CL-1.1™ RUO

Catalogue No.

  • Description
  • Graph Details

Supplier

MaxCyte

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Catalogue No.

Processing Assemblies

Mid-scale RUO Processing Assemblies
Static electroporation processing assemblies for research applications in mid-volume scales.

Mid-scale RUO Processing Assemblies

Static electroporation processing assemblies for research applications in mid-volume scales.

Research Use Only (RUO) Processing Assemblies enable the discovery and development of applications at mid-scale. These static electroporation consumables are made from high-grade, inert materials to protect precious cells with additional design features for easy sample loading and recovery.

CL-1.1™ RUO

  • Closed chamber with luer locking syringe port
  • Mid-range production scale
  • Made from high grade, inert materials to protect precious cells

Configuration: Closed chamber, 3.5 mL maximum volume
Cell Range: 5×10⁶ – 7×10⁸
Volume Range: 1 – 3.5 mL
Application: Research Use Only
Catalog: SCL-1
Compatible with: ATx™ and STx™

  • Description
  • Graph Details
Description icon

Mid-scale RUO Processing Assemblies
Static electroporation processing assemblies for research applications in mid-volume scales.

Mid-scale RUO Processing Assemblies

Static electroporation processing assemblies for research applications in mid-volume scales.

Research Use Only (RUO) Processing Assemblies enable the discovery and development of applications at mid-scale. These static electroporation consumables are made from high-grade, inert materials to protect precious cells with additional design features for easy sample loading and recovery.

CL-1.1™ RUO

  • Closed chamber with luer locking syringe port
  • Mid-range production scale
  • Made from high grade, inert materials to protect precious cells

Configuration: Closed chamber, 3.5 mL maximum volume
Cell Range: 5×10⁶ – 7×10⁸
Volume Range: 1 – 3.5 mL
Application: Research Use Only
Catalog: SCL-1
Compatible with: ATx™ and STx™

Graph Details icon

Graph Details: To make a master mix, HEK 293 cells were suspended in MaxCyte Electroporation Buffer at a density of 1×108 cells/mL with pGFP at 200 µg/mL. 400 µL of the master mix was loaded into the OC-400, 1 mL was loaded into one CL-1.1 and 3.5 mL was loaded into a second CL-1.1. Transfection was performed using the MaxCyte HEK electroporation protocol for all 3 PAs. Cells were plated at 3 different densities post-transfection and were analyzed for fluorescence after 48 hours.

 

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