We narrowed to 770 results for: Dos;

1. Creating accessible biology activities in schools with BioBits

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   ...also see how fun biology can be! What can BioBits do for you? We initially developed the BioBits kit to...

2. Identifying Sequence Elements with SnapGene's Feature Database

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   ...For every task, we envision what the user wants to do and make the path to accomplishing their goals as...

3. Trading Spaces - Visiting Scientist Edition

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   ...third parties or your home institute. Discuss rights Do you expect to generate data that will contribute ...

4. Antibodies 101: Epitope Tags

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   ...- but for many other proteins, quality antibodies do not exist, or they don’t exist for a specific application...

5. Antibodies 101: Chimeric Antibodies

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   ...indirectly probed simultaneously on the sample. What to do?  If you’ve ever found yourself facing a similar ...

6. The MTA at Addgene

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   ...transparency in an otherwise messy process.  And you do have options for the terms you want to share your...

7. Visualizing Translation at the Single Molecule Level

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   ...experiments, it’s important to verify that these changes do not impact translation rate, as the authors of these...

8. Fluorescent Protein Travel Awards - FLiPs and Fluorescent Protein Biosensors

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   ...oligomerize when exposed to ultraviolet light. To do so, she generated fusion proteins in which Dronpa...

9. Viral Genome Sequencing - A One Stop Shop for AAV Identity and Serotype Confirmation

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   ...main tenets of our quality control (QC) mantra is to do our utmost to ensure that scientists are receiving...

10. Hot Plasmids - September 2019 - CRISPR, Auxin Inducible Degradation, MerMAID Channelrhodopsins, and Genome Looping

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    ...eukaryotes don’t naturally have this response, they do contain the specific ubiquitin ligase pathway needed...

11. Scientific Peer-review: Providing Critical and Kind Feedback and Advocating for Open Science

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    ...read of the paper is much more detailed. I prefer to do it on another day - preferably the following morning...

12. Optimizing Donor DNA for Enhanced CRISPR Genome Editing

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    ...We began our research with a simple question: how do Cas9 and sgRNA interact with and dissociate from ...

13. Don’t Wait To Launch Your Health Science Startup

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    ...think of entrepreneurship in the 21st century, who do you think of?  Your mind is likely drawn to the Mark...

14. Choosing Your Fluorescent Proteins for Multi-Color Imaging

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    ...multiple fluorescently tagged species simultaneously. To do so with fluorescent protein labels requires multiple...

15. Plasmids 101: How to Verify Your Plasmid Using a Restriction Digest Analysis

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    ...vector by excising the insert from the backbone. To do this, you'll use enzymes with restriction sites that...

16. Advice for Moving Into Sales After Your Science Postdoc

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    ...would would make a good fit for me?" Whatever would I do next and what options lie ahead of me? Like a considerable...

17. History of CRISPR Cas - A tale of survival and evolution

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    ...Guide or find CRISPR/Cas plasmids for your research. Do you have a cool idea or application that involves...

18. Fluorescent Proteins 101: Photoactivatable Fluorescent Proteins

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    ...conventional FPs for super-resolution imaging, they still do not emit the large number of photons achievable with...use in yeast, as parts of biosenors, and much more. Do you have a favorite use for PA-FPs? Let us know in...

19. Plasmids 101: Inducible Promoters

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    ... their low leakiness. Inducibility level How much do you want to induce transcription of your target gene...

20. Flow Cytometry Readouts: Yes, No, and Everything in Between

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    ...the histogram plots look a bit different than they do for yes-no readouts.      Figure 4: A histogram...