rh at mblab.gla.ac.uk
Tue Jan 16 13:02:08 EST 2001
In article <3A640393.8B8B6B42 at unav.es>, joses at meseta.unav.es (Juan
> Hi !
> I would like to know why you have to add 5% of CO2 in cell cultures. It
> is used in all protocols I have read.
It keeps the pH correct in Eagles Bicarbonate buffered systems for eg.
For a look at different culture media constituents get a copy of the Life
technologies cell culture catalogue.
You don't always have to use CO2, EG endothelial cultures that I grow in
HEPES buffered media.
As a wee funny one:- something happened on Sun/Mon to me.
I normally grow my stock Macrophage in RPMI HEPES buffeed with no C02. I
GOT SOME NEW ONES IN FROM A COLLEAGUE SINCE HE TOOK ALL MINE. :-) ahh
I asked him if he gassed them with CO2 and he said "no" ( he uses a
different media). So I subbed as normal while commenting to my girlfriend
(a physisist), that, in general RED coloured media (phenol red indicator)
are CO2/Bicarb buffered. When I came in on monday and found that half of
them had detached, I asked my colleague about the CO2.
He said " I don't gas them personally I have a CO2 incubator".
And the moral is "it stops your cells from dying" :-)))))))
Bob; Chilly Scotland
Robert Hartley, Centre for Cell Engineering,University of Glasgow,
Glasgow G12 8QQ Tel:++44(0)141 330 4756
Fax:++44 (0)141 330 3730 mailto:rh at mblab.gla.ac.uk
Web : http://www.gla.ac.uk/Inter/CellEngineering
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