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Dp11 camera

Manufactured by Olympus
Sourced in Japan

The DP11 camera is a high-quality digital camera designed for use in microscopy and other scientific applications. It features a high-resolution sensor and advanced image capture capabilities to provide detailed and accurate visual documentation of specimens and samples.

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4 protocols using dp11 camera

1

FTO Immunohistochemical Staining Protocol

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Paraffin-embedded sections (4 µm thick) on polylysine-coated slides were used for staining. Antigen retrieval was achieved with 10 mmol/L sodium citrate (pH 6.0). Thereafter, sections were blocked with 10% normal goat serum and then incubated with rabbit monoclonal antibody against FTO (EPR6895, Abcam, 1:1000) overnight at 4 °C. After incubation with secondary antibody (Vector Laboratories), staining was performed using the DAB Substrate Kit for Peroxidase (Vector Laboratories). FTO expression was evaluated by the immunodetection of staining intensity and the number of positive cells. Photomicrographs were imaged using an Olympus BX53 microscope with plan apochromatic objective lenses. An Olympus DP11 camera and Olympus Camedia software were used to produce the images. All cases were reviewed by two pathologists who were blinded to the study and the images were quantified using Image Pro Process software.
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2

Evaluating Tumor Angiogenesis and Cell Dynamics

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Fifteen micron sections of optimal cutting temperature compound-embedded (Tissue-Tek; Sakura Finetek) tumors were immunostained with anti-CD31 antibodies to assess microvessel density (MVD). To quantify MVD, the number of immunostained vessels in ten 0.159 mm2 fields at a magnification of × 100 from ten randomly selected tumors in each group was counted. Five micrometer sections of paraffin-embedded tumor tissue were immunostained with anti-p-Ser10 histone H3 or cleaved PARP antibodies to assess tumor-cell proliferation and apoptosis, respectively, based on the percentage of p-Ser10 histone H3-positive and cleaved PARP-positive cells per ≥500 cell region, respectively. Three tumors per treatment and four regions per tumor were analyzed for tumor cell proliferation and apoptosis. Induction of apoptosis was defined as a two-fold or greater increase in the proportion of cells identified as cleaved PARP-positive in tumors from regorafenib-treated mice compared with tumors from vehicle-treated animals. Images were recorded using an Olympus BX60 microscope equipped with an Olympus DP11 camera. All experiments were performed in triplicate.
Tumor necrosis was assessed by microscopic examination of hematoxylin and eosin (H&E)-stained tumor sections, with ten random fields examined at a × 100 magnification. Tumor necrosis was only qualitatively assessed.
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3

Cave Dwelling Insect Photography

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Live specimens were taken from the caves and brought to the laboratory where they were placed in a terrarium with cave substrate. Before being photographed, the specimens were placed in a Petri dish with cave substrate and left for a few minutes in a refrigerator. Photographs were taken with an Olympus DP11 camera coupled to an Olympus SZH10 stereomicroscope. The insects were kept in the dark and only the cold light of the transilluminator was used.
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4

Measurement of Intestinal Morphology in Piglets

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Gut morphology tissue samples were collected from the duodenum (10 cm from the pylorus), the jejunum (5.5 m from the pylorus), and the ileum (60 cm before the ileo-caecal valve), and processed as described elsewhere [16 (link)]. Briefly, the tissue samples were fixed in 10% neutral buffered formalin and embedded in paraffin wax for microscopic examination of the intestinal villi and crypts. A BX 511 microscope (Olympus, Tokyo, Japan) was used, and the images were digitally captured using a DP 11 camera (Olympus, Tokyo, Japan) under a magnification of 40×. The height and width of the villi and the depth of the crypts were measured using the DP-Soft software (Olympus). Ten intact and properly oriented villi and crypts from each intestinal region were selected per piglet.
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