About 30 results found for searched term "Antibody-Drug Conjugates (ADCs)" (0.13 seconds)
Cat.No. | Name | Target |
---|---|---|
M9872 | BS3 (bis(sulfosuccinimidyl)suberate) | Drug-Linker Conjugates for ADC |
BS3 Crosslinker | ||
BS3 (bis(sulfosuccinimidyl)suberate) is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M10092 | Sulfo-NHS | ADC Linker |
N-hydroxysulfosuccinimide sodium | ||
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). | ||
M10199 | DSS Crosslinker (Disuccinimidyl suberate) | Drug-Linker Conjugates for ADC |
Disuccinimidyl suberate | ||
DSS Crosslinker (Disuccinimidyl suberate) is a non-cleavable, cell membrane permeable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M10409 | Mc-Val-Cit-PAB | ADC Linker |
MC-Val-Cit-PAB-OH | ||
Mc-Val-Cit-PAB is a peptide linker molecule used in the synthesis of antibody-drug conjugates (ADCs). | ||
M10411 | Fmoc-Val-Cit-PAB-PNP | ADC Linker |
Fmoc-Val-Cit-PAB-PNP is a cleavable peptide ADC linker which used in the synthesis of antibody-drug conjugates (ADCs). | ||
M10413 | Boc-Val-Cit-PAB | ADC Linker |
Boc-Val-Cit-PABA | ||
Boc-Val-Cit-PAB is a cleavable ADC linker used in making antibody-drug conjugates (ADCs). | ||
M10414 | Fmoc-3VVD-OH | ADC Linker |
Fmoc-3VVD-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M13453 | DBCO-NHS ester | ADC Linker |
DBCO-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M13454 | DSP Crosslinker | ADC Linker |
DSP Crosslinker is a cleavable ADC linker, used in the synthesis of antibody-drug conjugates (ADCs). | ||
M13455 | Fmoc-Phe-Lys(Boc)-PAB-PNP TFA | ADC Linker |
Fmoc-Phe-Lys(Boc)-PAB-PNP TFA is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M24766 | Pinatuzumab | Integrin |
Pinatuzumab is a CD22 monoclonal antibody. Pinatuzumab targets the cell-surface antigen CD22. Pinatuzumab can be used for synthesis of antibody drug conjugates (ADCs) to research several diseases including non-Hodgkin lymphoma (NHL). | ||
M24977 | Disitamab | EGFR/HER2 |
RC48-0 | ||
Disitamab (RC48-0) is a humanized monoclonal antibody targeting HER2. Disitamab can be used in the synthesis of antibody-drug conjugates (ADCs), Disitamab vedotin (Disitamab vedotin ). | ||
M25072 | Mipasetamab uzoptirine | TAM Receptor |
ADCT-601 | ||
Mipasetamab uzoptirine (ADCT-601) is an AXL-targeted antibody-drug conjugates (ADCs). Mipasetamab uzoptirine consists of a humanized anti-AXL antibody, a cleavable linker and the potent pyrrolobenzodiazepine (PBD) dimer cytotoxin SG3199. Mipasetamab uzoptirine can be used for the research of cancers. | ||
M25292 | Camidanlumab | IL Receptor/Related |
HuMax-TAC | ||
Camidanlumab (HuMax-TAC) is a CD25 monoclonal antibody. Camidanlumab targets the cell-surface antigen CD25, which is over-expressed on a variety of hematological tumors and shows limited expression on normal tissues. Camidanlumab can be used for synthesis of antibody drug conjugates (ADCs) to research several diseases including lymphoma and leukemia. | ||
M28617 | Hemiasterlin | Others |
(-)-Hemiasterlin; Milnamide B | ||
Hemiasterlin ((-)-Hemiasterlin) is an antimitotic marine natural product with potent anticancer effcts. Hemiasterlin can be used as a cytotoxic payload (ADC Cytotoxin) in antibody-drug conjugates (ADCs). | ||
M28881 | Mc-VC-PAB-SN38 | Drug-Linker Conjugates for ADC |
Mc-VC-PAB-SN38 consists a cleavable ADC linker (Mc-VC-PAB) and a DNA topoisomerase I inhibitor (SN38). Mc-VC-PAB-SN38 can be used in the synthesis of antibody-drug conjugates (ADCs). | ||
M29703 | Dazostinag | STING |
TAK-676 free base | ||
Dazostinag (TAK-676 free base) is an agonist of stimulator of interferon genes (STING) protein with antineoplastic activity. Dazostinag can serve as a playload to synthesis antibody-drug conjugates (ADCs). | ||
M30995 | DBCO-PEG4-acetic-Val-Cit-PAB | ADC Linker |
DBCO-PEG4-acetic-Val-Cit-PAB is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M38621 | H-Hyp-OMe hydrochloride | ADC Linker |
H-Hyp-OMe hydrochloride is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). H-Hyp-OMe hydrochloride is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. | ||
M38623 | Eicosanedioic acid | ADC Linker |
Eicosanedioic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Eicosanedioic acid is also a alkyl chain-based PROTAC linker that can be used in the synthesis | ||
M38624 | Boc-Hyp-OH | ADC Linker |
Boc-Hyp-OH is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Boc-Hyp-OH is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. | ||
M41003 | Mal-L-PA-NH-Boc | ADC Linker |
Mal-L-PA-NH-Boc is a noncleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M41004 | MC-VC-PAB-NH2 TFA | ADC Linker |
MC-VC-PAB-NH2 TFA is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M45209 | Maleimido-mono-amide-DOTA | ADC Linker |
Maleimide-DOTA | ||
Maleimido-mono-amide-DOTA is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M53849 | Mc-Gly-Gly-Phe-Gly-PAB-OH | ADC Linker |
Mc-Gly-Gly-Phe-Gly-PAB-OH (Mc-GGFG-PAB-OH) is a cleavable ADC linker used for antibody-drug conjugates (ADCs). | ||
M58138 | DBCO-Maleimide | ADC Linker |
DBCO-Maleimide is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). DBCO-Maleimide is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups. | ||
M55730 | DBCO-amine | ADC Linker |
DBCO-amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M55731 | Tr-PEG5-OH | ADC Linker |
Tr-PEG5-OH is a non-cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M55729 | Boc-Hyp-OMe | ADC Linker |
Boc-Hyp-OMe is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | ||
M55728 | Fmoc-Asp-NH2 | ADC Linker |
Fmoc-Asp-NH2 is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
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