Problems with fixation?
Posted 19 March 2012 - 02:57 AM
I write to ask you for some suggestions. I explain you my problem: I use to fix my cells and then to perform an antibody staining. The fixation protocol involves the next steps:
- PFA 4%, 15min at room temp
- Triton 0.5% 5min at room temp
- (after 2 washing steps) BSA 0.4% 30min at room temp
My problem is that the FSC signal I usually get from my samples is not homogeneous at all, the signal can be really different from one sample to the other one (even 100% difference), and this reflects also on the signal coming from the antibody.
I guess this problem could be due to some bugs in the fixation, but I'm not that expert at all.
Do you have some useful clues/ tips?
Thank you in advance!
Posted 19 March 2012 - 03:27 AM
Posted 19 March 2012 - 05:05 AM
thanks for answering. Unfortunately I need to fix my cells. Perhaps I could try to reduce the incubation time, but if aggregates are produced I should be able to see them if I look at my cells at the microscope, isn't it? Sometimes I look at them just to check that the staining worked, and in fact it seems to work fairly well, and I don't see a lot of aggregates.
What do you think about this?
Posted 19 March 2012 - 05:09 AM
Just for information, I use to centrifuge my cells (CHO) at 200g.
Posted 19 March 2012 - 11:02 AM
Il dort. Quoique le sort fût pour lui bien étrange,
Il vivait. Il mourut quand il n'eut plus son ange;
La chose simplement d'elle-même arriva,
Comme la nuit se fait lorsque le jour s'en va.
Posted 19 March 2012 - 06:04 PM
Have you ever tried the Cytofix/Cytoperm reagent (BD) ? I use it to permeabilize and fix my cells before flow cytometry.
I use the intracellular staining buffers (that are part of the foxp3 kit, but I order them separately- I think they are essentially the same as the cytofix/cytoperm) and I love them.
Before using them I had so many problems with my flow, but now nothing.
Honestly, do yourself a favour and just buy the stuff from BD!
The extra expense will be well worth it compared to your time and energy in making the reagents you currently use (esp. the PFA, jeez I hate making that!!), and the time you are wasting trying to optimise your fixation.
Posted 20 March 2012 - 09:35 AM
Posted 03 April 2012 - 10:48 AM
a collegue in our lab just discovered the same problem! he found out that if you fix your cells with ethanol, the FSC signal is MUCH more stable! the only problem is, that you must check if then your antibody staining still works fine.