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Rouet-Benzineb et al. [ 38] demonstrated the colocalization of MMP2 and MMP9 in LV myocardium from patients with idiopathic DCM using a confocal microscopic immunoreactive staining.
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Microscopic images of fluorescence were collected using a confocal microscope equipped with the Laser Scanning Microscope 5 PASCAL program (Carl Zeiss).
Endfoot sizes were analyzed using a confocal microscope (SP5, Leica; objective, HCX PL APO CS 63X oil UV corrected; aperture, 1.4; microscopic zoom, 5 to ×13; scanning frequency, 100 Hz; average: 4 times and pinhole, 0.5 AU with a z-stack over 20 µm with a step size of 0.5 µm).
Images were captured using a confocal microscope (Leica FV1000).
Cells were then imaged using a confocal microscope (LSM780, Zeiss).
Cell development and status were monitored using a confocal microscope.
Images are obtained using a confocal microscope.
Staining was visualised using a confocal microscope.
Images were taken using a confocal microscope.
The second method used a confocal microscope.
Microscopic analysis was performed using a confocal laser-scanning microscope (Zeiss LSM 710 META, Germany).
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