"stem cell cultivation" is a correct and usable phrase in written English.
It refers to the process of growing and multiplying stem cells in a controlled environment. Example: "The lab is focused on researching new techniques for stem cell cultivation in order to improve treatments for various diseases."
A variety of bioreactors for cell cultivation exist and can be readily adapted for stem cell cultivation and differentiation.
The calculated percentages exemplify the potential of feeder cell contaminations during stem cell cultivation and differentiation and might vary considerably dependent on seeding conditions.
The aim of the present study was to establish a method that provides optimal conditions for stem cell cultivation, such as the co-cultivation of feeder and stem cells during the proliferative phase, and at the same time allows for the analysis and transplantation of feeder free stem cells.
Media exchange and perfusion strategies have been used previously for adult stem cell cultivation [ 3, 9] and human embryoid bodies [ 13].
The media exchange mode overcame these drawbacks, being the most efficient strategy to enhance undifferentiated stem cell cultivation, as shown by the higher cell densities and higher culture viability obtained throughout the cultivation time.
These include systems for investigating proliferation and differentiation of metacestode vesicles under host cell free conditions [ 18] as well as a parasite stem cell cultivation system that closely mimics the metamorphic transition of the oncosphere towards the metacestode [ 19, 20].
Inducing the osteogenic differentiation caused as expected, the decreasing of cell number after 4 and 12 days of cultivation by comparison with DF stem cells cultivated with stem cells medium but with no statistical differences.
This study develops porcine platelet-rich plasma (P-PRP) as a FBS substitute for human mesenchymal stem cell (hMSC) cultivation.
Stem cell selective cultivation conditions for JLO-1 have been described in our previous study [ 18].
In this study, we describe a novel in vitro cell culture system for derivation of urothelial cells from murine embryonic stem cells (ESCs) following cultivation on collagen matrices in the presence all trans retinoic acid (RA).
For this aim, there exist perfusion bioreactors for culturing encapsulated stem cells and those for cell cultivation on 3D scaffolds.
