SCC058
FibroGRO® Xeno-Free Human Foreskin Fibroblasts
The FibroGRO Xeno-Free Human Foreskin Fibroblasts are derived from normal human foreskin & have been isolated & manufactured under xeno-free conditions.
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About This Item
biological source
human foreskin (fibroblasts)
Quality Level
packaging
pkg of 1 kit
manufacturer/tradename
Chemicon®
FibroGRO®
Millipore
morphology
(endothelial)
technique(s)
cell culture | mammalian: suitable
cell culture | stem cell: suitable
shipped in
liquid nitrogen
General description
Application
Stem Cell Research
Biochem/physiol Actions
Preparation Note
Analysis Note
Other Notes
Legal Information
Disclaimer
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Articles
The Simplicon™ RNA Reprogramming Technology is a next generation reprogramming system that uses a single synthetic, polycistronic self-replicating RNA strand engineered to mimic cellular RNA to generate human iPS cells.
Fibroblast growth factors (FGFs) regulate developmental pathways and mesoderm/ectoderm patterning in early embryonic development.
Protocols
Stem cell reprogramming protocols to generate human induced pluripotent stem cells (iPSCs) including viral and non-viral RNA based methods.
Related Content
Dual SMAD inhibition is a well-established method to derive neural progenitor cells from both human ES and iPS cells. This protocol uses two SMAD inhibitors, Noggin and SB431542, to drive the rapid differentiation of ES/iPS cells into a highly enriched population of NPCs. Noggin acts as a BMP inhibitor and SB431542 inhibits the Lefty/Activin/TGFβ pathways by blocking the phosphorylation of ALK4, ALK5, and ALK7 receptors. In an effort to make a more defined and optimized neuronal differentiation protocol, Li and colleagues modified the original protocol to establish a completely small molecule-based differentiation method, which relies on three small molecules to inhibit GSK-3β (CHIR99021), TGFβ (SB431542), and Notch (compound E) signaling pathways, along with human LIF3. This new small molecule-based neural differentiation protocol increased neural differentiation kinetics and allowed the derivation of truly multipotent neural stem cells that respond to regional patterning cues specifying forebrain, midbrain, and hindbrain neural and glial subtypes.
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