Q:

Does phenol red in the cell culture medium interfere with the ToxiLight™ Non-Destructive Cytotoxicity BioAssay?

A:

The assay has been developed in the presence of phenol red so all the example data has been conducted in complete media. Phenol red does quench the light signal so if you compared assays in phenol red free media they would have higher RLUs. The ToxiLight™ BioAssay generates so much light that the slight quenching by phenol red has never been a problem.

Categories:
Bioassay

You may also want to know:

What selection markers can I use for the generation of stable cell lines?
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?
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 much DNA should I use in my Nucleofection® Reaction to obtain stable clones?
How long does it take to obtain stable transfectants?
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 ?
Why is the Nucleofector®Technology ideal for primary cells and difficult-to-transfect cell lines?
Following Nucleofection®, I cannot obtain stable clones from single cells. What could be the reason?
See More

Privacy | Legal | About Lonza

© Lonza. All rights reserved.