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Diaminobenzidine dab substrate kit

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The Diaminobenzidine (DAB) Substrate Kit is a laboratory reagent used for the detection of specific proteins or enzymes in biological samples. It provides a chromogenic substrate that, when catalyzed by the target enzyme, produces a brown or black precipitate. This reaction can be visualized using light microscopy, allowing for the localization and quantification of the target analyte within the sample.

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2 protocols using diaminobenzidine dab substrate kit

1

Quercetin Cytotoxicity Evaluation Protocol

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Quercetin (Sigma, USA) was prepared into a 200 mM stock using dimethyl sulfoxide (DMSO) and stored at −20°C. The working concentration of 200 μM Quercetin was made in a complete medium, and a range of concentrations of Quercetin (10, 20, 50, 100, 150 and 200 μM) was utilized in cell viability assay. Cisplatin (Sigma, USA) and paclitaxel (MedChemExpress, USA) were stored at −20°C, while 5-fluorouracil (Solarbio, China) and doxorubicin (Solarbio, China) were stored at 4°C. Primary antibodies for MMP2 (monoclonal rabbit anti-human antibody; 1:1000), ezrin (polyclonal rabbit anti-human; 1:1000) and GAPDH (monoclonal rabbit anti-human antibody; 1:1000) were purchased from Cell Signaling Technology, and P-Gp (monoclonal rabbit anti-human antibody; 1:1000) and METTL3 (monoclonal rabbit anti-human antibody; 1:1000) were purchased from Abcam (1:1000, USA); and the second antibody, peroxidase-conjugated goat anti-rabbit antibody, was obtained from Biosharp (1:5000, USA). Diaminobenzidine (DAB) Substrate Kit was purchased from Zhongshan Goldenbridge (China).
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2

Propofol Cytotoxicity Assay Protocol

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Propofol (Sigma, USA) was stored at room temperature, and two series of various concentrations of Propofol (clinically relevant concentrations: 0, 5, 10, 20, 40, and 80 μM; high concentrations: 0, 100, 200, 400, 600, and 800 μM) were applied in the cell viability assay. Paclitaxel (MedChemExpress, USA) was stored at −80°C. The diaminobenzidine (DAB) substrate kit was obtained from Zhongshan Goldenbridge (China). The primary antibodies utilized were as follows: rabbit anti‐β‐tubulin (1:2000, ABclonal, AC008, China), rabbit anti‐stathmin 1 (1:1000, Abcam, ab52630, USA) and rabbit anti‐GAPDH (1:2000, CST, #5174, USA). The secondary antibody was a horseradish peroxidase‐conjugated goat anti‐rabbit antibody (1:2000, Biosharp, USA).
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