Human embryonic stem cells (hESC) are expected to provide revolutionary therapeutic applications and drug discovery technologies. In order for this to be achieved a reproducible, defined animal component free culture system is required for the scale-up production of undifferentiated hESC. In this work we have investigated the applicability of a recombinantly produced domain of human vitronectin as an extracellular matrix alternative to the common standards Geltrex (TM) or Matrigel (TM). In addition we have validated an ascorbate free media capable of supporting CD30(low) populations of hESC through a multi-factorial analysis of bFGF and Activin A. The recombinant vitronectin domain combined with the ascorbate free media were capable of supp...
Current feeder-free culture systems employing undefined Matrigel are still more effective in maintai...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Maintenance and differentiation of human pluripotent stem cells (hPSCs) usually requires culture on ...
Defined growth conditions are essential for many applications of human embryonic stem cells (hESC). ...
Human embryonic stem cells (hESCs) are pluripotent cells that have the potential to differentiate in...
In human pluripotent stem cell (hPSC) research and applications, the need for a culture system devoi...
The optimization of defi ned growth conditions is necessary for the development of clinical applicat...
This unit describes the routine maintenance and expansion of undifferentiated human embryonic stem c...
Traditionally, undifferentiated human embryonic stem cells (hESCs) are maintained on mouse embryonic...
Human Embryonic Stem (hES) cells will potentially have important applications inregenerative medicin...
<div><p>Here, we introduce a new serum-free defined medium (SPM) that supports the cultivation of hu...
Traditionally, human embryonic stem cells (hESCs) are cultured on inactivated live feeder cells. For...
Here, we introduce a new serum-free defined medium (SPM) that supports the cultivation of human plur...
The evolution of "humanized" (i.e., free of animal sourced reagents) and ultimately chemically defin...
Current feeder-free culture systems employing undefined Matrigel are still more effective in maintai...
Current feeder-free culture systems employing undefined Matrigel are still more effective in maintai...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Maintenance and differentiation of human pluripotent stem cells (hPSCs) usually requires culture on ...
Defined growth conditions are essential for many applications of human embryonic stem cells (hESC). ...
Human embryonic stem cells (hESCs) are pluripotent cells that have the potential to differentiate in...
In human pluripotent stem cell (hPSC) research and applications, the need for a culture system devoi...
The optimization of defi ned growth conditions is necessary for the development of clinical applicat...
This unit describes the routine maintenance and expansion of undifferentiated human embryonic stem c...
Traditionally, undifferentiated human embryonic stem cells (hESCs) are maintained on mouse embryonic...
Human Embryonic Stem (hES) cells will potentially have important applications inregenerative medicin...
<div><p>Here, we introduce a new serum-free defined medium (SPM) that supports the cultivation of hu...
Traditionally, human embryonic stem cells (hESCs) are cultured on inactivated live feeder cells. For...
Here, we introduce a new serum-free defined medium (SPM) that supports the cultivation of human plur...
The evolution of "humanized" (i.e., free of animal sourced reagents) and ultimately chemically defin...
Current feeder-free culture systems employing undefined Matrigel are still more effective in maintai...
Current feeder-free culture systems employing undefined Matrigel are still more effective in maintai...
which permits unrestricted use, distribution, and reproduction in any medium, provided the original ...
Maintenance and differentiation of human pluripotent stem cells (hPSCs) usually requires culture on ...