Biotinylation to learn more about biotin and its use in molecular biology. Other Conjugates...perfectly blissful, productive lives without thinking about these chemical reactions. After all, there is an...ready to use off the shelf. So why are we talking about this? Even though there are so many commercially...
  10. CRISPR 101: Cas9 vs. The Other Cas(s)

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    Blog Post
    ...endonuclease of a class 2 CRISPR-Cas system. Cell, 163(3): 759-771 (2015). 10.1016/j.cell.2015.09.038 Harrington... is smaller than the traditional SpCas9 enzyme (about a third of the size) and does not require a tracrRNA...Cas12a to further optimize it for therapeutic and laboratory usage. Fast facts – PAM requirement: TTN or ... the lack of collateral cleavage). You can read about Cas7-11 in our blog post on its development and ...
Showing: 411 - 420 of 521 results