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...mouse strains). AAV-PHP.eC, AAV9-X1.1 and AAV1-X1 do not display strain-specific tropism and can be used...choose the best capsid for your cell type. First, do you want to target CNS or PNS? Then consider...

...csRNP method is as simple as doing routine PCR assays. Here is a simple to-do-list to follow when planning...Medicine (CRM), Edinburgh. Most commercial antibodies do not work in pull-down assays: Epitope tagging provides...knock-in efficiency (<2% positive by ICC for the tag) or do not see any cells positive for tag insertion, you...et al. 2018), however, if you have any questions, do not hesitate to contact me at [email protected]...

...you, you may wonder which antibody should I pick? Do I go for the rabbit or the mouse? Is mouse IgG1 better...signal strength (Fig. 1). Monoclonal primaries If you do decide on a monoclonal antibody you may wonder, “...immunoglobulins and reduce the background staining but they do not always eliminate the issue (Lu 1998). Consequently...

...templates for the cloning process. Time spent actually doing the experiments are also generally comparable so...inexpensive DpnI enzyme. Otherwise you let your E. coli do the work for you. Traditional restriction enzyme ...are never any guarantees, some cloning techniques do tip the scales in your favor. For starters, Golden...

...Get your voice out there Here’s one thing you can do today: Sign up for a Twitter account. Check out the...happening. 3) Volunteer – Step into science education Do you aim to reach young people? Try networking with...TED-Ed lesson. 6) Network – Mingle with pros Where do you meet like-minded science communicators? Attend...

...insertions that could compromise function. When we do find mutations, we check to see if they affect the... confirms that these differences are expected and do not affect plasmid function, we will update information... They also differ from the CPS process in that we do not fully sequence all plasmids in the pool but instead...

... at this still relatively small nonprofit. If you do go longer than a few days without getting a response...particularly when it comes to technical questions. BUT, I do believe that scientists who contact customer service...Our Frequently Asked Questions Pages Learn What to Do with Your Plasmids Once You Recieve Them Get Help...

...tell, we don’t really know what circRNAs do yet or how they do it. Of course, No conference would be complete...work done by the ENCODE project consortium did not do a good job of seeing tRNAs because they contain “...

...environment without sacrificing performance or quality. To do this, we can use the ACT label, which is an eco-nutrition...approach to lab waste is something we all need to do. Remember, it was only 50 years ago that we routinely...

... SITN, we discuss some of the many things you can do start your own science communication student group...get more involved with your local community. What do Vini and Amy say is the quickest way to get things...

...views for the month of September! Historically we do better in September than in the summer months, but...phages are viruses that infect bacteria and that can do so with exquisite specificity (check out our interview...

...and easier to use than genomic libraries, but they do not contain as much regulatory information. To make... Apply library Apply selection, most cells die or do not pass selection (in the case of a reporter) Sort... screen, the goal is to identify those cells that do not survive the selection mechanism. You’ll transduce...

...influenced by temporally ordered biochemical events. How do RSMs work? The state of an RSM is defined by the ...live, intact cells; the sequencing and qPCR methods do not. How might one implement RSMs? In our study (...that correspond to the desired inputs. Such sensors do not necessarily have to be based on transcriptional...that best suits your application. How efficiently do RSMs work? We tested a two-input (ATc and Ara) RSM...

... Plasmid Description Gene/Insert PI Return to top Do you have suggestions for other plasmids that should...

...prepared me that those challenges would be from doing a remote internship during a pandemic. Before I ...role in the company. One of the things I wanted to do was create content that was unique but also brand...

... job descriptions clearly describe that the roles do not involve bench research. I am always surprised... 5) Apply for the job as requested in the posting Do this online and/or via email exactly as the job posting...

...received over 2,000 entries. Do you mix your passion for art and science? Do you look for the beauty in ...

...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...

...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 ...

... on the inside of the cell. However, assuming you do need to permeabilize, you have a few options for ...organellar membranes. Created with BioRender.   How do I choose?! Ok, so now you know some of the possible...possible types of fixatives or permeabilizers, but how do you decide which ones to use? Here are some tips ...