bob1, on 28 October 2012 - 11:42 PM, said:
That looks like a quite standard protocol, apart from the wash durations, which may be too long and too stringent - you can permeablize in the PT buffer and then do the washes in PBS-T (PBS with 0.1% tween 20).
If you are having significant background you may need to use a different fixative with a the ability to decolourize the cells - this is often glutaraldehyde (instead of formaldehyde) and DMSO based, but I can't remember the specific details or even the name of the solution.
You might be well advised to have a look on IHCworld.com, where there are heaps of protocols and basic explanations of different solutions and techniques.
If you are having significant background you may need to use a different fixative with a the ability to decolourize the cells - this is often glutaraldehyde (instead of formaldehyde) and DMSO based, but I can't remember the specific details or even the name of the solution.
You might be well advised to have a look on IHCworld.com, where there are heaps of protocols and basic explanations of different solutions and techniques.





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