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Supplier: Merck
Description: Sulpholane 99,0 zS, Sigma-Aldrich®

SDS

Catalog Number: (456063-25G)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: 1-Amino-4-bromoanthraquinone-2-sulphonic acid sodium salt, Sigma-Aldrich®
UOM: 1 * 25 g


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Supplier: SIGMA ALDRICH MICROSCOPY
Description: 8-Anilino-1-naphthalenesulphonic acid, Sigma-Aldrich®

Catalog Number: (55370-100G)
Supplier: Merck
Description: Reagent for spectrophotometric det. of Fe(III)
UOM: 1 * 100 g


Catalog Number: (10322.)
Supplier: Merck
Description: Amberlite IR 120-H, gel type acidic cation exchange resin is of sulfonated polystyrene type having tremendous stability. It is an efficient heterogeneous catalyst for organic reactions.
UOM: 1 * 500 g

Supplier: Avantor
Description: 1-Pentanesulphonic acid sodium salt 98 Ionpair, J.T.Baker®
Catalog Number: (210684-25G)
Supplier: SIGMA ALDRICH MICROSCOPY
Description: Acid Blue 25, Dye content 45 %
UOM: 1 * 25 g


Supplier: Thermo Fisher Scientific
Description: Phenyl vinyl sulphone 99
Supplier: Merck
Description: Sulphanilic acid ACS, Reag. Ph. Eur. analytical reagent, Supelco®

SDS

Catalog Number: (75768-25MG)
Supplier: Merck
Description: Congo red, Supelco®
UOM: 1 * 25 mg


Supplier: Merck
Description: 1-Heptanesulphonic acid sodium salt, LiChropur™ for ion pair chromatography, Supelco®
Catalog Number: (APOSOR350345-100G)
Supplier: Apollo Scientific
Description: Sodium-6,7-dihydroxynaphthalene-2-sulphonate
UOM: 1 * 100 g


Supplier: Merck
Description: Sodium-1-decanesulphonate, Supelco®
Supplier: Thermo Fisher Scientific
Description: Bis(4-chlorophenyl)sulphone 99
Supplier: Merck
Description: Methyl toluene-4-sulphonate zS, Sigma-Aldrich®

SDS

Catalog Number: (ENZOBMLZW91700500)
Supplier: ENZO LIFE SCIENCES
Description: Inhibits the trypsin-like, chymotrypsin-like and caspase-like (PGPH) activity in isolated proteasomes and living cells by covalent modification of the amino-terminal threonine of the catalytically active beta subunits. The vinyl sulfone acts as a Michael acceptor for soft nucleophiles such as thiols, leading to the formation of a covalent bond, while being resistant to attack by free thiols, which can cause inactivation of other classes of protease inhibitors.
UOM: 1 * 500 µG

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