OC-400 RUO™

Catalogue No.

OC-400 RUO™
  • Description
  • Graph Details

Supplier

MaxCyte

|

Catalogue No.

OC-400 RUO™

OC-400 RUO™

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.

OC-400 RUO™

  • Mid-scale applications and scale-up optimization
  • For quick single sample transfection
  • Specifically designed for efficient cell loading and recovery

Configuration: Single well, 400 µL maximum volume
Cell Range: 1×106 – 8×107
Volume Range: 200 – 400 µL
Application: Research Use Only
Catalog: SOC-4

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.

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.

OC-400 RUO™

  • Mid-scale applications and scale-up optimization
  • For quick single sample transfection
  • Specifically designed for efficient cell loading and recovery

Configuration: Single well, 400 µL maximum volume
Cell Range: 1×106 – 8×107
Volume Range: 200 – 400 µL
Application: Research Use Only
Catalog: SOC-4

Compatible with ATx™ and STx™

Graph Details icon

OC-400-v-CL-1@2x

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 expression on a flow cytometer after 48 hours.

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