Staining Kit: Silver Method after CAMPBELL-SWITZER
Article no.: 16854
Neurofibril staining
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product information
Components of this kit:
• Horn softener for histology, Artikel-Nr.:14835
• Citric Acid 1 %, Artikel-Nr.:16827
• Acetate buffer pH 4.99 (stock solution), Artikel-Nr.:16859
• Sodium Thiosulfate 1 %, Artikel-Nr.:11155
• Kit: Silver Pyridine Carbonate acc. to CAMPBELL-SWITZER, Artikel-Nr.:16898
• Developing Solution for CAMPBELL-SWITZER Staining, Artikel-Nr.:16903
Instructions / Protocol / Recommendations
Verwendung:
The staining kit: silvering according to CAMPBELL-SWITZER is a solution used especially for in vitro diagnostics of neurological diseases. This solution is mainly used in the staining of neurofibrils, which are relevant in the study of Alzheimer pathologies. By using this staining kit, neurofibrils can be visualized in cellular structures and tissue samples, allowing successful differentiation and analysis of healthy and pathologically altered tissue. This supports research into these diseases and helps in the development of diagnostic and therapeutic approaches.
Prinzip:
Campbell-Switzer silver plating is a staining method used in in vitro diagnostics for visualization and identification of tissue or cell structures, especially in the study of Alzheimer's pathologies. The principle of operation is based on the attachment of silver ions contained in the silver pyridine carbonate solution to specific structures in the tissue, such as amyloid plaques and neurofibrillary bundles. The binding of the silver ions to these structures allows their visualization under the microscope. The other solutions, such as ammonia, citric acid, acetate buffer, and sodium thiosulfate, are used to stabilize, activate, and reduce the silver ions in the tissue. The developer solution enhances the staining to make the structures more visible. Overall, this technology enables improved analysis of Alzheimer's-associated changes in brain tissue.
Verfahren:
Campbell-Switzer silver plating is a staining method used in in vitro diagnostics for visualization and identification of tissue or cell structures, especially in the study of Alzheimer's pathologies. The principle of operation is based on the attachment of silver ions contained in the silver pyridine carbonate solution to specific structures in the tissue, such as amyloid plaques and neurofibrillary bundles. The binding of the silver ions to these structures allows their visualization under the microscope. The other solutions, such as ammonia, citric acid, acetate buffer, and sodium thiosulfate, are used to stabilize, activate, and reduce the silver ions in the tissue. The developer solution enhances the staining to make the structures more visible. Overall, this technology enables improved analysis of Alzheimer's-associated changes in brain tissue.
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