Cat#: CLP-0029
3-Maleimidobenzoic acid N-hydroxysuccinimide ester
Synonyms (s): MBS
Empirical Formula (Hill Notation): C15H10N2O6
Size: 25 mg; 100 mg
Product Introduction
| Molecular Weight | 314.25 |
| CAS Number | 58626-38-3 |
| MDL Number | MFCD00005514 |
| PubChem Substance ID | 24896768 |
| Form | Liquid |
| Reaction Suitability | Reagent type: Cross-linking reagent |
| Smiles String | O=C1CCC(N1OC(C2=CC=CC(N3C(C=CC3=O)=O)=C2)=O)=O |
| InChI | 1S/C15H10N2O6/c18-11-4-5-12(19)16(11)10-3-1-2-9(8-10)15(22)23-17-13(20)6-7-14(17)21/h1-5,8H,6-7H2 |
| InChI key | LLXVXPPXELIDGQ-UHFFFAOYSA-N |
| Storage Temp. | -20 °C |
Application
3-Maleimidobenzoic acid N-hydroxysuccinimide ester (MBS) has been used as a protein cross-linker. It has been used for the stabilization of actin filaments in plant tissue samples.
3-Maleimidobenzoic acid N-hydroxysuccinimide ester has been used:in the fixation of pollen in Arabidopisas a component of Murashige and Skoog (MS) medium to stabilize F-actin in Eucalyptus root hairsin the fixation of F-actin labelled pollen tubes of Lilium davidii
Heterobifunctional crosslinking reagent reactive toward primary amine and sulfhydryl. Typically, coupled initially to molecules containing primary amines by amide bonds buffered at pH 7.0, followed by coupling to compounds containing sulfhydryl by thioether at same pH. Useful for preparation of enzyme immunoconjugates and hapten carrier molecule conjugates.
Safety Information
| Storage Class Code | 11 - Combustible Solids |
| WGK | WGK 3 |
For research use only. Not for clinical use.
