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    Results for Click Chemistry ( 984 )

      • Ref: BP-23285
        Sizes: 100 MG, 500 MG, 250 MG
        From: €1,470.00

        Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB PAB is a unique peptide cleavable ADC linker for antibody-drug-conjugation, PEG spacer increases the aqueous solubility. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-23292
        Sizes: 1 G, 500 MG, 250 MG, 5 G
        From: €225.00

        MC-Val-Cit-PAB-PNP is a cleavable ADC linker which contains a maleimide, a valine-citrulline (Val-Cit dipeptide, and a para-nitrophenyl (PNP) group. Maleimide is a thiol-specific covalent linker which is used to label cysteine residues in proteins while the PNP carbonate acts as a highly activated leaving group which may be used to react with amines. Val-Cit linkers are cleaved by Cathepsin B.

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      • Ref: BP-23297
        Sizes: 100 MG, 50 MG, 250 MG
        From: €1,170.00

        Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP is a peptide reagent for ADC conjugation, it possesses a cleavable peptide sequence. PEG spacer increases the aqueous solubility. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-23328
        Sizes: 25 MG, 100 MG, 50 MG
        From: €675.00

        Fmoc-PEG4-Ala-Ala-Asn-PAB is a unique peptide cleavable peptide linker, PEG spacer increases the aqueous solubility. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-23329
        Sizes: 100 MG, 50 MG, 250 MG
        From: €975.00

        Azido-PEG5-Ala-Ala-Asn-PAB PAB is a unique peptide cleavable ADC linker for antibody-drug-conjugation, Azido group is very reactive toward DBCO, BCN or other Alkyne groups, called click chemistry. PEG spacer increases the aqueous solubility. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-23334
        Sizes: 100 MG, 50 MG, 250 MG
        From: €570.00

        Active-Mono-Sulfone-PEG8-acid is a PEG linker with a sulfone and acid end group. The sulfone group can be conjugated with thiol groups of proteins. The terminal carboxylic acid can react with primary amines in the presence of activators such as EDC and HATU to from stable amide bonds. The hydrophilic PEG chain increases the water solubility of the compound in aqueous media. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

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      • Ref: BP-23342
        Sizes: 100 MG, 50 MG, 250 MG
        From: €1,035.00

        Bis-sulfone-PEG12-NHS Ester is a bis-alkylating labeling reagent that is selective for the cysteine sulfur atoms from a native disulfide. These reagents undergo bis-alkylation to conjugate both thiols derived from the two cysteine residues of a reduced native disulfide bond such as the interchain disulfide bonds of an antibody. The reaction results in covalent rebridging of the disulfide bond via a three carbon bridge leaving the protein structurally intact. 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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      • Ref: BP-23343
        Sizes: 100 MG, 500 MG, 250 MG
        From: €525.00

        Bis-sulfone-PEG4-NHS Ester is a bis-alkylating labeling reagent that is selective for the cysteine sulfur atoms from a native disulfide. These reagents undergo bis-alkylation to conjugate both thiols derived from the two cysteine residues of a reduced native disulfide bond such as the interchain disulfide bonds of an antibody. The reaction results in covalent rebridging of the disulfide bond via a three carbon bridge leaving the protein structurally intact. 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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      • Ref: BP-23344
        Sizes: 1 G, 100 MG, 500 MG
        From: €420.00

        Bis-sulfone NHS Ester is a bis-alkylating labeling reagent that is selective for the cysteine sulfur atoms from a native disulfide. These reagents undergo bis-alkylation to conjugate both thiols derived from the two cysteine residues of a reduced native disulfide bond such as the interchain disulfide bonds of an antibody. The reaction results in covalent rebridging of the disulfide bond via a three carbon bridge leaving the protein structurally intact. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

        Product detail