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Liquid dab plus substrate chromogen system

Manufactured by Agilent Technologies

The Liquid DAB plus Substrate Chromogen System is a laboratory reagent designed for use in immunohistochemistry (IHC) and other related techniques. It provides a chromogenic detection solution to visualize the presence and localization of target proteins or antigens in biological samples. The system utilizes 3,3'-Diaminobenzidine (DAB) as the chromogen, resulting in a brown staining reaction. This product is intended for research and investigational use only.

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2 protocols using liquid dab plus substrate chromogen system

1

Immunohistochemistry Analysis of NRCAM in PCa

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Immunohistochemistry was performed on the tissue sections of TMAs of the patients with PCa to gauge the expression levels of NRCAM. Following deparaffinization and dehydration, sections were processed to reveal antigens using a microwave oven. Briefly, the sections were blocked and then incubated with primary antibody against NRCAM (1:100, cat. no. ab87427; Abcam). The slides were subsequently incubated with anti-rabbit secondary antibody and visualized by DakoCytomation Liquid DAB plus Substrate Chromogen System (DakoCytomation).
Two pathologists, who were blind to patient data independently evaluated the TMA samples. The immunohistochemistry score was calculated by the sum of the staining intensity and the fraction of positive tumor cells as previously described (11 (link)–13 (link)).
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2

Calbindin Immunostaining of Brain Sections

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Brain sections were rinsed in 0.05 M PBS containing 1% Triton X-100 (PBST) and placed in 0.6% H2O2 in PBST for 30 min at room temperature. The sections were then placed in 5% normal goat serum in PBST for 1 h at room temperature and were reacted with a mouse monoclonal anti-calbindin antibody (1:15,000; C9848; Sigma-Aldrich; RRID: AB_476894) in 5% normal goat serum-containing PBST at 4°C over two nights. After rinsing in PBST, the sections were reacted with peroxidase-labeled polymer conjugated to goat anti-mouse immunoglobulin (K4001, Dako, Carpinteria, CA, USA) for 1 h at room temperature. Calbindin immunoreactivity was visualized with a chromogenic substrate, 3,3′-diaminobenzidine (liquid DAB plus substrate chromogen system, Dako). Immunostained sections were mounted on gelatin-coated glass slides, air dried, dehydrated in ascending ethanol, cleared with xylene, and cover-slipped with a mounting medium.
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