Introducing New DA-Cell™ Technology for Improved Flow Cytometry
Cell processing technology enabling superior staining and retention of suspension cells using centrifuge-less washing.
The DA-Cell technology provides an advantage to scientists in retaining higher cell numbers without jeopardizing data integrity. Eliminating the usage of the centrifuge has tremendously improved workflows and time management prior to FACs analysis. In the conventional flow cytometry protocol which utilizes the centrifugation method, immune cells undergo numerous washes that generate significant stress to cells. This in turn increases the alteration of biomarker pathways as well as cell loss.
With the laminar flow wash technique of the DA-Cell system, cells undergo a gentle wash without added stress, allowing a higher retention of cells for acquisition and cell sorting. In addition, cell surface markers are not modified and unbound antibodies are washed off efficiently, producing cleaner and better segregated data. For high throughput flow cytometry labs, they will be able to achieve consistency by reducing variation from manual handling.
The DA-Cell has been successfully demonstrated on various applications including immunophenotyping and CyTOF. Some of the lymphocytes and cell surface markers tested, with improved cell retention and data are as follows:
• Antigen presenting cells (CD40) such as B-cells (CD34, CD45) and dendritic cells
• T-cells – Cytotoxic T cells, Helper T cells (CD3, CD4, CD8)
• Cell lines: HEK293T, Yeast cerevisea, CHO, U937, Ramos, Molt4, THP-1, MOM13
• Primary Mouse Tumor Cells
• Mouse Primary Splenocytes
• Colorectal Tumor cells
• Circulating Tumor cells
• Isolated Nucleii
• Thymic Epithelial cells from Mouse
• Mouse Brain cells
• Nucleated red blood cells from maternal blood / cord blood
See How DA-Cell Works:
DA-Cell enables >95% cell retention and results in superior data over microtiter plates/centrifugation
Direct HTS acquisition by flow cytometer on DA-Cell
Equivalent acquisition efficiency and stability as U-bottom plate
Efficient cell mixing even with low cell concentration
Mouse splenocytes (250,000 cells) seeded per well of DA-Cell plate with accessory grid or U-bottom plate, and volume topped up, brought to 150uL with FACS buffer. Cells were acquired by HTS on BD Celesta flow analyzer, and gated for lymphocytes by FSC-SSC scattering. (Acquisition speed: 1.0uL/s. Mixing volume: 100uL. Mixing speed: 100uL/s. No. of mixes: 5
Placement of grid increases volume per well for efficient cell mixing by HTS probe
Washing Whole Blood Without a Centrifuge – Human and Mouse
Lysing and washing red blood cells using traditional microtiter plates or tubes may result in significant cell loss and damage.
There is now a better way to lyse RBCs while achieving clean antibody staining and lysis as good as or better than traditional methods. The new DA-Cell™ system offers centrifuge-less blood lysis and leukocyte washing on a single platform, with efficient RBC and debris removal. Whole blood lysis performed by DA-Cell has similar leukocyte retention compared to lysis with centrifugation, whether enumerated by CD45 staining or FSC-SSC scattering
The scatter plot above is derived from human whole blood lysed and stained on DA-Cell™ vs. Microtiter plate vs. FACS tube (L to R).
The scatter plot above is derived from mouse blood with TER119 vs. CD45 using DA-Cell™ vs. Microtiter plate vs. FACS tube (L to R).
Note the clean staining using DA-Cell.
DA-Cell lets you achieve:
- Consistency by reducing variation from manual handling
- Time savings by completing cell washing in 3 minutes
- Reduced cell stress due to no centrifugation
- Easy integration into your lab automation