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Ar0038

Manufactured by Boster Bio

The AR0038 is a laboratory equipment product from Boster Bio. It is designed for scientific research and analysis purposes. The core function of the AR0038 is to provide accurate and reliable measurement capabilities for researchers and scientists.

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2 protocols using ar0038

1

Immunohistochemical Staining Protocol

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Slides (4 μm) were dewaxed in transparency agent and rehydrated in ethanol prior to antigen retrieval. Antigen retrieval was conducted by steaming slides in 1X EDTA buffer (Beyotime, #P0085) for 15 min by microwave irradiation (500 W). Endogenous peroxidase was quenched by treating samples with 3% H2O2 for 10 min. After the above steps, 5% goat serum (BOSTER, #16K03A09) was added onto slides for blocking, 30 min later, followed by staining in primary antibodies overnight at 4 °C. After a 1 h rewarming phase, secondary antibody was applied prior to DAB treatment (Zhongshanjinqiao, #ZLI-9108) for 1 h at RT. Hematoxylin was used for counterstain, then slides rinsed in running water for 5 min and differentiated with 1% hydrochloric acid alcohol for 2 s until the nuclei returned to blue. The tissues were dehydrated with graded ethanol and mounted with neutral resin (BOSTER, AR0038). Images were photographed by inverted microscopy and analyzed using IPP software.
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2

Histological Analysis of Lung Tissues

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Lung and airway tissues were fixed with 4% paraformaldehyde (R008069, Rhawn) for 24 h at room temperature. Then the samples were washed overnight with tap water and dehydrated with gradient ethanol (E809057, Macklin, Shanghai, China) and double distilled water. Subsequently, the tissues were embedded into paraffin, sectioned, and dewaxed. Then the tissues or cells in BALF were stained by hematoxylin (B25380, Yuanye, Shanghai, China) for 10 min and further incubated with hydrochloric acid alcohol (AR0038, Boster, Wuhan, China, http://www.boster.com.cn/index/index.html) for 5 min. Then the samples rested in 50°C warm bath until the tissues appeared blue, and were further stained with eosin (C0109, Beyotime) for 1 min at room temperature. After soaking the samples in gradient ethanol again for dehydration, the sample slices were made transparent by soaking in xylene (R017750, Rhawn). Finally, the sample slices were sealed with neutral gum (N116470, Aladdin, Shanghai, China) and the image of each section was collected under a DMLA full automatic microscope (Leica, Solms, Germany) at a magnification of 100 ×.
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