Whole mount staining is the staining of small pieces of tissue, usually embryos, without sectioning onto slides first. This is often used on embryos by stem cell and embryonic development researchers and also neuroscientists who are able to stain the whole embryos at various stages to follow the expression of target proteins through the development of the animal.
Whole mount staining is very similar to immunocytochemistry (ICC) or staining of cryosections. If an antibody has been used successfully on cryosections (IHC-Fr - this does not including paraffin embedded sections), then the antibody should work for a whole mount embryo. The difference being that the sample being stained is much larger, and thicker, than a normal section on a slide. Therefore, incubations for fixative, blocking buffer, antibody, wash buffer, permeabilization and substrate color development will need to be much longer to allow for permeabilization right into the centre of the sample. Researchers use different times, but the details in these procedures provide a guideline for optimizing the experiment at these stages if necessary.
- Whole mount fluorescent immunohistochemistry protocol
- Chick or mouse whole mount immunohistochemistry protocol
- Drosophila whole mount immunohistochemistry protocol
- Zebrafish whole mount immunohistochemistry protocol
- Whole mount troubleshooting tips
An important note on fixation:
Whichever fixative has been successfully used in IHC-Fr with the antibody you have chosen should be suitable for whole mount. However, most researchers use 4% paraformaldehyde (PFA). Although this concentration of PFA is very low, this has to be left on for a long period of time on whole mount samples to allow for permeabilization to the centre of the sample. Therefore, this will not be suitable for all antibodies, as the protein cross linking formed by the fixative may block access of the antibody to the epitope. Normally, in IHC-P, you could perform antigen retrieval. This is not possible on embryo samples as the heating procedure would destroy the sample. If PFA fixation does not work for the whole mount tissue, then there is a possibility the antibody is sensitive to the protein crosslinking, and you will require another fixative. Methanol is a popular second choice of fixative when optimizing whole mount procedures.
Zebrafish embryo fixation and preparation requires extra steps to fix and permeabilize to ensure the egg membrane is permeabilized. See Zebrafish whole mount protocol for details.
Some researchers view and obtain images of embryos as they are. The whole embryo can be imaged while floating in glycerol buffer in a petridish, before mounting. If small enough, the whole embryo can be mounted in glycerol before setting in a coverslip. In this case, grease should be used around the corner of the coverslip to help keep it in place and prevent damage to the coverslip when using the microscope. However, they can also be set in geletin and sectioned if it is difficult to obtain a clear view of the staining through the whole embryo (particularly at larger late embryo stages or larger tissue samples).
If immunofluoresent labeling is used, then confocal microscopy can be a useful tool to scan through the embryo, rather than sectioning the whole embryo onto separate slides after staining.
Choosing the age of the embryo:
This is important as the embryo grows, it will become too large to stain. The various reagents, including fixative, antibody and developing solution will not be able to permeate to the centre of the sample, and the number of stained cells will make obtaining a clear image very difficult. However, larger and older embryos can be dissected into segments before staining if necessary.
- Chicken embryos: up to 6 days
- Mouse embryos: up to 12 days