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DonorPlexTM Pooled Donor Human Hepatocytes, 10 Donor, Female
Catalog #: HUCS10PF
Pooled 10-donor female only human hepatocytes that are characterized for multiple CYP450, UGT, SULT, and transporter activities. Ideal for drug metabolite identification, characterization, and turnover kinetics.
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DonorPlexTM Pooled Donor Human Hepatocytes, 20 Donor, Female
Catalog #: HUCS20PF
Pooled 20-donor, female only human hepatocytes that are characterized for multiple CYP450, UGT, SULT, and transporter activities. Ideal for drug metabolite identification, characterization, and turnover kinetics.
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DonorPlexTM Pooled Donor Human Hepatocytes, 10 Donor, Male
Catalog #: HUCS10PM
Pooled 10-donor, male human hepatocytes that are characterized for multiple CYP450, UGT, SULT, and transporter activities. Ideal for drug metabolite identification, characterization, and turnover kinetics.
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DonorPlexTM Pooled Donor Human Hepatocytes, 20 Donor, Male
Catalog #: HUCS20PM
Pooled 20-donor male only human hepatocytes that are characterized for multiple CYP450, UGT, SULT, and transporter activities. Ideal for drug metabolite identification, characterization, and turnover kinetics.
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DonorPlex™ Pooled Donor Human Hepatocytes, 50 Donor, Mixed Gender
Catalog #: HUCS50P
Pooled 50-donor, mixed-gender human hepatocytes that are characterized for multiple CYP450, UGT, SULT, and transporter activities. Ideal for drug metabolite identification, characterization, and turnover kinetics.
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Human Bone Marrow Stromal Cells, 5 Million
Catalog #: 2M-302
Cryopreserved ampule of Human Bone Marrow Stromal Cells containing ≥5 million cells
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Diabetic Type I & Type II Adipose Derived Stem Cells (ADSC)
Catalog #: PT-5007
Human ADSC, cryo amp, ≥1 million cells, Diabetes Type I
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Diabetic Type I & Type II Adipose Derived Stem Cells (ADSC)
Catalog #: PT-5008
Human ADSC, cryo amp, ≥1 million cells, Diabetes Type II
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Primary Cell Optimization 384-well Nucleofector® Kit
Catalog #: V5SP-9001
For high-throughput optimization of transfection conditions for primary cell types lacking an Optimized Protocol for the 384-well HT Nucleofector® System
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Primary Cell Optimization 4D-Nucleofector® X Kit
Catalog #: V4XP-9096
For rapid determination of Nucleofection conditions for primary cell types lacking an Optimized Protocol for the 4D-Nucleofector® X Unit.
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Primary Liver Endothelial CellsImportance of passage number in measuring the uptake of large molecules
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Instructions - Human Liver Endothelial Cells (HLEC)Instructions for proper use and culture of Human Liver Endothelial Cells
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The Importance of Cell-subtype Selection in Creation of a 3D Liver Fibrosis ModelData sheet detailing 3D liver fibrosis model in collaboration with Visikol
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Engineering Culture Platforms to Mimic Liver DiseasesLearn from Dr. Salman Khetani, University of Illinois at Chicago, how multiple liver cell-types including hepatocytes, Kupffer, stellate, and endothelial cells can be engineered together to model human liver disease phenotypes in culture. -
Endothelial Cells Concentration Guide
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NPCs Hepatic Non-Parenchymal CellsThese additional liver cell types provide a complete building set supporting complex cell culture modeling. Applications include developing more physiologically relevant in vitro models for complex liver diseases and toxicity testing of new drugs and chemicals.
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Metabolism_Brochure_CoBrand_FormThis is a co-marketing form for distributors. There is a restricted space on the cover next to the Lonza logo and on the back below the market bar. Art for placement MUST be a PDF. In addition there is space on the back cover for a web address at the top and contact and disclaimers. Please look for the instruction PDF in the literature DB Article number CD-FO006Inst
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Tech/Instruction Sheet - Cond. Immo. HMVEC-BrTechnical information and instructions for culturing CloneticsTM Conditionally Immortalized Human Brain Microvascular Endothelial Cell
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TechSheet - Aortic Endothelial Cell SystemsTechnical information sheet for Clonetics™ Aortic Endothelial Cells
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A Novel In Vitro Liver Cell Culture Flow System Allowing Long-Term Metabolism and Hepatotoxicity Studies]Manuscript published in Applied In Vitro Toxicology journal describes improvement of CYP450 phenotype of primary cryopreserved hepatocytes using Quasi Vivo® System
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