Learn More
Medchemexpress LLC Dbco-peg2-val-cit-pab-mmae | 2845934-59-8 | MFCD35133151 | 99.3% | 1569.92 | C84H120N12O17 | 50 MG

Supplier: Medchemexpress LLC HY17228750MG
DBCO-PEG2-Val-Cit-PAB-MMAE is a cleavable antibody-drug conjugate (ADC) linker that combines a DBCO strain-promoted alkyne handle, a short PEG2 spacer, a protease-cleavable Val-Cit dipeptide, a para-aminobenzyl (PAB) self-immolative spacer, and an MMAE cytotoxic payload. It is intended for research use in ADC synthesis and click-chemistry conjugation.
- cleavable Val-Cit dipeptide for protease-triggered payload release.
- dbco click handle enables copper-free SPAAC conjugation to azides.
- peg2 spacer provides linker flexibility and solubility.
- para-aminobenzyl (PAB) self-immolative spacer facilitates payload release.
- includes a potent MMAE payload for cytotoxic activity in ADC constructs.
- supplied as a 50 mg package for laboratory research use.
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.