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Cell Assays
DNA Assays
Maintenance and Troubleshooting
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Click a question below to see the answer:
How many cell samples can be analyzed on one cell chip?
I understand the samples are analyzed one after the other. How can I be sure that there is no cross-contamination from one sample to the next?
Can I re-use a cell chip after a run?
How long does it take to prepare and run a cell chip?
Can I store stained cells overnight before the chip run?
What cell concentrations are needed to run a sample on the cell chip?
How many cells are needed per sample?
What is on-chip staining?
What are the channel dimensions and what cell size works?
Can I analyze prokaryotic or yeast cells on the bioanalyzer?
What is the difference between the cell assay checkout kit and the cell fluorescence kit?
How can I decide if a dye is compatible with the bioanalyzer optics?
Currently I use FITC-labeled antibodies. Can I use them on the bioanalyzer?
Is there a color compensation necessary with the 2100 bioanalyzer? Or is one color bleeding to the next color?
Can the bioanalyzer detect unstained cells?
Are blood cells an appropriate sample for the bioanalyzer?
Are shear stresses a problem in the micro-fluidic channels?
Are cell clumps or agglomerates a problem for the cell chip?
Do I need to make any calibration before starting cell analysis?
Is it complicated to switch the bioanalyzer from molecular assays to cell assays and back again?
What is the difference between the generic assay and the other assays in the software?