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Mucicarmine

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Catalog No. T86937Cas No. 51395-97-2

Mucicarmine is utilized in histology to visualize acid mucopolysaccharides in tissue sections. It identifies mucin (deep rose), aiding in the detection of mucin-positive cancers such as liver carcinoma [1].

Mucicarmine

Mucicarmine

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Catalog No. T86937Cas No. 51395-97-2
Mucicarmine is utilized in histology to visualize acid mucopolysaccharides in tissue sections. It identifies mucin (deep rose), aiding in the detection of mucin-positive cancers such as liver carcinoma [1].
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Product Introduction

Bioactivity
Description
Mucicarmine is utilized in histology to visualize acid mucopolysaccharides in tissue sections. It identifies mucin (deep rose), aiding in the detection of mucin-positive cancers such as liver carcinoma [1].
In vitro
Mucicarmine effectively stains mucin on frozen-tissue sections, appearing deep rose. To perform the staining, mount cryostat sections (4 to 5 μm thick) onto coated glass slides. Fix these sections in frozen-section fixative for 30 seconds, then rinse with water for 5 seconds. Immerse the slides in Harris hematoxylin for 30 seconds, followed by 5-second immersions in distilled water, ammonium hydroxide, and distilled water. Heat the mucicarmine stain in a microwave until it is about to bubble (approximately 30 seconds). Submerge the slides in the warmed mucicarmine solution for 2 minutes and rinse with distilled water for 5 seconds. Sequentially dip the slides in 95% alcohol, 100% alcohol, and xylene for 5 seconds each before coverslipping. Note: Nuclei (blue) and connective tissue (green) staining may be necessary based on specific requirements.

The above information is based on published literature. Experimental procedures should be appropriately modified to meet specific research demands.
Chemical Properties
Cas No.51395-97-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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