An overview of the immunocolloidal-gold technology
Technology based upon immunocolloidalgold (often called “colloidal”) is used to identify new types of antigen markers. Faulk equals 1971 immunochemical introduced the colloidalgold by Faulk. In 1980, Leuvering published a colloidal-gold method of immunology Leuvering first reported on using the colloidal uptake of human chorionicgonadotropin (mCG) for agglutination testing. This technology is being rapidly used in areas such as medical clinical inspection, food security inspection, and animal epidemic surveillance. Coloidal gold immunofiltration (CGI) and colloidal Gold immunochromatography (CGI) are two of the most popular and widely used techniques within the veterinary industry.
Coloidal gold immunolabeling technology
The colloidal gold, which is positively charged when placed in weak bases environment, can form an electrical bond with negatively charged proteins molecules. It does not alter the biochemical properties of the proteins. Due to the high amount of surface charge, colloidal silver particles are strong at binding proteins. To make colloidal golden proteins, you can noncovalently combine coloidal gold particles with staphylococcus A (SPA), staphylococcus A (IgG), toxin, toxin and hormone, as well as bovine serumalbumin peptide conjugate. If the markers are made from gold particles of high electron densities, visible pink spots could be formed when they aggregate at an antigen body reaction spot on the solid-phase carrier. Therefore, colloidal gold, as a marker, can be used in immunoelectron microscopy, conventional light microscopy, quantitative and qualitative studies of antigens, as well as qualitative or semi-quantitative rapid detection of antigens or antibodies in vitro immunochromatography.
Benefits of the colloidal-gold immunolabeling technique
Immunocolloidal-gold technology is stable and easy to preserve. It is possible to preserve the results of experiments for long periods. This operation is quick and easy. The results can also be easily observed and compared. It is as simple as immersing the strips into the specimen. After the immunoanalysis, the colloidal gold will be used to indicate the process of forming the color mark. The whole process takes between 3-10 minutes. It’s not harmful to the operator. There are no radioisotopes and o-phenylenediamines which can pollute the environment or cause harm to the operator in colloidal silver immunodetection. There is no harm in gold or silver, and there are no environmental pollutants. The commercial reagent doesn’t require any instruments, which saves money, makes it easier to use, and allows for more field applications.
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