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Vbs refine polymer detection system

Manufactured by Leica

The VBS Refine polymer detection system is a laboratory equipment product offered by Leica. It is designed to detect and analyze polymers in various samples. The system provides accurate and reliable results for polymer identification and characterization.

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3 protocols using vbs refine polymer detection system

1

Immunohistochemical analysis of aortic tissue

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All aortic tissue cross-sections from the above experiments were prepared with a Bond-Max autostainer (Leica Microsystems, Wetzlar, Germany). Slides were stained with primary antibody on a fully automated Bond-Max system and VBS Refine polymer detection system (Leica Microsystems) as previously described (Lo et al., 2017 (link)). Negative controls did not contain primary antibody. Positive immunoreactivity signals in the endothelial layers were measured by ImageJ software. Immunoreactivity signals in endothelial layers from TNF-α and the TNF-α+LSM, TNF-α+LSM+Ab, or TNF-α+rbFGF groups were quantified as previously described (Federici et al., 2002 (link)).
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2

Aortic Tissue Immunohistochemistry in db/db Mice

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For aortic tissue sections from db/db mice, 3,3′-diaminobenzidine staining was performed using a Bond-Max autostainer (Leica Microsystems). Briefly, paraffin-embedded aortic tissue sections were placed in Tris buffered saline with Tween-20, then rehydrated through serial dilutions of alcohol, and washed with PBS (pH 7.2). Slides were then stained with primary antibodies against IRAK-1 (dilution 1:50, mouse monoclonal antibody, Santa Cruz), or ICAM-1 (dilution 1:50, mouse monoclonal antibody, Thermo Fisher), or incubated with PBS (as a negative control) on a fully automated Bond-Max system using onboard heat-induced antigen retrieval and a VBS Refine polymer detection system (Leica Microsystems).
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3

Immunohistochemical Analysis of Neuroendocrine Markers

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Hematoxylin and eosin staining results of all 21 samples were reviewed by two pathologists. The specimens were fixed in formalin and embedded in paraffin before they were archived. We used the archived specimens for immunohistochemical analysis. Immunohistochemical staining was performed with Bond-Max autostainer (Leica Microsystems, Wetzlar, Germany), using CD56 (NCL-CD56-1B6, clone 1B6; 1:15; Novocastra/Leica, Newcastle-upon-Tyne, UK), chromogranin (NCL-CHROM-430, clone 5H7; 1:50; Novocastra/Leica), synaptophysin (NCL-SYNAP-299, clone 27G12; 1:50; Novocastra/Leica), and neuron-specific enolase (BBS/NC/VI-H14; 1:200; Dako, Carpinteria, CA, USA). Briefly, specimens from the paraffin-embedded blocks were cut into 5-μm sections. The sections were dewaxed in a 60°C oven, deparaffinized in xylene, rehydrated through serial dilutions of alcohol, and washed in phosphate-buffered saline (pH 7.2). Immunohistochemical staining was performed in the fully automated Bond-Max autostainer using onboard, heat-induced antigen retrieval in citrate buffer according to the ER1 protocol for 20 minutes and a VBS Refine polymer detection system (Leica Microsystems). Diaminobenzidine was used as the chromogen (Leica Microsystems). The sections were then counterstained with hematoxylin.
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