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Basms 2325

Manufactured by Fujifilm
Sourced in Japan

The BASMS-2325 is a high-performance laboratory equipment designed for precise and efficient sample processing. It features advanced technology to ensure consistent and reliable results. The core function of this product is to facilitate the preparation and handling of samples in a controlled laboratory environment.

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24 protocols using basms 2325

1

Cardiac Radiotracer Distribution Analysis

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After euthanasia, animals were perfused and heart samples were excised. To determine radiotracer distribution, digital autoradiography was performed by placing tissue samples in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm) for 12.5 hours at −20 °C. Phosphorimaging plates were read at a pixel resolution of 25 μm with a Typhoon 7000IP plate reader (GE Healthcare). Quantification was carried out using ImageJ software.
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2

Zirconium-89 Distribution in Aorta and Infarct

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Digital autoradiography was performed to determine Zirconium-89 distribution within the whole aorta and infarct. Samples were placed in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm) for 1.5 h (whole aortas) or, 2h (hearts) and stored at −20 °C. Phosphorimaging plates were read at a pixel resolution of 25 μm with a Typhoon 7000IP plate reader (GE Healthcare). Quantification was carried out using ImageJ software.
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3

Digital Autoradiography of Tissue Samples

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Tissue samples were placed in a film cassette against a phosphorimaging plate to perform digital autoradiography (BASMS-2325, Fujifilm, Valhalla, NY) for 48 hours at −20 °C. The phosphorimaging plates were set at a pixel resolution of 25 μm with a Typhoon 7000IP plate reader (GE Healthcare, Pittsburgh, PA).
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4

Targeted Radionuclide Therapy in Xenografted Tumors

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Athymic nude mice xenografted with BxPC3 tumors were injected with either 225Ac-DOTA-PEG7-5B1 (18.5 kBq, 8.6 μg [MA = 308 kBq/nmol]; in 150 μL of 0.9 % NaCl + 1.0 % BSA) or 225Ac-DOTA-PEG7-Tz (18.5 kBq, 0.4 nmol [MA = 46 kBq/nmol]; in 150 μL of 0.9 % NaCl + 1.0 % BSA) at 72 h post administration of 5B1-TCO (200 μg; in 200 μL of PBS). Mice were euthanized 1, 5, and 7 d post-injection of the radiopharmaceutical. Mouse kidneys and tumors were embedded and sectioned during the 20 minutes that followed the animal sacrifice. Kidney and tumor sections were placed in a film cassette against a phosphor imaging plate (Fujifilm BAS-MS2325) for a first exposure time of 1 hour at −20 °C. A second exposure (6 hours) with the same sections was performed once secular equilibrium was reached (24 h after first exposure). Kidney sections were later stained with hematoxylin and eosin for the differentiation of the cortex and medulla. Images analysis and quantification is described in Supporting Information.
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5

Autoradiographic Analysis of Aortic Tissues

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Following radioactivity counting, aortas were placed in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm, Valhalla, NY) for 24 hours at −20 °C in order to determine radioactivity distribution. The plates were read at a pixel resolution of 25μm with a Typhoon 7000IP plate reader (GE Healthcare, Pittsburgh, PA).
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6

Radioactivity Distribution Analysis

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Tissues were placed in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm) at −20 °C to determine the radioactivity distribution. The plates were read at a pixel resolution of 25 mm with a Typhoon 7000IP plate reader (GE Healthcare).
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7

Quantifying Tumor Radiotracer Uptake

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Tumors of euthanized animals were excised, submerged in Tissue–Plus OCT compound (Scigen, Gardena, CA), and frozen on dry ice. Series of 10 μm tissue sections were cut and placed in a film cassette beneath a phosphor-imaging plate for 48–72 h at − 20 °C (BASMS-2325; Fujifilm, Tokyo, Japan), which was then read on a Typhoon 7000IP plate reader (GE Healthcare, Chicago, IL) at 25 μm pixel resolution. Several sequential sections were submitted to the Molecular Cytology Core Facility at MSKCC for hematoxylin and eosin and HuMab-5B1 (0.5 μg/ml) staining. Image analysis was performed with ImageJ (https://imagej.nih.gov/ij/).
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8

Radiotracer Distribution in Aortic Tissue

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The perfused and excised aortas were placed
in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm,
Valhalla, NY, USA) for 72 h at −20 °C to determine the
radiotracer distribution. Phosphorimaging plates were read at a pixel
resolution of 25 μm with a Typhoon 7000IP plate reader (GE Healthcare,
Pittsburgh, PA, USA). The images were postprocessed using ImageJ software.
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9

Autoradiographic Analysis of Aortic Tissues

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Following radioactivity counting, aortas were placed in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm, Valhalla, NY) for 24 hours at −20 °C in order to determine radioactivity distribution. The plates were read at a pixel resolution of 25μm with a Typhoon 7000IP plate reader (GE Healthcare, Pittsburgh, PA).
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10

Regional Radioactivity Quantification in Tissues

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Tissues (heart and aorta) were placed in a film cassette against a phosphorimaging plate (BASMS-2325, Fujifilm) at − 20 °C to determine the regional radioactivity distribution. Exposure time was optimized to dose, tracer, and tissue uptake differences. Tissues from the heart of [18F]F-FDG injected animals were exposed for 5 min, [18F]F-FDG infused aortas were exposed for 30 min and tissues from animals in the [64Cu]Cu-DOTATATE group were exposed for 60 min. The plates were read at a pixel resolution of 25 μm with a Typhoon 7000IP plate reader (GE Healthcare, Pittsburgh, PA). Images were analyzed using ImageJ software v1.52 (Madison, WI).
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