Wyszukano: D-(-)-Luciferin+sodium+salt+monohydrate

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Fostriecin sodium salt (from Streptomyces pulveraceous subsp. fostreus) ≥98% (by HPLC)

Numer katalogowy: (ENZOALX380065C010)

Producent: ENZO LIFE SCIENCES

Opis: Antitumor antibiotic. Catalytic inhibitor of topoisomerase II. Strong protein phosphatase 2A (PP2A) inhibitor (IC50=3.2nM). Weak inhibitor for PP1 (IC50=131µM). No apparent effect on PP2B. The binding site for fostriecin on PP2A is different from that of okadaic acid.

j.m.: 1 * 10 µG

Wyprzedaż

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β-Cyclodextrin sulphobutyl ethers sodium salts (DS~10)

Producent: Apollo Scientific

Opis: β-Cyclodextrin sulphobutyl ethers sodium salts (DS~10)

Sodium-1-naphthalenesulphonate, (max. 2% H₂O) 99% (dry weight)

Producent: Thermo Fisher Scientific

Opis: Sodium-1-naphthalenesulphonate, (max. 2% H₂O) 99% (dry weight)

MSDS Certyfikaty

6-deoxy-6-((2-carboxyethyl)disulphide)-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin sodium salt

Numer katalogowy: (APOSBICY1064-1MG)

Producent: Apollo Scientific

Opis: 6-deoxy-6-((2-carboxyethyl)disulphide)-heptakis(6-deoxy-6-(2-carboxyethyl)thio)-gamma-cyclodextrin sodium salt

j.m.: 1 * 1 mg

Wyprzedaż

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siarczan dodecylu sodu ≥98%, GPR RECTAPUR®

Producent: VWR Chemicals

Opis: siarczan dodecylu sodu ≥98%, GPR RECTAPUR®

MSDS Certyfikaty

Sulpho-NHS (N-Hydroxysulphosuccinimide sodium salt)

Numer katalogowy: (BC97)

Producent: G-Biosciences

Opis: 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.

j.m.: 1 * 500 mg

Wyprzedaż

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MK-571 sodium salt ≥90% (by HPLC)

Producent: ENZO LIFE SCIENCES

Opis: A potent, selective, orally active leukotriene D₄ antagonist. Ki=2.1 nM for inhibition of [³H]-LTD₄ binding to human lung membranes. Competitively antagonizes contractions of guinea pig trachea and ileum and human trachea induced by LTD₄. Blocks LTD₄ and ascaris-induced bronchoconstriction in conscious squirrel monkeys.