Visualizing Fluorescent Proteins in Cellular Processes
Corresponding Organization :
Other organizations : Universität Ulm, Orthopaedic Research, University Hospital Ulm
Variable analysis
- Microscope used to acquire images (Leica M205FA stereo microscope, Leica SP8 confocal microscope, Zeiss AxioObserver 7 with Apotome)
- Live fluorescence of fluorescent proteins
- Optical sections obtained with microscopes
- Microscope settings and processing using Fiji software
- No positive or negative controls were explicitly mentioned.
Annotations
Based on most similar protocols
As authors may omit details in methods from publication, our AI will look for missing critical information across the 5 most similar protocols.
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required
Revolutionizing how scientists
search and build protocols!