We narrowed to 600 results for: ARL

...the protocol, samples can be expanded to ~4-10x linearly! This expansion physically separates molecules...

...reagents, making it more difficult to detect. A particularly strong absorber at 230 nm is guanidine thiocyanate...

...consistent dilution factors, change pipette tips regularly, and mix samples very well.  Use duplicates or...

..., Zhan C, Malm M, Field R, Turner R, Sellick C, Varley P, Rockberg J, Chotteau V. Small-scale bioreactor...

...robustly, quickly, and simply. We hope that you can similarly apply MXS chaining to your experimental needs....

...transformant. Use young plants: If you transform early, your plants will still have plenty of time to produce...

...transfection (B in the figure above), are in the early stages of development. David Liu’s Lab has demonstrated...

...journal articles. From paper to plasmid Authors regularly indicate that their plasmids are available from...

...difficult it is to trace individual cell’s axons, particularly the two green neurons near the arrows. When ...

...  PCR set-up Setting up colony PCR reactions is nearly identical to preparing a standard PCR reaction:...

...References 1. Buchholz, Ursula J., Stefan Finke, and Karl-Klaus Conzelmann. "Generation of bovine respiratory...

... type of transcription reporting was among the earliest uses of GFP. Fluorescence resonance energy transfer...

...you’ll never know it so don’t miss out on those early kisses. The laundry or dishes can wait. Also, be...

... of encouraging dissent, the next tip may be particularly relevant to you. Elect a devil’s advocate. This...

...they saw indel formation and phenotypic changes as early as 1 week post-injection. Livers from these mice...

...control, the internal control vector, was described earlier. Once you are sure your conditions are conducive...

...reliable primary antibodies for their detection, particularly when antibodies to the POI are non-specific,...

...generating a standard curve of known concentration. We regularly make and validate fresh plasmid standards. We...

...to live in your lab, right? Wrong! While it is clearly a good idea to be diligent in your research, remember...

...our more popular libraries, you might receive a similarly-sized aliquot from an amplification done by Addgene...