Culture system containing REBM® Basal Medium (CC-3191) and REGM® SingleQuots® supplements (CC-4127) required for growth of Renal Epithelial Cells.
Cryopreserved ampule of Mouse Brain CD1 Hippocampus Neurons containing ≥ 1,000,000 cells
Human CD19+ B cells isolated from peripheral blood using positive immunomagnetic selection, cryopreserved, ≥10 million cells
Human CD3+ T cells, isolated from peripheral blood using negative immunomagnetic selection, ≥ 25 million cells, cryopreserved
Cryopreserved ampule of Human Peripheral Blood CD14+ Monocytes, negative selection, containing ≥10 million cells
Cryopreserved ampule of negatively selected Human Peripheral Blood CD14+ Monocytes, containing ≥ 50 million cells
Cryopreserved ampule of Human CD34+ Progenitor Cells from Mobilized Peripheral Blood using positive immunomagnetic selection containing 10 million cells
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Instructions - UltraCHO™ MediumHow to use ProCHO medium
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Instructions – ProCHO Liquid mediaInstructions for use of ProCHO Media
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Instructions ProCHO powder kitsInstructions for use of ProCHO Powder kits
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ProCHO® Protein Expression Media
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WinKQCL 5 Software - EnglishWe Analyze Endotoxin Data Every Day Version 5 Software Features Announcement of discontinued support for Windows SQL Server® 2000 and XP Operating System English Version
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WinKQCL™ 5 Endotoxin Detection SoftwareLearn how to use the advanced features in Lonza's WinKQCL™ Endotoxin Detection Software to save time, reduce costs and ensure compliance to 21 CFR Part 11 and Annex 11. -
4D-Nucleofector® Protocol for MRC-5Optimized 384-well Nucleofector® and 4D-Nucleofector® Protocol for MRC-5
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MRC-5 Transfection Protocol - 4D-Nucleofector™ DeviceInstructions of use for transfection of MRC-5 with the SE Cell Line 4D-Nucleofector™ X Kit
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WinKQCL™ 5 Software – Discover the Fast Track to Endotoxin AnalysisWebinar about the WinKQCL™ 5 Endotoxin Detection and Analysis Software and how it can help you to analyze, report and trend your data. -
SourceBook Section III - Loading and Running DNA in Agarose Gels1. DNA Loading 2. Loading Buffers 3. Optimal Voltage and Electrophoretic Times 4. Fast Running Protocols for High Resolution in MetaPhor® Agarose Gels 5. References