Cellartis DEF-CS 500 Xeno-Free Culture Medium · Maintains pluripotency and stable karyotype in a 2D non-colony monolayer culture · Ideal for maintenance of undifferentiated pluripotent cells and scale-up to therapeutically relevant cell numbers · Fully compatible with the GMP-grade version for a seamless transition to the clinic Cellartis DEF-CS 500 Xeno-Free 3D Spheroid Culture Medium · Pluripotent cells in the spheroids retain full differentiation potential and stable karyotype · Produces 5 × 109 cells in a 1 L bioreactor within 3–4 passages · Provides a distinct advantage for scale-up to therapeutically relevant cell numbers Cellartis DEF-CS 500 Xeno-Free GMP Grade Basal Medium (Prototype) · Optimized for small- or large-scale production of pluripotent cells for downstream use in clinical research settings · Manufactured as a quality-assured product, according to the guidelines for GMP for investigational products · Rigorous manufacturing standards ensure quality and consistency; all materials are of clinical quality, with traceable production processes
■ 产品应用
· Culturing human iPS cells in completely xeno-free conditions for preclinical studies.
■ 产品目录
Code No.
Product
Size
Y30045
Cellartis® DEF-CS™ 500 Xeno-Free Culture Medium w/o antibiotics
1 kit
Y30042
Cellartis® DEF-CS™ 500 Xeno-Free Additives
1 kit
Y30046
Cellartis® DEF-CS™ 500 Xeno-Free Basal Medium w/o antibiotics
500 ml
Code No.
Product
Size
Y30047
Cellartis® DEF-CS™500 Xeno-Free 3D Spheroid Culture Medium w/o antibiotics
1 kit
Y30046
Cellartis® DEF-CS™ 500 Xeno-Free Basal Medium w/o antibiotics
500 ml
Y30048
Cellartis® DEF-CS™500 Xeno-Free 3D Spheroid Additives
1 kit
Code No.
Product
Size
Y30071
Cellartis® DEF-CS™ 500 Xeno-Free GMP Grade Basal Medium (Prototype)
500 ml
■ 关联产品
Code No.
Product
Size
T303
iMatrix-511
2 × 175 μg
■ 产品详情请点击
Y30045: Y30047: Y30071:
High-quality hiPS cell aggregates grown with Cellartis DEF-CS 500 Xeno-Free 3D Spheroid Culture Medium in stirred tank bioreactors (in perfusion mode). hiPS cell aggregates grown under 4% O2 perfusion conditions were sequentially passaged three times by mechanical disruption (protocol adapted from Otsuji et al. 2014); cells were counted at passage on days 4 and 7, and at the final time point on day 11, to determine the expansion factor relative to the initial seeding number.
High-quality hiPS cell aggregates were grown with Cellartis DEF-CS 500 Xeno-Free 3D Spheroid Culture Medium in stirred tank bioreactors (in perfusion mode). After expansion of hiPS cells as aggregates, cells were harvested on day 4 and expression of OCT4, SSEA-4, TRA-1-60 (pluripotency markers) and SSEA-1 and SOX17 (differentiation markers) was analyzed by immunostaining.