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Icc50 hd light microscope

Manufactured by Leica

The ICC50 HD is a light microscope designed for high-definition imaging. It features a high-definition camera and advanced optics to produce clear, detailed images of samples. The core function of the ICC50 HD is to enable the observation and documentation of microscopic specimens.

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4 protocols using icc50 hd light microscope

1

Histological Analysis of Marine Invertebrate Tissues

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Thirty samples, comprising 15 from each group, were collected. The gills, intestine, stomach, hepatopancreas, and female gonad were promptly excised and fixed in a 10% formalin solution for 24 h. Subsequently, the samples underwent a thorough process, including washing with distilled water, dehydration with a series of ethyl alcohol concentrations (70%, 80%, 90%, 95%, and 100%), overnight immersion in methyl benzoate, and two rounds of clearing with xylene. Following these preparations, the samples were fixed in 65–70 °C paraffin, sliced into sections of 5–6 μm, and stained with hematoxylin/eosin. The examination of the samples was conducted using a Leica® ICC50 HD light microscope.
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2

Intestinal Morphology in Embryonic Fish

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Morphological changes in the intestines of embryonically exposed fish were examined by hematoxylin and eosin (H&E) staining (n=6 fish per exposure per sampling time point). Sections were stained with H&E and imaged using a Leica ICC50 HD light microscope. ImageJ software (National Institute of Health) was used to determine height and width (mm) of 5 villi per field of view.
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3

Muscle Fiber Density Quantification

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Sections of trunk muscle directly posterior to the dorsal fin were collected (4–8 fish per tank; n=7 tanks per exposure group) and fixed in 10% neutral-buffered formalin for 18 hours, progressively dehydrated in ethanol, and paraffin-embedded. Blocks were cut into 7 μm sections and one muscle trunk sample per tank at 16 weeks was used for hematoxylin and eosin (H&E) staining (n=6 fish per exposure group). Once the fish could be sexed, approximately 3 males and 3 females per tank were taken for muscle fiber density quantification at 28, 40 and 52 weeks. Slides were imaged using a Leica ICC50 HD light microscope and Leica EZ suite software. ImageJ software (National Institutes of Health) was used to count muscle fibers. Upper right quadrants of each tissue section were selected for quantification and areas were determined (mm2) to calculate density (fibers/mm2). Average densities for all fish and males/females were determined for each tank.
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4

Characterization of Bacterial Isolates

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The test isolates were subjected to conventional tests for pH, temperature, and salt (NaCl) requirements in growth media. The pH, temperature and NaCl requirements for bacterial growth were measured in Nutrient Broth (NB) media at 600 nm wavelength in spectrophotometer 13 . Firstly, NB media were prepared and, then a full loop of each test isolate on NA was transferred to broth media and incubated at different temperatures (4-35°C) for 48 hours. To measure the response to pH changes during growth, NB media were prepared and pHs of broth media were adjusted to different points in pH 3-11 range, before autoclaving. Then, a full loop of each test isolate on NA was transferred to broth media and incubated at 15°C for 48 hours. The salt (NaCl) requirement for growth was also tested in NB media containing 2-15 (w/v). To this aim, NB media were prepared and salt at predetermined concentrations was added to broth media for each isolate, before autoclaving. Then, a full loop of each test isolate on NA was transferred to broth media and incubated at 15°C for 48 hours. For each test, microbial growth was measured at 600 nm wavelength at the end of the incubation period. Cell and colony morphology (Leica ICC50 HD light microscope), Gram and endospore staining, motility and the presence of catalase and oxidase reactions were also investigated [13] [14] (link)[15] (link) .
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