For efficient transfection of specific primary cells, e.g. mouse B-cells or mouse immature DCs, in the 4D-Nucleofector® X Unit (20 µL format).
For adherent electroporation of primary cells, e.g. neuronal or endothelial cells, when working with the 4D-Nucleofector® Y Unit.
For efficient transfection of specific primary cells, e.g. HUVEC, in the 4D-Nucleofector® X Unit (20 µL format).
For high-throughput transfection of cell lines, e.g.Ba/F3, Raji or THP-1, when working with the 384-well HT Nucleofector® System.
Cryopreserved ampule of Human Dental Pulp Stem Cells containing ≥1 million cells
Complete cell culture kit containing a cryopreserved ampule of Bronchial Epithelial Cells (CC-2540) and BEGM® Growth Media BulletKit® (CC-3170) for culture of Bronchial Epithelial Cells.
For efficient transfection of specific primary cells, e.g. human ADSCs or MSCs, in the 4D-Nucleofector® X Unit (100 µL format).
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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