Confocal microscopy and histological analysis

ML Moon Young Lee
CP Chanjae Park
SH Se Eun Ha
PP Paul J. Park
RB Robyn M. Berent
BJ Brian G. Jorgensen
RC Robert D. Corrigan
NG Nathan Grainger
PB Peter J. Blair
OS Orazio J. Slivano
JM Joseph M. Miano
SW Sean M. Ward
TS Terence K. Smith
KS Kenton M. Sanders
SR Seungil Ro
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Tissues were analyzed by cryostat section staining using confocal microscopy as previously described [5]. Jejunum and colon tissues were double stained with anti-SRF (1:500, Santa Cruz Biotechnology, Dallas, TX) and anti-αSMA (1:1200, Sigma, St. Louis, MO) antibodies. Stained tissues were analyzed using confocal microscopy. For histological analysis, tissues were dehydrated, embedded in paraffin, cut into 4 μm-thick coronal sections, rehydrated and stained with H&E. Images were collected using an Olympus FV1000 confocal laser scanning microscope with Fluoview FV10-ASW 3.1 Viewer software (Olympus, Tokyo, Japan) or the iScan Coreo scanner (Ventana Medical Systems, Tucson, AZ).

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