hi,everyone
I'd like to observe the cells using the Laser Scanning Confocal
Microscopy (LSCM), but I do not know how to dispose my cells before the
observation, that is to say, I want to know how to fix my cells effectively
so that the detectedcells could be observed much more truely.
Would you mind sharing with me if you know about it happenly?
Thanks a lot!
cell fixation
Started by geness, Oct 15 2004 06:48 AM
5 replies to this topic
#1
Posted 15 October 2004 - 06:48 AM
#2
Posted 17 October 2004 - 04:25 AM
Hi
What cells are you using?
we fix bacteria in 4% formaldehyde for 1 to 24 hours, works just fine for LSCM
What cells are you using?
we fix bacteria in 4% formaldehyde for 1 to 24 hours, works just fine for LSCM
#3
Posted 18 October 2004 - 02:31 AM
hi,leahf
The cells used are HEK 293T cell lines.
The cells used are HEK 293T cell lines.
#4
Posted 03 December 2004 - 01:54 AM
hi
u can use PFA 3% + gluta 0.5% 10 min at 37°C
rince with PBS or Tris 3*10min
u can store them 1 month at 4°C.
u can use PFA 3% + gluta 0.5% 10 min at 37°C
rince with PBS or Tris 3*10min
u can store them 1 month at 4°C.
#5
Posted 03 December 2004 - 09:31 AM
Hi Geness
4 % paraformaldehyde in PBS will good for fixing cells.
Anil
4 % paraformaldehyde in PBS will good for fixing cells.
Anil
#6
Posted 09 January 2005 - 06:20 AM
hi,
Thanks a lot!
I believed that 4 % paraformaldehyde in PBS is good for fixing mammalian
cells.
But I'd like to know where I could get the manufacturer's instruction
about detailed fixing cells for Confocal detection.
If you know,would you mind sharing with me ? Thank you very much!
Thanks a lot!
I believed that 4 % paraformaldehyde in PBS is good for fixing mammalian
cells.
But I'd like to know where I could get the manufacturer's instruction
about detailed fixing cells for Confocal detection.
If you know,would you mind sharing with me ? Thank you very much!














