Background: Numerous applications of fluorescence microscopy require quantitation of signal intensity in reproducible units. Two problems must be overcome to achieve this goal. First, due to various instrumental factors, the same sample imaged on two microscopes or even on the same microscope at dif
Photoactivation of a Substrate for Cell Adhesion under Standard Fluorescence Microscopes
β Scribed by Nakanishi, Jun; Kikuchi, Yukiko; Takarada, Tohru; Nakayama, Hidekazu; Yamaguchi, Kazuo; Maeda, Mizuo
- Book ID
- 126917471
- Publisher
- American Chemical Society
- Year
- 2004
- Tongue
- English
- Weight
- 169 KB
- Volume
- 126
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract Cell Adhesion Factor, complexed to insoluble collagenβcoated tissue culture dishes, is required for the attachment of fibroblasts to this substrate. In solution, the factor has no demonstrable affinity for cells in suspension following trypsinβEDTA removal of cells from monolayer. Cell
## Abstract High hydrostatic pressure (HHP) becomes more and more interesting for life science research, since it can be employed to inactivate various cells. To directly monitor βcells under pressure,β the development of an optical highβpressure chamber is required. Therefore, an optical pressure
A standardized urinalysis and manual microscopic cell counting system was evaluated for its potential to reduce intraand interoperator variability in urine and cerebrospinal fluid (CSF) cell counts. Replicate aliquots of pooled specimens were submitted blindly to technologists who were instructed to