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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T18799 | Tetrazine-Ph-OPSS | Others | |
Tetrazine-Ph-OPSS is an ADC linker employed for synthesizing ADCs, or antibody-drug conjugates [1]. | |||
T18510 | OPSS-PEG36-acid | Others | |
OPSS-PEG36-acid is a 36-unit PEG linker amenable to cleavage, specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T16400 | OPSS-PEG8-COOH | Others | |
OPSS-PEG8-COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T17369 | Ald-Ph-amido-PEG23-OPSS | Others | |
Ald-Ph-amido-PEG23-OPSS is a cleavable 23-unit polyethylene glycol linker commonly employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T19780 | 2,2′-Dipyridyl disulfide | 2,2'-Dipyridyl disulfide,OPSS,Aldrithiol 2,Orthopyridyl disulfide | Others |
2,2′-Dipyridyl disulfide (Aldrithiol 2) is a useful reagent for the determination of sulfhydryl groups. It acts as a peptide coupling reagent and as an oxidizing agent. 2,2′-Dipyridyl disulfide (Aldrithiol 2) is also use... | |||
T18512 | OPSS-Val-Cit-PAB-PNP | Others | |
OPSS-Val-Cit-PAB-PNP is a cleavable linker employed in ADC (antibody-drug conjugates) synthesis [1]. | |||
T18511 | OPSS-Val-Cit-PAB-OH | Others | |
OPSS-Val-Cit-PAB-OH is an ADC linker utilized for the synthesis of antibody-drug conjugates (ADCs) [1]. | |||
T30477 | Bis-PEG5-thiol | ||
Bis-PEG5-thiol is a PEG derivative containing two thiol groups. The thiol groups react with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc. The hydrophilic PEG spacer increases so... | |||
T71953 | Thiol-PEG2-acid | ||
Thiol-PEG2-acid is a PEG derivative containing a thiol group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The thiol group reacts with maleimide, OPSS, vinylsulfone and... |