Buffers

Features 0.25M Tris, 1.92M Glycine, pH 8.3

Features 0.25M Tris, 1.92M Glycine, pH 8.3

Features 1M Tris, 1M Tricine, 1% SDS, pH 8.3

Features 1M Tris, 1M Tricine, pH 8.3

The Trypsin Digestion Mix provides optimal buffered conditions for in gel trypsin digestion of proteins. Suitable for 100 protein spots.

The conjugation and modification reactions used to cross-link proteins or couple labels to proteins, such as biotin, enzymes, and fluorescent dyes, require certain conditions, including pH and chemical composition, for optimal conjugation. Many

The conjugation and modification reactions used to cross-link proteins or couple labels to proteins, such as biotin, enzymes, and fluorescent dyes, require certain conditions, including pH and chemical composition, for optimal conjugation. Many

Zymography is an electrophoretic technique, based on SDS-PAGE, that includes an enzyme substrate copolymerized with the polyacrylamide gel. Samples are prepared in Zymogram Sample Buffer without boiling to preserve the structure and activity of the

Zymography is an electrophoretic technique, based on SDS-PAGE, that includes an enzyme substrate copolymerized with the polyacrylamide gel. Samples are prepared in Zymogram Sample Buffer without boiling to preserve the structure and activity of the

Zymography is an electrophoretic technique, based on SDS-PAGE, that includes an enzyme substrate copolymerized with the polyacrylamide gel. Samples are prepared in Zymogram Sample Buffer without boiling to preserve the structure and activity of the

For Water Hardness, ASTM Formulation Formula: Mixture

For Water Hardness, ASTM Formulation Formula: Mixture