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  1. Why is the Nucleofector® technology ideal for protein production from stable clones ?

  2. How many cortical neurons can I expect from a single pup?

  3. Does the 96-well Shuttle® recognize if the cuvette plate is in backwards?

  4. Do any of the three instruments used in the 96-well Shuttle® system "go to sleep" or power off automatically?

  5. What is the molecular weight of your control pmaxGFP® plasmid?

  6. What is the molecular weight of the GFP protein expressed by your control pmaxGFP® plasmid?

  7. I want to stimulate human primary T-cells with anti-CD3 and anti-CD28. Do you have a detailed protocol for this?

  8. Can I open the 96-well Shuttle® software files by double-clicking on the file name?

  9. Do you have data about the in vivo implantation of hepatocytes transfected by nucleofection®? For how long could protein expression be detected?

  10. Are rat and mouse hepatocytes transfected by nucleofection® still functional?

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