Hai cercato: Isopropyl+cyclohexanecarboxylate

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SMCC (N-Succinimidyl 4-(N-Maleimidomethyl)cyclohexanecarboxylate), Pierce™

Codice catalogo: (PIER22360)

Fornitore: Thermo Fisher Scientific

Codice articolo fornitore: 22360

Codice articolo locale: PIER22360

Descrizione: Thermo Scientific Pierce SMCC is a hetero-bifunctional crosslinker that contain N-hydroxysuccinimide (NHS) ester and maleimide groups that allow covalent conjugation of amine- and sulfhydryl-containing molecules. NHS esters react with primary amines at pH 7–9 to form amide bonds, while maleimides react with sulfhydryl groups at pH 6.5–7.5 to form stable thioether bonds. In aqueous solutions, NHS ester hydrolytic degradation is a competing reaction whose rate increases with pH. The maleimide group is more stable than the NHS-ester group, but will slowly hydrolyze and lose its reaction specificity for sulfhydryls at pH values > 7.5. For these reasons, conjugations with these crosslinkers are usually performed at pH 7.2–7.5, with the NHS ester (amine-targeted) reacted before or simultaneous with the maleimide (sulfhydryl-targeted) reaction.

UOM: 1 * 50 mg

MSDS Certificati Promo

Non disponibile confezione

SMCC (N-Succinimidyl 4-(N-Maleimidomethyl)cyclohexanecarboxylate) ≥85%

Fornitore: AAT BIOQUEST

Descrizione: SMCC is a non-cleavable and membrane permeable crosslinker with a spacer arm of 8.3 Å. It contains an amine-reactive succinimidyl ester (SE) and a sulfhydryl-reactive maleimide group. NHS esters react with primary amines at pH 7 to 9 to form stable amide bonds. Maleimides react with sulfhydryl groups at pH 6.5 to 7.5 to form stable thioether bonds. The SE group of SMCC is reacted with lysine residues on the carrier protein, converting them to reactive maleimides. SMCC is a reagent that is widely used for generating stable maleimide-activated carrier proteins that can spontaneously react with sulfhydryls. Alternatively these relatively stable maleimide-activated intermediates may be lyophilized and stored for later conjugation to a hapten.

Isopropyl myristate per sintesi, Sigma-Aldrich®

Fornitore: Merck

Descrizione: Isopropyl myristate per sintesi, Sigma-Aldrich®

MSDS Certificati

5-Isopropyl-2-methylphenol, Sigma-Aldrich®

Fornitore: Merck

Descrizione: 5-Isopropyl-2-methylphenol, Sigma-Aldrich®

MSDS

Isopropyl 2-bromo-2-methylpropionate per sintesi, Sigma-Aldrich®

Fornitore: Merck

Descrizione: Isopropyl 2-bromo-2-methylpropionate per sintesi, Sigma-Aldrich®

MSDS

4-Chloro-2-isopropyl-5-methylphenol

Codice catalogo: (8.20345.0050)

Fornitore: Merck

Codice articolo fornitore: 8.20345.0050

Codice articolo locale: MERC8.20345.0050

Descrizione: 4-Chloro-2-isopropyl-5-methylphenol

UOM: 1 * 25 g

MSDS Promo

Non disponibile confezione

2,5-Dibromo-6-isopropyl-3-methyl-1,4-benzoquinone, Sigma-Aldrich®

Codice catalogo: (271993-250MG)

Fornitore: SIGMA ALDRICH MICROSCOPY

Codice articolo fornitore: 271993-250MG

Codice articolo locale: SIAM271993-250MG

Descrizione: 2, 5-Dibromo-6-isopropyl-3-methyl-1, 4-benzoquinone has been used as a metabolic inhibitor of violaxanthin (V) cycle of Pelvetia canaliculata and is used as a photosynthetic electron transport chain (pETC) inhibitor.

UOM: 1 * 250 mg

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