KMUH N-(kappa-Maleimidoundecanoic acid) hydrazide

Protein Crosslinker heterobifunctional

Catalog #CL224
Formula Weightf.w.: 295.4 daltons

KMUH 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).

Pricing & Ordering

Quantity Price Action
50mgm + $103.50
100mgm + $195.50


Spacer arm 19.0 angstroms. Heterobifunctional crosslinker. Sulfhydryl reactive and carbonyl reactive. Long non-cleavable aliphatic spacer arm. Hydrazide group covalently couples to oxidized carbohydrate residues in glycoproteins and other glycoconjugates.

1. Trail, P.A., et al. (1993). Cure of xenografted human carcinomas by BR96-doxorubicin immunoconjugates. Science 261, 212-215.

  • Sulfhydryl-reactive and carbonyl-reactive heterobifunctional crosslinking agent
  • Long, non-cleavable, aliphatic cross-bridge
  • Hydrazide group covalently couples to oxidized carbohydrate residues in glycoproteins and other glycoconjugates
  • Maleimide reacts with -SH groups at pH 6.5-7.5, forming stable thioether linkages
  • Reactive groups: maleimide and hydrazide
  • Reactive toward: sulfhydryl and carbonyl (aldehyde)/carboxyl groups

EMCS

N-(epsilon-Maleimidocaproyloxy)succinimide

CAS 55750-63-5

GMBS

N-(gamma-Maleimidobutyryloxy)succinimide

CAS 80307-12-6

LC SMCC

Succinimidyl-4-(N-maleimidomethyl)-cyclohexane-1-carboxy(6-amidocaproate)

MBH

m-Maleimidobenzoic acid hydrazidehydrochloride

MBS

3-Maleimidobenzoyl-N-hydroxysuccinimide ester

CAS 58626-38-3

MCCH

4-(N-Maleimidomethyl)cyclohexane-1-carboxylic acid hydrazide hydrochloride