For the cell biologist, identifying changes in gene expression using DNA mi
croarrays is,just the start of along journey from tissue to cell. We discus
s how chip users can first filter noise (false-positives) from daunting mic
roarray datasets. Combining laser capture microdissection with real-time po
lymerase chain reaction and reverse transcription is a helpful follow-up st
ep that allows expression of selected genes to be quantified in populations
of recovered cells. The voyage from chip to single cell can be completed u
sing sensitive new in situ hybridization and immunohistochemical methods ba
sed on tyramide signal amplification.