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Catalog | Product Name | CAS Number |
---|---|---|
BADC-01232 | Biotin-PEG3-aldehyde | 889443-90-7 |
Biotin-PEG3-aldehyde is an aldehyde-functionalized ADC linker with biotin affinity, facilitating rapid site-specific antibody conjugation, purification, and improved targeting in antibody-drug conjugate workflows. | Inquiry | |
BADC-01233 | Biotin-PEG3-SS-azide | 2866429-93-6 |
Biotin-PEG3-SS-azide is a cleavable ADC linker ideal for biotin-based conjugation in antibody-drug conjugates. Its disulfide bond ensures redox-sensitive drug release, and the PEG spacer enhances solubility and stability. Perfect for bioconjugation, click chemistry, and targeted cancer therapy. | Inquiry | |
BADC-01234 | Bocaminooxyacetamide-PEG2-Azido | |
Bocaminooxyacetamide-PEG2-Azido is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
BADC-01235 | Bocaminooxyacetamide-PEG3-alkyne | |
Bocaminooxyacetamide-PEG3-alkyne is a cleavable ADC linker with aminooxy and alkyne groups for oxime ligation and click chemistry, supporting versatile bioconjugation in antibody-drug conjugates. | Inquiry | |
BADC-01236 | Boc-amino-PEG3-SS-acid | |
Boc-amino-PEG3-SS-acid is a PEGylated cleavable ADC linker with Boc-protected amine and acid groups, facilitating antibody conjugation and controlled drug release via disulfide cleavage. | Inquiry | |
BADC-01237 | Boc-amino-PEG3-SSPy | |
Boc-amino-PEG3-SSPy is a cleavable, Boc-protected PEG linker containing disulfide and pyridyl disulfide groups, designed for redox-sensitive drug release in antibody-drug conjugates. | Inquiry | |
BADC-01238 | Boc-Gly-Gly-Phe-Gly-OH TFA | |
Boc-Gly-Gly-Phe-Gly-OH TFA, a self-assembly of N- and C-protected tetrapeptide, is a protease cleavable linker used for the antibody-drug conjugate (ADC). | Inquiry | |
BADC-01239 | Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA | |
Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA is a multifunctional ADC linker with cleavable Val-Cit-PAB structure, DBCO click handle, and protected amine. It supports sequential, bioorthogonal assembly of complex antibody-drug conjugates with high selectivity and stability. | Inquiry | |
BADC-01241 | DBCO-(PEG2-Val-Cit-PAB)2 | |
DBCO-(PEG2-Val-Cit-PAB)₂ is a dimeric ADC linker designed for dual payload delivery. Its DBCO moiety allows copper-free click conjugation, while the cleavable Val-Cit-PAB linker ensures controlled intracellular release, enhancing ADC potency and versatility. | Inquiry | |
BADC-01242 | DBCO-NHCO-S-S-NHS ester | |
DBCO-NHCO-S-S-NHS ester is a cleavable ADC linker integrating DBCO click chemistry and NHS ester for efficient antibody conjugation with disulfide bonds for triggered drug release. | Inquiry | |
BADC-01244 | DBCO-PEG3-propionic EVCit-PAB | |
DBCO-PEG3-propionic EVCit-PAB is a PEGylated ADC linker with DBCO and enzymatically cleavable EVCit-PAB peptide, optimized for stable antibody conjugation and controlled payload release in ADC development. | Inquiry | |
BADC-01245 | DBCO-PEG3-SS-NHS ester | |
DBCO-PEG3-SS-NHS ester is a cleavable PEGylated ADC linker featuring DBCO for click chemistry and NHS ester for amine conjugation, providing efficient and stable antibody-drug conjugate assembly. | Inquiry | |
BADC-01247 | DBCO-PEG4-acetic-Val-Cit-PAB | |
DBCO-PEG4-acetic-Val-Cit-PAB is a PEGylated ADC linker with DBCO for click chemistry and valine-citrulline for enzymatic cleavage, facilitating efficient and stable antibody-drug conjugate synthesis. | Inquiry | |
BADC-01249 | DBCO-PEG4-HyNic | |
DBCO-PEG4-HyNic is a dual-reactive ADC linker with DBCO for SPAAC click and HyNic for oxime ligation, enabling stable, site-specific payload conjugation in antibody-drug conjugates. | Inquiry | |
BADC-01250 | DBCO-PEG4-Propionic-Val-Cit-PAB | |
DBCO-PEG4-Propionic-Val-Cit-PAB features propionic acid modification with DBCO and valine-citrulline cleavable peptide, enhancing conjugation flexibility and controlled drug release in ADCs. | Inquiry | |
BADC-01251 | DBCO-PEG4-SS-TCO | |
DBCO-PEG4-SS-TCO is a cleavable ADC linker featuring DBCO and trans-cyclooctene moieties with a disulfide bond, enabling dual bioorthogonal conjugation and redox-triggered drug release in ADCs. | Inquiry | |
BADC-01252 | DBCO-SS-aldehyde | |
DBCO-SS-aldehyde is a cleavable ADC linker containing DBCO for strain-promoted click chemistry and aldehyde for oxime ligation, supporting versatile and stable antibody-drug conjugate synthesis. | Inquiry | |
BADC-01253 | DBCO-SS-amine | |
DBCO-SS-amine is a bifunctional cleavable ADC linker with DBCO and amine groups linked by a disulfide bond, enabling site-specific click chemistry and stable payload attachment. | Inquiry | |
BADC-01254 | DBCO-SS-PEG4-Biotin | |
DBCO-SS-PEG4-Biotin is a cleavable biotinylated ADC linker featuring DBCO for SPAAC and disulfide for intracellular payload release, facilitating affinity purification and targeted drug delivery. | Inquiry | |
BADC-01255 | DBCO-Val-Cit-OH | |
DBCO-Val-Cit-OH is a click chemistry-compatible ADC linker with valine-citrulline cleavable dipeptide for enzyme-triggered release, improving targeted payload delivery in antibody-drug conjugates. | Inquiry |