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Diazonium fast blue rr salt

Manufactured by Merck Group

Diazonium fast blue RR salt is a chemical compound used in various analytical and synthetic applications in laboratory settings. It serves as a versatile reagent for the detection and identification of certain functional groups and compounds. The core function of this product is to provide a colorimetric response when reacting with specific analytes, enabling researchers to perform various chemical analyses and assays.

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3 protocols using diazonium fast blue rr salt

1

Osteoclast and Osteogenic Cell Evaluation

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TRAP was used to evaluate osteoclasts by using 2.5 mM naphthol AS-TR phosphate (Sigma-Aldrich), 0.36 M N-N-dimethyl-formamide (Sigma-Aldrich), and 4 mM salt in pH 5.2 acetate buffer. Nonosteoclastic acid phosphatase activity was inhibited with 100 mM l(+)-tartaric acid (Sigma-Aldrich) added to the substrate solution.
ALP was used to reveal the layer of osteogenic cells (pre-osteo/cementoblasts and osteo/cementoblasts) by incubating the sections with naphthol-ASTR-phosphate (Sigma-Aldrich) and diazonium Fast Blue RR salt (Sigma-Aldrich) for 30 min at 37°C (pH 9) in the presence of MgCl2.
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2

Histological Analysis of Osteogenic Differentiation

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Samples were fixed in 4% paraformaldehyde and embedded in paraffin for sectioning (n = 6 per group). Seven micrometer thick serial sections were dewaxed, rehydrated and stained with von Kossa staining, Sirius Red, processed for alkaline phosphatase (ALP) activity used as a marker of osteogenic cell differentiation. Histology sections were incubated with naphthol ASTR phosphate (Sigma–Aldrich, St. Louis, MO) and diazonium fast blue RR salt (Sigma–Aldrich) for 30 minutes at 37°C (pH 9) in the presence of MgCl2. Alizarin Red was used as a mineralization marker, showing specifically calcium ions. The slides were rinsed, dehydrated and mounted for observation with an optical microscope (Nikon E600 POL) or an epifluorescence microscope (AXIO 100 Zeiss). Marked cells (ALP) and calcium deposits (Alizarin Red) were quantified using ImageJ software (six sections were counted for each sample).
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3

Osteoclast and Osteogenic Cell Evaluation

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Tartrate-resistant acid phosphatase (TRAP) was used to evaluate osteoclasts by using 2.5 mM naphthol-ASTR-phosphate (Sigma–Aldrich), 0.36 M N–N-dimethyl-formamide (Sigma–Aldrich), and 4 mM salt in pH 5.2 acetate buffer. Non-osteoclastic acid phosphatase activity was inhibited with 100 mM L(+)-tartaric acid (Sigma–Aldrich) added to the substrate solution.
Alkaline phosphatase was used to reveal the layer of osteogenic cells by incubating the sections with naphthol ASTR phosphate (Sigma–Aldrich) and diazonium fast blue RR salt (Sigma–Aldrich) for 30 min at 37°C (pH 9) in the presence of MgCl2.
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