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    Results for Click Chemistry ( 905 )

      • Ref: BP-24335
        Sizes: 1 G, 500 MG, 250 MG

        Val-Cit is a cleavable ADC linker used in antibody drug conjugate. The Val-Cit linker was designed to be cleaved by cathepsin B. As this enzyme is only present in the lysosome, the ADC payload will be released only in the cell. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24363
        Sizes: 100 MG, 500 MG, 250 MG

        MC (C5)-Val-Cit is a cleavable ADC linker. The Val-Cit was designed to be cleaved specifically by Cathepsin B. MC is reactive with thiol moiety Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24365
        Sizes: 1 G, 100 MG, 500 MG

        t-butyl-octadecanedioate-NHS ester has a t-butyl ester group and an NHS ester moiety. The t-butyl group can be deprotected under acidic conditions. NHS ester can react specifically and efficiently with primary amines such as the side chain of lysine residues or aminosilane-coated surfaces at neutral or slightly basic condition to form a covalent bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24383
        Sizes: 1 G, 2 G

        Fmoc-Gly-Gly-Gly-OH Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24405
        Sizes: 100 MG, 500 MG, 250 MG

        6-(tert-Butoxy)-6-oxohexanoic NHS ester has a t-butyl ester group and an NHS ester moiety. The t-butyl group can be deprotected under acidic conditions. NHS ester can react specifically and efficiently with primary amines such as the side chain of lysine residues or aminosilane-coated surfaces at neutral or slightly basic condition to form a covalent bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24406
        Sizes: 100 MG, 500 MG, 250 MG

        10-(tert-Butoxy)-10-oxodecanoic NHS ester has a t-butyl ester group and an NHS ester moiety. The t-butyl group can be deprotected under acidic conditions. NHS ester can react specifically and efficiently with primary amines such as the side chain of lysine residues or aminosilane-coated surfaces at neutral or slightly basic condition to form a covalent bond. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24414
        Sizes: 5 MG, 25 MG, 10 MG

        Amino-PEG4-Val-Cit-PAB-MMAE is a cleavable ADC linker featuring a primary amine, a hydrophilic PEG spacer, and a Val-Cit-PAB dipeptide ligated to an MMAE payload. Primary amines readily form amides with carboxylic acids in the presence of activator reagents such as HATU or EDC, while the Val-Cit-PAB motif is an enzyme-cleavable linker. This linker efficiently releases the toxin, MMAE, to target cells to cause cellular apoptosis.

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      • Ref: BP-24415
        Sizes: 5 MG, 25 MG, 10 MG

        endo-BCN-PEG4-Val-Cit-PAB-MMAE is a peptide ADC linker with a BCN group. The hydrophilic PEG4 spacer increases solubility in aqueous media. The BCN group can react with azide-tagged biomolecules. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-24431
        Sizes: 1 MG, 5 MG, 10 MG

        Azido-PEG4-Val-Cit-PAB-MMAE is a precursor of antibody drug conjugate. It contains an azido-PEG4 spacer, a protease-sensitive Val-Cit dipeptide, a PABC linker and a MMAE payload.Azido enable click chemistry with alkyne-bearing moiety Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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