We narrowed to 750 results for: Dos

...Accuracy needed Do you need to call exact copy numbers or just general trends? How confident do you need to...researchers can use to quantify said copies. They do so using copy number variation (CNV) assays. There...

...blue to ultraviolet light, whereas chromoproteins do not fluoresce at all or fluoresce at very low levels...identified in sea anemone (Chan et al., 2006). Why do these organisms have chromoproteins? One reason may... mutation and excision of the vector backbone. To do this, rhamnose is added which induces expression ...

...and tell your audience just that. Explain what you do know about a related topic, and let them know while...overwhelming than stepping into a sea of posters – where do you begin? Design a game plan Prior to attending ...poster you want to know more about? Interested in doing a postdoc in a presenter’s lab? Want to collaborate...

...it. Biotech companies are known to have tools that do this internally, but they are not available publicly...advised, there is little detail published on how to do it best. Scientists are typically advised to mutate...boosted our productivity in the Biohub. We hope it will do the same for you. Send us your questions or comments...

...which are doing important work in our microbiomes. Given that viruses are everywhere and doing everything...we try to use them in an experiment and they don't do anything. Viruses are complicated and they perform...

...before using them to screen colonies. The best way to do this is by using your vector with and without an ...clones for later use. There are a few ways you can do this. If you are going to complete your colony PCR...Additional Resources on the Addgene Blog Learn to do Restriction Cloning Try SLIC cloning Learn about ...

...times).     I guess it's cool to be popular, but how do I know if a plasmid is actually useful to me? Plasmid... I want to use this plasmid in a publication, how do I know who to acknowledge? Depositing lab: The name...Our Walkthrough of the Deposit Process Learn How We Do Quality Control at Addgene Resources on Addgene....

...deposit had already moved on to their next position. We do routinely review deposits that are left in the hold...materials the way we will with journal articles. But we do encourage you to consider sharing them openly as ...

...shadowing members of my team to learn what I was to do for my time at Addgene. This training prepared me...where each team gives a presentation on what they do and how it relates to other teams at the company....

...disease. Figure 1: Scientists are continuing to do essential research into COVID-19 (like here at Addgene...boundaries. To be able to beat this virus, we will need to do the same with science,” said Guillaume Bourque, a...

...questions about scientists on Twitter: who are they? What do they share? And how they are connected? Here are ... (left), life (center), and physical (right). How do you use Twitter as a scientist? If you don’t use ...

...at Addgene. You are the reason we’re able to do what we do!          Special Thanks Trophies and engraving...

...publications relevant to your research interests. We do this by promoting citation, supporting sophisticated...can put straight into your reference section. Why do this? Not only does citing plasmids from Addgene ...

...education? Let us know in the comments section below! Do you know of a society or event which would benefit...While we are not able to help with every request, we do aim to support events and scientific community activities...

...using microfluidic devices. Addgene: What other uses do you foresee for this tool? Howarth: Polyproteins ...infected with malaria or other parasites. Addgene: Do you have any particular tips or tricks for those ...

...experiments and why? What techniques and skills do you need to use to reach these milestones? Can you...milestones along the way so that you don't get stuck doing the same experiment for too long. Keep evaluating...

... yourself with this passion. “Love what you are doing!” It helps when the time comes to work with full...become more aware of careers outside of academia. How do PIs assist their mentees who have goals outside of...

...comes from. Then consider the following questions: Do you need polyclonal or monoclonal antibodies? Will...direct or indirect detection method? If indirect, do you already have secondary antibodies available in...have identical features and epitopes, to ensure you do not validate the same antibody multiple times. You...antibodies will also have a source species. What conjugate do you want to use? Most secondary antibodies will be...buy small aliquots of many different antibodies and do batch validation up front rather than risk delaying...

...move on to your downstream application — but wait! Do you know how much plasmid DNA you have or how pure...absorbance readings are inherently more variable. If you do need to work with dilute samples:  Take multiple...the references we have provided below. And if you do have trouble with contamination, feel free to check...

...CRISPR could cut DNA, the second generation could do base editing, and with the third generation came ...? The AbuGoot lab realized that they could likely do it using Prime editing alongside some creative (and...represent a major step forward for what the field can do.    References and Resources References  Özcan A...