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Dp controller and manager software

Manufactured by Olympus
Sourced in Japan, United States

The DP Controller and Manager software is a digital imaging solution that provides camera control and image management functionalities. It enables users to capture, preview, and process digital images from compatible Olympus microscope cameras.

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3 protocols using dp controller and manager software

1

Lung Tissue PAS Staining Protocol

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Periodic Acid-Schiff (PAS) staining was performed in the formalin-fixed/paraffin-embedded lung tissues. Tissue sections were examined with an Olympus BX40 microscope in conjunction with an Olympus U-TV0.63XC digital camera (Olympus Corp., Melvile, NY). Images were acquired using DP Controller and Manager software (Olympus Corp.).
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2

Immunohistochemical Detection of VP2 Protein

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Differentiated cell cultures were fixed with 10% normal-buffer formalin, and embedded in paraffin (University of Wisconsin Histology Lab, Madison, WI). Five μm sections were adhered to slides which were deparaffinized and then rehydrated. For antigen retrieval, slides were incubated with proteinase K (40 μg/mL in PBS, 10 min, 37 °C). Peroxidases were blocked (5 min, RT) with Peroxidazed 1 (Biocare Medical, Concord, CA). Slides were blocked (3% FBS, 2% goat serum, 0.2% Tween-20, 1.25% Human BD Fc Block™, 1 h, RT), incubated (1:200 in blocking buffer, 2 h, RT) with anti-C15-VP2 mouse monoclonal antibody (kindly provided by MedImmune Inc., Gaithersberg MD), Mach 4 Universal Probe and then Polymer (15 min, RT each, Biocare Medical, Concord, CA), Betazoid DAB (5 min, RT, Biocare Medical, Concord, CA), and counterstained with CAT hematoxylin or eosin (30s, RT, Biocare Medical, Concord, CA). Images from labeled slides were acquired and analyzed using an Olympus BX60 light microscope with DP Controller and Manager software (Shinjuku-ku, Tokyo, Japan).
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3

Quantifying Goblet Cell Hyperplasia

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After BAL fluid collection, the left lung was inflated with 10% formalin at a standard pressure. Lung tissues were then embedded in paraffin, and 3-µm-thick sections were cut and stained with periodic acid-Schiff (PAS) to determine goblet cell hyperplasia. Stained tissue sections were examined with an Olympus BX40 microscope in conjunction with an Olympus U-TV0.63XC digital camera (Olympus Corp., NY, USA). Images were acquired using DP Controller and Manager software (Olympus Corp., NY, USA). The number of PAS-positive cells per millimeter of bronchial basement membrane (mmBM) was measured by MetaMorph 4.6 (Universal Imaging, PA, USA).
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