...Agrobacterium strains see Weigel and Glazebrook, 2002. Tips: Do a colony PCR on your agrobacterium: Getting a transformant...

...single molecules - something researchers often want to do at neuronal synapses for instance. Also these tags...

...systemic delivery of high doses of vectors are needed. Additionally, AAVs do not integrate in the host...

...your sample names and guide sequences, and ICE will do the rest. There are no parameters that need optimizing...

...high-quality data for our DNA-based reagents. Not only do we extract as much information as possible from depositing...

...explore. I hope that this brief guide can help you do just that. Good luck, and always keep going. Appendix...

...was actually engineered to target the CNS. How well do these AAVs transduce the CNS and PNS? Both plasmids...from. Additionally, AAV.PHP.eB was used at a lower dose than it’s parent AAV.PHP.B: 1x1011 vs 1x1012 viral...blue (RGB) fluorescent protein (4a-c). When high doses of this viral cocktail are injected, by chance lots...the two green neurons near the arrows. When lower doses of virus are used in order to decrease the number...AAV.PHP.eB capsid. Both viruses were IV injected at a dose of 1x1011 vg per mouse and the level of transduction...AAV.PHP.S capsid. Both viruses were IV injected at a dose of 1x1012 vg per mouse and the level of transduction...-off transactivator (tTA), is injected at a high dose to maximize the number of cells that are labeled...

... spin columns you need to complete your research. Do you know of other nucleic acid purification methods...

...in the biosynthetic pathway. Why plant scientists do transient leaf transformations The development of...

...Hoshino and Fujii, 2009). Other forms of enChIP, that do not use dCas9, require Zinc-finger or TAL proteins...

...become resistant to? CRISPR may provide a method for doing just that. While challenges remain in the delivery...

...virus (similar to lentiviral vectors) because they do not encode all of the necessary viral proteins. Minigenome...

...protein molecules fail to correctly fold? Misfolded FPs do not fluoresce. A dark population is not readily apparent...

...share your protocols with other groups. What apps do you use to improve your lab productivity? As this...

... list is a great place to start, the tables above do not delve into the tissue or development-specific...

...little excess gel around the band as possible. To do so, it is often important to take the excised band... about DNA quantification here . Tips and FAQ How do you get better resolution of bands? A couple simple...gel comb; or c) loading less DNA in the well. How do you get better separation of bands? If you have similarly...

... regions communicate with each other and how they do it (i.e. where the signals come from and what implications...migrates through neurons where it can replicate and by doing so spread across several synaptic connections (Ugolini...

...strategy, sometimes it cannot be avoided. If you do have to do so, there is no way to control which orientation...vector backbone and therefore the only thing left to do is identify the clone(s) in which the insert is in...

...bacteria containing that plasmid from bacteria that do not contain it by artificial selection (i.e. growing...growth (bottom) Loosely close the cap on the bottle (do NOT close all the way or the bottle may explode!)...concentration ( see table below ). Note: If you intend to do a mini-prep you will usually want to start 2 mL in...

...wear it the whole time you are working in the lab. Do not eat, drink, chew gum, or apply makeup in the ...way. It is the easiest way to ensure that you’re doing your work in the safest way possible. Protecting...this SOP in another location, please note that you do so at your own risk; you should ensure that any local...