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Posted by: zcshen Jul 27 2002, 11:09 AM

Sir,
I am trying to separate and culture human monocytes.But I still could find any macrophages/monocytes in the flask after 23 days culturing.
My procedure is :
1 Use Ficoll paque to separate lymphocytes and monocytes from blood.
2 by incubating with RPMI 1640 for 4 hours, remove lymphocytes from the suspension, those cells attached on flask wall were considered monocytes.
3 culture the monocytes in 37C 5% CO2 condition, changed medium 3-4 days.
For RPMI 1640 type, I used the formula with L-glutamine and added 2 g sodium carbonate  in 1 Liter.

I am not sure if the monocytes can split or not?
How many days take them to become as big as 50 um?
What's the problem with the procedure?

I  highly appreciate your help.

zcshen73@yahoo.com
zancong  shen
Chem Engineering
University of California-santa barbara
CA 93106