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214 FAQ articles available.

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  1. When I transfected my cells, the message "weak" appeared on the display of the Nucleofector®. What does that mean and what is the reason for this error?

  2. Where can I find what the error codes on the Nucleofector® or 96-well Shuttle® mean?

  3. What kind of luciferase assay did amaxa use in the application note "Important Vector Factors for Gene Expression"?

  4. How can I determine the concentration of my expressed protein?

  5. According to which standard is the Nucleofector® device certified?

  6. The Optimized Protocol I am using recommends a certain plating density. Can I plate my cells at a lower density?

  7. Is it typical for the fluorescence observed from my tagged protein to appear less than the empty fluorescent vector?

  8. How critical is the time point for analysis post transfection?

  9. Do we sell the solution (or any other component of the kit) separately?

  10. Where can I find pricing on the website?

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