R-50×3™

Catalogue No.

R-50×3™
  • Description
  • Graph Details

Supplier

MaxCyte

|

Catalogue No.

R-50×3™

R-50×3™

Small-scale RUO Processing Assemblies
Static electroporation processing assemblies for research applications in small volume scales with both single-well and multi-well options.

Research Use Only (RUO) Processing assemblies aid the discovery and development of applications at small scales. 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.

R-50×3™

  • Research & development applications
  • Efficient 3 sample processing per transfection
  • Easy cell recovery with V-shaped well design

Configuration: 3-well, 55 µL maximum volume per well
Cell Range: 2.25×105 – 1.1×107 per well
Volume Range: 45 – 55 µL per well
Application: Research Use Only
Catalog: ER050U3-10

Compatible with ATx™ and STx™

  • Description
  • Graph Details
Description icon

Small-scale RUO Processing Assemblies
Static electroporation processing assemblies for research applications in small volume scales with both single-well and multi-well options.

Research Use Only (RUO) Processing assemblies aid the discovery and development of applications at small scales. 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.

R-50×3™

  • Research & development applications
  • Efficient 3 sample processing per transfection
  • Easy cell recovery with V-shaped well design

Configuration: 3-well, 55 µL maximum volume per well
Cell Range: 2.25×105 – 1.1×107 per well
Volume Range: 45 – 55 µL per well
Application: Research Use Only
Catalog: ER050U3-10

Compatible with ATx™ and STx™

Graph Details icon

GFP_Wash-U-Beta-Data@2x

Graph Details: Primary human natural killer (NK) cells were collected from 4 individual donors and activated overnight in 1 ng/mL IL-15. The following day, 3 – 4 x 106 NK cells along with 5 μg mRNA GFP and 45 μL MaxCyte Electroporation Buffer was loaded into each well of the R-50×3 processing assembly and the OC-100 was used as the device control. Cells were electroporated on the MaxCyte GTx™ instrument, then collected and cultured in 1 ng/mL IL-15 media for 24 hours then assessed by flow cytometry. Graphs show the average results and standard error of cells taken from 4 individual donors electroporated with 5 processing assemblies, 2 used for the same donor, with each well of the R-50×3 analyzed individually. The negative control is the average of 4 samples. Experimental data courtesy of Dr. Todd Fehniger’s Laboratory, Washington University in St Louis, Department of Medicine, Division of Oncology with special appreciation to Pamela Wong.

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