Dyes for cell tracking experiments... -Reply

Nicholas King (nickk@med.su.oz.au)
Wed, 24 Jul 1996 11:02:47 +1000

Zip,

Your best bet in my view is the dye carboxyfluorescein succinimidyl ester;
Do a line search for Parish, C. He has used it best (and I believe first).
It has all the attributes you need, and excites at 488nm. You can even
enumerate proliferation generations with it.

Regards,
Nick

We intend to perform an experiment which will involve the labelling of
isolated mouse tumour cells with a fluorescent dye, prior to introducing
these cells into a mixed population. The idea is to be able to detect these
original cells in the mixture by flow, after a period of time lasting around
two hours. So, the question is this: which dye would any of you esteemed flow
gurus recommend for this, which will:-

Readily be taken up by viable cells.
Not be removed by washing immediately afterwards.
Persist for at least two hours, without serious loss of fluorescence.

Potential excitation wavelength for the dye to be used is not a
problem, as the analysis will be performed using a FACStar+ with a choice of
488nm., UV & dye laser excitation available.


Home Page Table of Contents Sponsors Web Sites
CD ROM Vol 2 was produced by staff at the Purdue University Cytometry Laboratories and distributed free of charge as an educational service to the cytometry community. If you have any comments please direct them to Dr. J. Paul Robinson, Professor & Director, PUCL, Purdue University, West Lafayette, IN 47907. Phone:(317) 494-0757; FAX (317) 494-0517; Web http://www.cyto.purdue.edu EMAIL robinson@flowcyt.cyto.purdue.edu