U heeft gezocht op: Dichloroisocyanuric+acid+sodium+salt+monohydrate

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AMI-1 ≥98% (by 1H-NMR, HPLC)

Catalogus nummer: (ENZOALX270440M005)

Leverancier: ENZO LIFE SCIENCES

Omschrijving: PRMT inhibitor

UOM: 1 * 5 mg

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Diphenyliodonium-2-carboxylate monohydrate ≥98.0% (by HPLC, titration analysis)

Leverancier: TCI

Omschrijving: Diphenyliodonium-2-carboxylate monohydrate ≥98.0% (by HPLC, titration analysis)

Coomassie® brilliant blue R-250, Sigma-Aldrich®

Catalogus nummer: (1.12553.0025)

Leverancier: Merck

Omschrijving: Coomassie® brilliant blue R-250, Sigma-Aldrich®

UOM: 1 * 25 g

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Disodium naphthalene-1,5-disulphonate 98%

Leverancier: Apollo Scientific

Omschrijving: Disodium naphthalene-1,5-disulphonate 98%

Sulpho-NHS (N-Hydroxysulphosuccinimide sodium salt)

Catalogus nummer: (BC97)

Leverancier: G-Biosciences

Omschrijving: Sulpho-NHS reacts primarily with primary amines to convert carboxyl groups to amine reactive sulfo-NHS esters. It is ideal for cross-linking, chemical labelling and solid support immobilisation. It is used to generate amine reactive esters from carboxylate groups and is primarily used to increase the efficiency of the carbodiimide EDC cross-linking. EDC reactions do not require Sulpho-NHS; however, its presence greatly enhances cross-linking efficiency and allows for a two-step process. EDC reacts with a carboxylate group to form an active ester, which is subject to rapid hydrolysis in aqueous buffers. The Sulfo-NHS increases the stability of the active intermediate and the resulting coupled product is identical to EDC reactions without sulpho-NHS.

UOM: 1 * 500 mg

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Ponceau S ≥85.0% (by total nitrogen basis) for biochemical research

Leverancier: TCI

Omschrijving: Ponceau S ≥85.0% (by total nitrogen basis) for biochemical research

Dinatriumdisulfiet ≥97%, GPR RECTAPUR®

Leverancier: VWR Chemicals

Omschrijving: Dinatriumdisulfiet ≥97%, GPR RECTAPUR®

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Sodium 4-phenylbutyrate ≥98% (by UHPLC)

Catalogus nummer: (ENZOBMLEI3200001)

Leverancier: ENZO LIFE SCIENCES

Omschrijving: Weak histone deacetylase (HDAC) inhibitor. Induces differentiation, growth arrest and apoptosis in a number of cell lines. Protects against cerebral ischemic injury and displays neuroprotective effect in a mouse model of Huntington’s disease. Anti-neoplastic agent and transcriptional regulator. Also acts as an inducer of tumor cytostasis and differentiation. Shows chemical chaperone activity.

UOM: 1 * 1 g

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