| Cat.No. | Name | Information |
|---|---|---|
| M10413 | Boc-Val-Cit-PAB | Boc-Val-Cit-PAB is a cleavable ADC linker used in making antibody-drug conjugates (ADCs). |
| M10412 | Val-cit-PAB-OH | Val-cit-PAB-OH is a cathepsin cleavable ADC peptide linker for making MC-Val-Cit-PAB, which is also known as MC-Val-Cit-PAB-OH. |
| M10411 | Fmoc-Val-Cit-PAB-PNP | Fmoc-Val-Cit-PAB-PNP is a cleavable peptide ADC linker which used in the synthesis of antibody-drug conjugates (ADCs). |
| M10410 | Fmoc-Val-Cit-PAB | Fmoc-Val-Cit-PAB-OH is a cleavable useful heterobifunational linker for making Antibody-Drug-Conjugates (ADC). |
| M10409 | Mc-Val-Cit-PAB | Mc-Val-Cit-PAB is a peptide linker molecule used in the synthesis of antibody-drug conjugates (ADCs). |
| M10401 | SPDP Crosslinker | SPDP crosslinker, or SPDP NHS ester, is a cleavable, water insoluble, amino and thiol (sulfhydryl) reactive heterobifunctional protein crosslinker. *The compound is unstable in solutions, freshly prepared is recommended |
| M10092 | Sulfo-NHS | Sulfo-NHS is a peptide condensing agent, can form a stable active ester intermediate, used to prepare hydrophilic active ester, for example as a protein cross-linking agent. N-Hydroxysulfosuccinimide (sodium) is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
| M6213 | 6-Maleimidohexanoic acid N-hydroxysuccinimide ester | 6-Maleimidohexanoic acid N-hydroxysuccinimide ester(ECMS) is a useful protective group in antibody drug conjugates. |
| M59400 | m-PEG8-Amine | m-PEG8-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
| M59399 | m-PEG4-Amine | m-PEG4-Amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. |
| M59398 | N-Butanoyl-L-homoserine lactone | N-Butanoyl-L-homoserine lactone (C4-HSL) is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
| M59397 | AMAS | AMAS is a nonclaevable heterobifunctional crosslinker with NHS ester and maleimide groups that allows covalent conjugation of amine- and sulfhydryl-containing molecules. |
| M59396 | DBCO-PEG3-oxyamine | DBCO-PEG3-oxyamine is a non-cleavable 3 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
| M59395 | MC-Gly-Gly-Phe-Gly | MC-Gly-Gly-Phe-Gly is a cleavable ADC linker used for antibody-drug conjugates (ADCs). |
| M59394 | m-PEG7-Amine | m-PEG7-Amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. |
| M59393 | MC-Val-Ala-OH | MC-Val-Ala-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
| M59268 | N3-TEMPO | N3-TEMPO is a click chemistry reagent containing an azide group. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. |
| M59160 | Cy5.5 DBCO | Cy5.5 DBCO is a click chemistry reagent containing an cycloalkynes group. Cy5.5 DBCO is a linker of Cyanine5.5 fluorophore. DBCO group enables copper free biocompatible click chemistry with fast reaction kinetics and good stability. |
| M55732 | SPDB-sulfo | SPDB-sulfo is a glutathione cleavable ADC linker used for the antibody-drug conjugate (ADCs) . |
| M55731 | Tr-PEG5-OH | Tr-PEG5-OH is a non-cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.
