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Diaminobenzidine chromogen solution

Manufactured by Agilent Technologies
Sourced in United States

Diaminobenzidine chromogen solution is a laboratory reagent used for the detection and visualization of specific proteins or enzymes in various applications, such as immunohistochemistry and enzyme-linked immunosorbent assays (ELISA). The solution contains diaminobenzidine, a chromogenic substrate that undergoes a color reaction in the presence of the target analyte, producing a visible brown or reddish-brown stain. This solution is commonly used to facilitate the detection and analysis of target molecules in biological samples.

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3 protocols using diaminobenzidine chromogen solution

1

CD68 Immunohistochemistry Staining Protocol

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The immunohistochemistry assay was performed according to Yin et al. (26 (link)). The sections were incubated with the primary antibody of CD68 (Ab955, 1: 100, Abcam, Cambridge, UK) at 4 °C overnight and horseradish peroxidase labeled goat anti-mouse IgG antibody (A205719, 1:200, Abcam, Cambridge, UK) at room temperature for 1 h. The color reaction was performed with diaminobenzidine chromogen solution (Dako, Carpinteria, USA). Brown-yellow particles represented the positive expression of CD68 protein and the blue particles represented the nucleus stained by hematoxylin (Sigma, USA).
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2

Immunohistochemical Analysis of CD68 Expression

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The immunohistochemistry assay was performed according to Yin et al [26] . The sections were incubated with the primary antibody of CD68 (Ab955, 1: 100, Abcam, Cambridge, UK) at 4 °C overnight and horseradish peroxidase labeled goat anti-mouse IgG antibody (A205719, 1: 200, Abcam, Cambridge, UK) at room temperature for 1 h. The color reaction was performed with diaminobenzidine chromogen solution (Dako, Carpinteria, USA). Brown-yellow particles represented the positive expression of CD68 protein and the blue particles represented the nucleus stained by hematoxylin (Sigma, USA).
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3

Immunohistochemical Analysis of CD68 Expression

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The immunohistochemistry assay was performed according to Yin et al [26] . The sections were incubated with the primary antibody of CD68 (Ab955, 1: 100, Abcam, Cambridge, UK) at 4 °C overnight and horseradish peroxidase labeled goat anti-mouse IgG antibody (A205719, 1: 200, Abcam, Cambridge, UK) at room temperature for 1 h. The Color reaction was performed with diaminobenzidine chromogen solution (Dako, Carpinteria, USA). Brown-yellow particles represented the positive expression of CD68 protein and blue particles represented the nucleus stained by hematoxylin (Sigma, USA).
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