Q:

How can I remove the cells from the 100 uL Nucleocuvette® Vessel after Nucleofection®? Is there any alternative?

A:

We recommend using the plastic single use pipettes provided in the kits. These pipettes prevent any damage to the cells and ensure a good cell recovery.

Categories:
Transfection

You may also want to know:

Generation of a stable cell line: A positive control plasmid works, but I cannot obtain stable clones with my construct of interest. What could be the reason?
How long does it take to obtain stable transfectants?
What selection markers can I use for the generation of stable cell lines?
Is your pmaxGFP control vector supplied with the Nucleofector® Kits suitable for stable expression?
How many stable clones will I get from one transfection?
Why is the Nucleofector® Technology ideal for protein production from stable clones ?
In stable cell line generation, I have a very high transfection efficiency, but most of my cells die during selection. Is this to be expected?
Following Nucleofection®, I cannot obtain stable clones from single cells. What could be the reason?
How long is the MycoAlert® Mycoplasma Detection Assay signal stable?
What antibiotic concentration should I use for selecting stable transfectants?
See More

Privacy | Legal | About Lonza

© Lonza. All rights reserved.