Q:

Do you have any instructions available for using a hemocytometer for cell counting?

A:

Yes. Our technical guideline "Cell Counting and Determination of Viability via Hemocytometer" can be found as associated pdf file in the link below.

Categories:
Primary Cells and Media
Transfection
Laboratory Instrumentation
Research Areas:
Basic Research

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.