MPBH(Protein Crosslinker heterobifunctional) CL216 4-(N-Maleimidophenyl)butyric acid hydrazide hydrochloridef.w.: 309.7 daltons |
MPBH is a long, maleimide-and-hydrazide crosslinker for conjugating sulfhydryls (cysteines) to carbonyls (aldehyde or ketones, such as those formed by oxidation of glycoprotein carbohydrates).
Spacer arm 17.9 angstroms. Heterobifunctional crosslinker. Carbohydrate selective and sulfhydyl reactive. MPBH has an oxidized carbohydrate specific hydrazide, a sulfhydryl reactive group and a spacer arm to accommodate a wide range of molecular coupling manipulations.
1.Chamow, S.M., Kogan, T.P., Peers, D.H., Hastings, R.C., Byrn, R.A. and Askenaszi, A. (1992). Conjugation of soluble CD4 without loss of biological activity via a novel carbohydrate-directed crosslinking reagent. J. Biol. Chem. 267(22), 15916-15922.
• Has an oxidized carbohydrate specific hydrazide, a sulfhydryl reactive group and spacer arms to accommodate a wide range of molecular coupling demands • -SH specific group is a maleimide that yields a thioether linkage upon coupling • Stable in DMSO • Reactive groups: hydrazide and maleimide • Reactive towards: carbohydrate and sulfhydryl groups • Use with EDC for reactivity toward carboxyl groups Product Details: