Immunostaining of Caenorhabditis elegans
Corresponding Organization :
Other organizations : Emory University
Variable analysis
- Treatment with respective primary antibody overnight
- Treatment with secondary antibody for 4 h at room temperature
- H3K4me3 levels
- H3K4me2 levels
- GFP levels
- TRA-1 levels
- Worm dissection and processing as described before (14, 31)
- Concentration of primary antibodies: Rabbit anti-H3K4me3 (1:1000), Mouse monoclonal antibody against H3K4me2 (CMA303; 1:20), Mouse monoclonal antibody against GFP (1:500), Rabbit anti-TRA-1 (1:100)
- Concentration of secondary antibodies: goat anti-mouse IgG (Alexafluor 488), goat anti-rabbit IgG (Alexafluor 594), donkey anti-rabbit IgG (Alexafluor 488), donkey anti-mouse IgG (Alexafluor 594) at 1:500 dilution
- DAPI (2 μg/μl) used to counter-stain DNA
- Worms mounted in anti-fade reagent (Prolong Gold)
- Imaging using Leica DMRXA fluorescence microscope and Simple PCI software (Hamamatsu Photonics)
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!