Hi!
My task was to form EB from mouse ipsc (2A-EGFPTg-3F) and from there, someone will use the EBs to differentiate to hematopoeitic cells. But, when we checked it, EBs were formed but they were too small, too small that they couldnt be used for differentiation.
What could have been the cause for this? and how can I improve it?
Thanks a lot!
Help needed- EBs were too small for differentiation
Started by minerva_29, Oct 12 2011 05:09 AM
stem cells EB formation
3 replies to this topic
#1
Posted 12 October 2011 - 05:09 AM
#2
Posted 12 October 2011 - 10:11 PM
Dear,
Feed them regularly.
Which tissue culture plates are you using for EBs formation?
Feed them regularly.
Which tissue culture plates are you using for EBs formation?
#3
Posted 12 October 2011 - 10:54 PM
Thanks!
I used the round bottom low cell bindin 96 well plate. i seeded 1000 cells in 1row and 3000 cells in the 2nd row. after 2 days, i added 80uL of EB medium. 3 days later i changed the medium.
I used the round bottom low cell bindin 96 well plate. i seeded 1000 cells in 1row and 3000 cells in the 2nd row. after 2 days, i added 80uL of EB medium. 3 days later i changed the medium.
#4
Posted 19 March 2012 - 06:47 AM
Try to seed more cells and use larger plates, the cells will clump together as time goes.
Also tagged with one or more of these keywords: stem cells, EB formation
Protocols and Techniques Forums →
Stem Cell →
rtPCR stem cell signalling array from quiagen- has anybody experience?Started by Guest_Slu_* , 31 Oct 2012 |
|
|
||
Protocols and Techniques Forums →
Stem Cell →
detection of mesenchymal stem cells in cancer tissue sampleStarted by Guest_Shivali Duggal_* , 09 Jul 2012 |
|
|
||
Protocols and Techniques Forums →
Stem Cell →
differentiating neurons detaching from plateStarted by Guest_jlolsen_* , 09 Apr 2012 |
|
|
||
Protocols and Techniques Forums →
Cell Biology →
Carrier protein concentrationStarted by Guest_saawan_* , 28 Feb 2012 |
|
|













