Solution hydrochlorure de phosphine Tris (2 carboxyethyl),0,5 m, pH 7,0 (solution aqueuse ; le pH a été ajusté à l'aide d'hydroxyde d'ammonium)

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Tris (2-carboxyethyl) phosphine (TCEP) has also been used:to cleave cysteine residues in a synthetic peptidein reduction buffer for RNA Sequential Probing of Targets (SPOTs) imagingfor the reduction of oligonucleotidesas reducing agent during mitochondrial isolation

Tris (2-carboxyethyl) phosphine (TCEP) can be used in several downstream applications including SDS-PAGE, mass spectrometry, labeling with cysteine specific tags, and modification of cysteine containing compounds. It prevents oxidation of protein samples, which makes it a useful buffer component as it helps to preserve enzymatic activity. It has been used in the reduction and measurement of glutathione.

Biochem/physiol Actions

As a non-mercaptan reducing agent, it avoids the toxicity inherent in thiol-containing compounds. It is capable of disrupting the botulinum neurotoxin B heavy-chain/light-chain complex that is held together by a single disulfide bond, and that is responsible for endocytosis, and ultimately the toxicity, of the toxin. Since disulfide-coupled subunits are characteristic of many toxins (e.g., ricin, snake venom, and all BoNT serotypes), it may be useful as a rescue prophylactic in cases of toxin administration.

Tris(2-carboxyethyl)phosphine hydrochloride solution reduces the disulfide bonds and leaves other functional groups intact in proteins.

General description

Tris (2-carboxyethyl) phosphine (TCEP) is very effective in cleaving disulfide bonds in aqueous solution. It dissolves in water and is odorless, unlike other trialkylphosphines (tributylphosphine). It is also less toxic than 2-mercaptoethanol. These advantages make it better than the other reducing agents.

It belongs to the trialkylphosphine class.

Packaging

10×1 mL in ampule