Sodium thiosulfate or thiosulfate or thiosulphate

A highly reactive, thiol-specific spin-label analog. It is a specific conformational probe of the thiol site structure due to its minimal rotational freedom and distance from the covalent disulfide linkage to the macromolecule under study.

An analog of &beta-D-glucose in which sulfur replaces the hydroxyl group at the one position, allowing diverse chemical reactions, including click chemistry and polymerization can be labeled with technetium-99m for analytical and diagnostic

An analog of &beta-D-glucose in which sulfur replaces the hydroxyl group at the one position, allowing diverse chemical reactions, including click chemistry and polymerization can be labeled with technetium-99m for analytical and diagnostic

An analog of &beta-D-glucose in which sulfur replaces the hydroxyl group at the one position, allowing diverse chemical reactions, including click chemistry and polymerization can be labeled with technetium-99m for analytical and diagnostic

Biochem/physiol Actions More potent than NMMA as an inhibitor of inducible nitric oxide synthetase (iNOS).

Biochem/physiol Actions More potent than NMMA as an inhibitor of inducible nitric oxide synthetase (iNOS).

2-THIOPHENESULFONIC ACID SODIUM SALT MONOHYDRATE

Application 3,3&#8242-Thiodipropanol was used in the determination of thiodiglycol in groundwater by a highly sensitive analytical method .

Thiol-specific, highly reactive cross-linking label for spin.

Application：Competitive inhibitor of T4 RNA ligase；Kinetic parameters with thiopurine methyltransferase；Interaction with (sodium-potassium ion)-dependent ATPase.

Note: Unstable at room temperature. Prepared enzymatically.

Alternative Thioglycollate Medium is formulated as described in the N.I.