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Both stains were visualized by goat anti mouse Alexa Fluor 488 (Invitrogen, Molecular Probes) at a concentration of 1∶1000.
Stains were visualized by 3,3-diaminobenzidine (Dako), with Mayer's hematoxylin (Sigma) as a counter stain, and mounted.
Histological stains were visualized by fluorescence microscopy on an AX70 (Olympus) and digital images were captured and processed using Magnafire (Optronics) and Photoshop (Adobe) software.
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Staining was visualized by Zeiss microscope and analyzed by Image-Pro plusoftwarere.
Staining was visualized by 3,3'-Diaminobenzidine.
Actin staining was visualized by fluorescent microscopy at 40X magnification.
Islet staining was visualized by using a nickel/cobalt enhanced diaminobenzidine solution.
Subsequently the staining was visualized by applying ABC complex and DAB solution.
Staining was visualized by 3-amino-9-ethylcarbazole (AEC) followed by a hematoxylin (Sigma, St . Louis MO) nuclear counterstaining.
Positive staining was visualized by applying 3-amino-9-ethylcarbazole (AEC, Sigma); nuclei were counterstained with haematoxylin.
Staining was visualized by incubation with Alexa-Fluor secondary conjugates (Invitrogen) for 10 minutes at room temperatures.
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