4D-NucleofectorTM LV Unit
For closed, scalable large-scale transfection of up to 1x109 cells
What You May Also Need
Product Overview
Large-Scale Transfection Using the 4D-NucleofectorTM LV Unit - Experience the new functional unit for the 4D-NucleofectorTM System which expands our proven system to larger-scale transfection. The LV Unit allows for closed, scalable transfection of larger cell numbers in the range of 1x107 to 1x109 cells. Transfection protocols can be established in smaller scale using the X Unit and subsequently transferred to the LV Unit without the need for re-optimization. Transferability has been tested for various cell types, including human T cells, CHO-S, HEK293-S, or K-562.
There are cell type-specific Optimized Protocols or recommendations available in our knowledge database. In these Optimized Protocols the best Nucleofection conditions are indicated. In addition, we share our experience and knowledge for treatment of individual cell types.
Technical Specifications
Dimensions: (w x h x d): 24.5×20.7×28 cm / 9.7×4.1×11.0
Weight: 5.7 kg (12.5 lb)
Power: 100 - 240 VAC
Frequency: 50 - 60 Hz
Consumption: 0 VA (power off) / 20 VA (idle) / 140 VA (busy - during transfection)
Fuse: T 2.5A, L250V
Operating temperature: +15°C up to +40°C (59°F - 104°F)
Environnement non condensing Voltage limitation: 1500 V
Current limitation: 100 A
Quality statement: We are applying ISO9001:2015 standards for the design, manufacturing and testing of NucleofectorTM Devices, Solutions and Consumables since 2004.
Note: For use of the 4D-NucleofectorTM LV Unit you need the first generation 4D-NucleofectorTM Core Unit as controlling unit. For receiving a quote, please use “Request a quote” button above.
Benefits
- Closed system: Sterile Nucleofection of up to 109 cells
- Real scalability: Optimization in small scale
- Established protocols: Benefit from 700+ optimized cell types
- Simple handling: Minimal training needs
- 4D-NucleofectorTM LogWare: Optional operation via 21CFR part11 compliant software
Applications
- Ex-vivo modification of human primary cells for cell therapy applications (e.g. genome editing, generation of CAR-T cells)
- Transient production of potential therapeutic proteins or antibodies for construct screening
- Generation of large numbers of transiently modified primary cells for cell-based assays
Content & Storage
Content
1 Unit
Instructions
Safety Data Sheets (SDS)
Certificate of Analysis (CoA)
Please enter Lot Number, including all zeros, located on the product label and please take into account that it is case sensitive.Brochures, White Papers etc.
Lonza GS XceedTM Cells transfected in small or larger scale show comparable IgG4 titers
For a human IgG4 antibody, similar titers of about 100 µg/mL were achieved in small scale (100 µl) and large scale transfections (1 ml fixed cartridge or 10 mL in flow through LV cartridge) in a 6-day batch culture without any feeds. IgG titers were increased by factor 2.5 when using higher seeding densities (not shown here). Switching to a 14-day fed-batch culture led to titers > 1 mg/mL (not shown here).
Transfection of GFP mRNA into PBMCs
Fresh PBMCs (1x10⁸/mL) were transfected with GFP mRNA (20 µg/mL) using different NucleofectionTM Vessels. For the fixed volume vessels (100 µL NucleocuvetteTM Vessel and 1 mL NucleocuvetteTM Cartridge), cells and mRNA for each sample were mixed separately, pipetted into the vessel and pulsed immediately. For the flow-through LV NucleocuvetteTM Cartridge two feeding reservoirs were used to keep cells and mRNA separate as long as possible. Data are based on duplicates (experiment 1) or unicates (experiment 2).
