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Aec substrate solution

Manufactured by Vector Laboratories

AEC substrate solution is a reagent used in immunohistochemistry and enzyme-linked immunosorbent assays (ELISA) to visualize the presence of target proteins or antigens. The solution contains 3-amino-9-ethylcarbazole, which is an enzymatic substrate that produces a reddish-brown color upon reaction with the enzyme label, typically horseradish peroxidase. This substrate solution is used to develop and detect the signal in these immunoassay techniques.

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3 protocols using aec substrate solution

1

Histological Analysis of Imiquimod-Induced Skin Inflammation

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Skin sections from IMQ-treated skin were embedded and frozen in OCT and stained with H&E and Gr-1 mAb for IHC. Epidermal thickness was determined by measuring the average interfollicular distance under the microscope in a blinded manner. For IHC staining, skin cryosections were fixed, blocked and then stained with purified rat-anti-mouse Gr-1 Ab (1:50 dilution) following with goat-anti-rat IgG secondary antibody (1:200 dilution, Southern Biotech). Slides were developed with AEC substrate solution (Vector Laboratories) and then counterstained with hematoxylin. Images were acquired at x200 magnification using Aperio ScanScope digital scanners.
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2

Histological Analysis of Epidermal Thickness

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Skin sections were stained with H&E. Epidermal thickness was determined by measuring the mean interfollicular distance under the microscope. For IHC staining, skin cryosections were fixed, blocked, and stained with purified rabbit-anti-mouse Ki-67 Ab (1:200 dilution), followed by anti-rabbit IgG secondary antibody (1:200 dilution). Slides were developed with AEC substrate solution (Vector Laboratories) and then counterstained with hematoxylin. Images were acquired at 200× magnification using a Keyence BZ-X800 microscope.
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3

Histological Analysis of Imiquimod-Induced Skin Inflammation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Skin sections from IMQ-treated skin were embedded and frozen in OCT and stained with H&E and Gr-1 mAb for IHC. Epidermal thickness was determined by measuring the average interfollicular distance under the microscope in a blinded manner. For IHC staining, skin cryosections were fixed, blocked and then stained with purified rat-anti-mouse Gr-1 Ab (1:50 dilution) following with goat-anti-rat IgG secondary antibody (1:200 dilution, Southern Biotech). Slides were developed with AEC substrate solution (Vector Laboratories) and then counterstained with hematoxylin. Images were acquired at x200 magnification using Aperio ScanScope digital scanners.
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