Improved soft-agar colony assay in a fluid processing apparatus |
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Authors: | Allan D. Forsman Angela R. Herpich Stephen K. Chapes |
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Affiliation: | (1) Present address: Department of Aerospace Engineering Sciences, University of Colorado, 80309 Boulder, Colorado;(2) Division of Biology, Kansas State University, 19 Ackert Hall, 66506-4901 Manhattan, Kansas |
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Abstract: | Summary The standard method for quantitating bone marrow precursor cells has been to count the number of colony-forming units that
form in semisolid (0.3%) agar. Recently we adapted this assay for use in hardware, the Fluid Processing Apparatus, that is
flown in standard payload lockers of the space shuttle. When mouse or rat macrophage colony-forming units were measured with
this hardware in ground-based assays, we found significantly more colony growth than that seen in standard plate assays. The
improved growth correlates with increased agar thickness but also appears to be due to properties inherent to the Fluid Processing
Apparatus. This paper describes an improved method for determining bone marrow macrophage precursor numbers in semisolid agar. |
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Keywords: | colony-forming unit bone marrow cells macrophage differentiation |
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