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You searched for "chemically defined%3A%3A%3A%3A"

362 Documents found
  • 3D Natural Killer Cell-mediated Cytotoxicity Assay
    Lonza White Paper
  • Validation of Cytokines for the Chemically Defined Manufacturing of Human CD34 Positive Hematopoietic Precursor Cells
    Lonza Poster
  • A Novel, Chemically Defined, Serum-Free Cell Culture Medium for Expansion of Transfected T Cells
    In this study, we present data generated with TheraPEAK® T-VIVO®, a novel, chemically defined, non-animal origin cell culture medium utilized to grow T cells in the absence of serum, before and after transfection with the Nucleofector® Technology.
  • A 3D Bioprinted Model to Study Osteogenic Differentiation of Primary Mesenchymal Stem Cells
    Learn from this white paper how a 3D bioprinted model using hMSCs can be used for evaluation of bioink compatibility and bioprinting processes.
  • Synthego-Lonza Genome Editing of Resting T cells
    Case Study on Genome Editing of Resting T cells
  • Webinar - Hepatocytes in the Drug Development Pipeline
    Overview of how primary hepatocytes are used in drug development
  • TheraPEAK® T-VIVO® Cell Culture Medium – Overview
    View or download this document for a comprehensive overview and learn how the chemically defined TheraPEAK® T-VIVO® Medium enhances T-cell culture and accelerates therapy development.
  • Automated Cell Signaling Assays Using Primary HUVECs
    Lonza's Primary HUVECs are an excellent cell type to measure the effects of pharmacologically-important compounds on vial signaling pathways, and they provide increased data relevancy compared to cell lines.
  • First siRNA Library Screening in Hard-to-Transfect HUVEC and Jurkat Cells
    High throughput transfection of siRNA libraries has become a valuable tool in target identifi cation and validation. However, such screenings have so far been constrained to mostly easy-totransfect adherent cell lines. Lonza’s 96-well Shuttle® System, based on the well-established Amaxa® Nucleofector® Technology, extends these approaches to primary and diffi cult-to-transfect cells.
  • Transfection of Primary Human Hepatocytes
    Efficient Transfection and Sustained Long Term Functionality
  • Poster: eCHO® Basal Medium and Feed for CHO cells
    This poster demonstrates the performance of Lonza’s easy, economical, chemically defined, animal origin-free, simple one part eCHO® Basal Medium and one part eCHO® Feed for CHO cells to produce recombinant proteins.
  • Efficient Transfection of Cancer Cell Lines Using the 4D-Nucleofector™ System
    Product data sheet showing efficient tranfection of cancer cell lines
  • SourceBook Section II - Preparation of Agarose Gels
    1. Agarose Selection Guide 2. Agarose and Compatible Techniques 3. Agarose Types 4. Agarose Analytical Specifications 5. Suggested Agarose Concentrations & Dye Migration Information 6. Buffers for Electrophoresis 7. Dissolving Agarose 8. Casting Agarose Gels
  • PowerCHO® Protein Expression Media brochure
    Overview of the PoweCHO medium (new PowerCHO Advanced not included)
  • Instructions - PowerCHO™ Medium
    How to use the different PowerCHO™ Media
  • Instruction PowerCHO powder kits
    Instructions for use of PowerCHO Powder kits
  • Instruction ProFreeze-CDM NAO Freezing Medium (2X)
    Short instruction how to use Freezing medium without Serum
  • Instruction UltraMDCK™ Serum-free Medium
    Instruction how to use UtraMDCK™ Medium (12-749)
  • BE02-056Q CHO Xtreme™ Feed CD - Instructions
    BE02-056Q
  • GSv9™ Media and Feeds
    Let’s maximize your protein expression together. Media and feeds designed for Lonza’s GS System®
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