Results for Lipids & Polymers ( 10156 )
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m-PEG3-amine is a PEG reagent containing an amino group (NH2). The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The hydrophilic PEG spacer increases solubility in aqueous media. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
- From: €405.00
m-PEG3-S-Acetyl is a PEG linker with a sulfur-acetyl end group. The sulfur acetyl group can be deprotected to generate thiol groups. After the formation of the thiol group, it is able to react with maleimides, disulfides, haloacteamides and other thiols. The hydrophilic PEG linker increases the solubility of the compound in aqueous media. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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m-PEG3-NHS ester is a PEG linker containing an NHS ester. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. The hydrophilic PEG spacer increases solubility in aqueous media. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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m-PEG3-acid is a PEG linker containing a terminal carboxylic acid. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The hydrophilic PEG spacer increases solubility in aqueous media. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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Bromoacetamido-PEG2-acid is a PEG linker containing a bromide group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.
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Mal-C6-amine TFA salt contains maleimide and amine end groups. Maleimides are react with thiol groups and form thiolester bonds between pH 6.5 to 7.5. The primary amine can react with carboxylic acids, activated NHS esters and other carbonyl compounds. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.