Helping unlock the promise of cellular therapies and regenerative medicines
As cell therapies transition from the lab to patients’ bedsides, ensuring the highest levels of quality and safety is a significant and critical challenge. PeproTech’s PeproGMP® Cytokines help researchers meet that challenge. Consistent with federal
requirements and best practices for cell therapy, gene therapy, and tissue-engineered products for clinical applications, PeproGMP® Cytokines are manufactured and tested in compliance with US FDA GMP (Good Manufacturing Practices) regulations and the ISO 9001 quality management systems standard, without the use of animal-derived materials.
PeproGMP® Cytokines offer safety, purity, and simplified use in ex vivo manufacturing processes, as described in USP (United States Pharmacopeia) Chapter <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products.
GMP Quality GMP FAQs GMP Brochure
|Products currently available for sale include:
|PeproGMP® Recombinant Human FGF-basic (154 a.a.)
PeproGMP® Recombinant Human IL-6
PeproGMP® Recombinant Human IL-3
PeproGMP® Recombinant Human Flt3-Ligand
PeproGMP® Recombinant Human SCF
Customer Service for a quote on our PeproGMP®