Many thanks for help.
Human Macrophage cell line - quick help please
Started by Fred-33, Sep 08 2004 03:38 AM
4 replies to this topic
#1
Posted 08 September 2004 - 03:38 AM
Many thanks for help.
#2
Posted 08 September 2004 - 06:44 AM
I found my answer on atcc site
here are some useful lines from spleen ant monocytes/macrophages
HB-8902
CRL-9850
CRL-9852
CRL-9853
CRL-9854
CRL-9855
CRL-9856
here are some useful lines from spleen ant monocytes/macrophages
HB-8902
CRL-9850
CRL-9852
CRL-9853
CRL-9854
CRL-9855
CRL-9856
#3
Posted 14 November 2004 - 02:03 PM
Fred-33, on Sep 8 2004, 07:44 AM, said:
I found my answer on atcc site
here are some useful lines from spleen ant monocytes/macrophages
HB-8902
CRL-9850
CRL-9852
CRL-9853
CRL-9854
CRL-9855
CRL-9856
here are some useful lines from spleen ant monocytes/macrophages
HB-8902
CRL-9850
CRL-9852
CRL-9853
CRL-9854
CRL-9855
CRL-9856
#4
Posted 28 January 2009 - 02:01 PM
I have just started culturing THP-1 cells.
After sub-culturing, I wanted to freeze down some of these cells. I froze a vial of cells with my normal freezing media (2x, 20% DMSO and 80% FBS). When I thawed the cells they were viable. After 48h the cells had switched from being in suspension to becoming adherent.
Is this from the DMSO?
Should I use glycerol to cryopreserve instead?
After sub-culturing, I wanted to freeze down some of these cells. I froze a vial of cells with my normal freezing media (2x, 20% DMSO and 80% FBS). When I thawed the cells they were viable. After 48h the cells had switched from being in suspension to becoming adherent.
Is this from the DMSO?
Should I use glycerol to cryopreserve instead?
#5
Posted 03 February 2009 - 06:58 AM
emilydeanna, on Jan 28 2009, 11:01 PM, said:
I have just started culturing THP-1 cells.
After sub-culturing, I wanted to freeze down some of these cells. I froze a vial of cells with my normal freezing media (2x, 20% DMSO and 80% FBS). When I thawed the cells they were viable. After 48h the cells had switched from being in suspension to becoming adherent.
Is this from the DMSO?
Should I use glycerol to cryopreserve instead?
After sub-culturing, I wanted to freeze down some of these cells. I froze a vial of cells with my normal freezing media (2x, 20% DMSO and 80% FBS). When I thawed the cells they were viable. After 48h the cells had switched from being in suspension to becoming adherent.
Is this from the DMSO?
Should I use glycerol to cryopreserve instead?
Yes I have found that DMSO causes my cells to differentiate. 20% DMSO is very high - 10% is enough. I now use a special freezing medium for my cells as i had a huge problem with differentiation. When you thaw your cells you should spin them down at a low speed and remove the freezing medium to remove the DMSO.













