LeviCell

• What is the split line?
• Does the Levitation Agent contain any human or animal ingredients?
• What kind of gene expression changes have you seen after running through LeviCell?
• Do I need any antibodies?
• Which fluorescent reagents can I use with LeviCell 1.0 and LeviCell EOS?
• Is DRAQ7 compatible with the LeviCell?
• How many cells can I load at once?
• How does the system enrich the top or bottom fraction?
• What is the output volume of the run?
• How long does a run take?
• What happens if my cells are clumping?
• How can I optimize separation for my application?
• What is the difference between cell size and cell density?
• Can you distinguish between different cell types?
• Why is the equilibration time longer for smaller particles than it is for large?
• What is the largest size particle/cell that can be run on the system?
• Can I use samples which are more viscous than water, such as cell culture media?
• What types of samples can I start with?
• What types of cells have you tested?
• Do I need beads, stains, or any labels?
• What determines levitation height?
• Do we have to remove or wash out Levitation Agent for downstream studies?
• What media formulations are compatible with the LeviCell?
• Are the cells damaged or affected in any way?
• How does the Levitation Agent interact with cells?
• What is the Levitation agent?
• What excitation and emission do the green and red Channels have?
• Error on start-up, Tecan pumps not detected
• Using Resume Workflow
• What stresses do the cells experience during levitation
• Why are there viable cells in the bottom fraction?
• Sample remains in the inlet well