amaxa - Part of the Lonza Group
 
 
You are not logged in. Log in

FAQ Search Results

195 FAQ articles available.

previous  1  2  3  4  5  6  7  8  9 [10]  11  12  13  14  15  16  17  18  19  20  next

  1. I followed the protocol, but I observed low viability with my hepatocytes. What should I do?

  2. Is it more difficult to detect DsRed by FACS than GFP?

  3. What kind of suspension CHO cells did you use for protein production?

  4. Can I use the pmaxGFP® control plasmid with insect cells such as S2 cells or SF9 cells?

  5. Do you have any information regarding differentiation of mouse ES cells after nucleofection® with large plasmids?

  6. Does the Mouse T cell protocol work for stimulated mouse T cells?

  7. Is it possible to transfect proteins using the Nucleofector® technology?

  8. Can I apply more than one program (transfection condition) per plate with the 96-well Shuttle® System?

  9. What cell number do I need per well when using the 96-well Shuttle®?

  10. What is the amount of DNA needed per well when using the 96-well Shuttle®?

previous  1  2  3  4  5  6  7  8  9 [10]  11  12  13  14  15  16  17  18  19  20  next


Go back to the > FAQ search or view the > complete FAQ list.