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  1. Can amaxa’s antibiotics be used in clinical trials?

  2. What filters do you recommend for the visualization of the fluorescent proteins expressed by your pmaxFP® vectors?

  3. Does the cap need to be on the cuvette during the nucleofection® process?

  4. Are your Nucleofector solutions checked for RNase activity during your QC process?

  5. What is the difference between pro-B cells and pre-B cells?

  6. What kind of buffer do you recommend for resuspending my siRNA?

  7. When should one use Plasmocin™ versus Normocin™?

  8. What stock concentration of Propidium Iodide does amaxa use for FACS analysis?

  9. Can your Nucleofector technology be used for diagnostic purposes or for testing or treatment in Humans?

  10. In your optimized protocols for MDA-MB-231 and MDA-MB-468, you say to culture the cells without CO2. Why?

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