Crosslinking Reagents
Cayman Chemical Val-CIt-PAB-OH 250mg
A peptide linker molecule; cleaved by cathepsin B; has been used in the synthesis of ADCs containing KGP05 or MMAD, as well as α-galactosylceramide or folic acid conjugates that target peptide antigens to natural killer T cells or CRM1 inhibitors to cancer cells, respectively
Cell Signaling Technology Whitlow218 Linker F2G3S Rabbit mAb 20 ul
Whitlow218 Linker F2G3S Rabbit mAb 20 ul
eMolecules 79642-50-5 | DSG Crosslinker | ChemScene | MFCD00153597 | 326.261 | C13H14N2O8 | 97.000 | O=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 5g | 654745028
DSG Crosslinker | ChemScene | 79642-50-5 | MFCD00153597 | 326.261 | C13H14N2O8 | 97.000 | O=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 5g | 654745028
eMolecules 79642-50-5 | DSG Crosslinker | Ambeed | MFCD00153597 | 326.261 | C13H14N2O8 | 97.000 | O=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 1g | 570581003
DSG Crosslinker | Ambeed | 79642-50-5 | MFCD00153597 | 326.261 | C13H14N2O8 | 97.000 | O=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 1g | 570581003
Cayman Chemical Val-CIt-PAB-OH 25mg
A peptide linker molecule; cleaved by cathepsin B; has been used in the synthesis of ADCs containing KGP05 or MMAD, as well as α-galactosylceramide or folic acid conjugates that target peptide antigens to natural killer T cells or CRM1 inhibitors to cancer cells, respectively
Cayman Chemical Mc-Val-CIt-PABC-PNP 5mg
A peptide linker molecule; used in the synthesis of antibody-drug conjugates
Cayman Chemical Mc-Val-CIt-PABC-PNP 1mg
A peptide linker molecule; used in the synthesis of antibody-drug conjugates
eMolecules 79642-50-5 | DSG Crosslinker | Ambeed | MFCD00153597 | 326.261 | C13H14N2O8 | 97.000 | O=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 250mg | 534086561
DSG Crosslinker | Ambeed | 79642-50-5 | MFCD00153597 | 326.261 | C13H14N2O8 | 97.000 | O=C(CCCC(=O)ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 250mg | 534086561
Medchemexpress LLC DSG Crosslinker 5mg | 79642-50-5 | 326.26 g·mol^-1 | C13H14N2O8 | 5 MG
DSG Crosslinker (disuccinimidyl glutarate) is a homobifunctional N-hydroxysuccinimide (NHS) ester crosslinker that couples primary amines via a glutarate spacer. It is used for protein crosslinking, bioconjugation, surface immobilization, and as a linker in antibody-drug conjugate (ADC) research. Supplied for research use only.
- Reacts with primary amines to form stable amide bonds.
- Homobifunctional NHS-ester enabling amine-to-amine crosslinking.
- Membrane-permeable, suitable for intracellular crosslinking.
- Applicable to ADC synthesis, protein conjugation, and surface immobilization.
- Typically supplied at ~98.0% purity in small research pack sizes.
Cayman Chemical Val-CIt-PAB-OH 100mg
A peptide linker molecule; cleaved by cathepsin B; has been used in the synthesis of ADCs containing KGP05 or MMAD, as well as α-galactosylceramide or folic acid conjugates that target peptide antigens to natural killer T cells or CRM1 inhibitors to cancer cells, respectively