WiCell Undifferentiated Status Assessment by Flow Cytometry Assay
WHAT IS THE UNDIFFERENTIATED STATUS?
Regular assessment of stem cell cultures is essential to monitor changes in morphology, karyotype, and differentiation potential. Over time, as cells adapt to their culture conditions, the composition of the population can shift due to selective pressures on the cells. This makes routine monitoring of key quality attributes essential for maintaining culture purity, ensuring research reproducibility, meeting regulatory standards, and validating outcomes in both research and therapeutic contexts.
With 25 years of stem cell expertise, WiCell can reliably execute characterization assays to confirm the undifferentiated status of your cell lines and ensure the integrity of your research.
WICELL’S UNDIFFERENTIATED STATUS ASSESSMENT BY FLOW CYTOMETRY ASSAY
Data analysis is performed using FCS Express™ from De Novo Software. First, non-viable cells are excluded using the LIVE/DEAD™ Green Dead Cell Stain Kit (Invitrogen™). Data files undergo a gating process that first filters for cells (excluding debris), followed by singlets, and then live cells. Compensation matrices are computationally generated from single-color controls and applied to all sample data files. All data for samples and compensation controls are acquired on the same day on the same instrument to ensure consistency.
Subsequent gating for Oct4 and Nanog expression is performed in two ways to determine (1) the percent dual expression, and (2) the percent dual high expression of the sample cell line:
Dual Expression
The percentage of cells expressing both Oct4 and Nanog is determined. Dual expression is gated using Fluorescence Minus One (FMO) controls, where either Oct4 or Nanog antibodies are omitted.
Figure 1. Dual Oct4 and Nanog Expression. Quadrant gates established from the FMO stain are utilized to analyze the dual expression of Oct4 and Nanog. This cell line exhibits 97% positive dual expression of both markers.
Dual High Expression
The percentage of dual high expression of Oct4 and Nanog is determined. Dual high expression is gated using a contour plot to define the population of cells with high levels of both Oct4 and Nanog expression.
Figure 2. Dual High Oct4 and Nanog Expression. The gate drawn on the contour plot identifies the boundaries where the dominant double-positive population begins to noticeably separate at the leftmost and lowest points. This cell line exhibits 88% positive high dual expression of both markers.
SUBMITTING SAMPLES
SAFEGUARD YOUR STEMCELL RESEARCH
Additionally, WiCell provides flow cytometry testing services to assess pluripotency following in vitro trilineage differentiation to ensure thorough characterization of your stem cell lines.
Contact us for inquiries about assay customization, live culture sample submission, or any other questions.
REFERENCES
- Ludwig TE, Andrews PW, Barbaric I, et al. ISSCR standards for the use of human stem cells in basic research. Stem Cell Reports. 2023;18(9):1744-1752. doi:10.1016/j.stemcr.2023.08.003