Cas No.: 28537-70-4
PRODUCT INFORMATION
Description
This is a homobifunctional, sulfhydryl-reactive crosslinker. It consists of two maleimide groups separated by a short, 4-carbon (C4) aliphatic spacer. Maleimide groups react specifically with thiols (cysteines) at neutral pH (6.5-7.5) to form stable, non-cleavable thioether bonds. BMB is primarily used to crosslink two different thiol-containing molecules (e.g., two peptides) or to induce intramolecular crosslinks between two cysteine residues within the same protein. This can be used to study or stabilize protein tertiary/quaternary structure.
Molecular Weight
248.24
Purity
>98.0%
Formula
C₁₂H₁₂N₂O₄
Product Type
Homobifunctional Crosslinkers
Group 1
Maleimide
Group 2
Maleimide
Form (20 deg.C)
Solid
Storage Condition
Store under inert gas, <0°C
Molecular Structure
For Research Use Only | Not For Clinical Use
Related products
- N-(tert-Butoxycarbonyl)-2,2'-(ethylenedioxy)diethylamine (CAT#: OLY-1023-YS145)
- Dithiobis(succinimidyl propionate) (DSP) Homobifunctional Crosslinker (CAT#: OLY-1023-YS141)
- m-PEG12-maleimide (CAT#: OLY-1023-YS243)
- 1-[3-(Dimethylamino)propyl]-3-ethylcarbodiimide Methiodide Zero-Length Crosslinker (CAT#: OLY-1023-YS285)
- N-([ε-Maleimidocaproyloxy)sulfosuccinimide Ester (Sulfo-EMCS) (CAT#: OLY-1023-YS88)
- Biotin-PEG4-alkyne (CAT#: OLY-1023-YS202)
- N,N'-Ethylenedimaleimide (CAT#: OLY-1023-YS137)
- β-Alanine tert-butyl Ester Hydrochloride Heterobifunctional Crosslinker (CAT#: OLY-1023-YS112)
Online Inquiry
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
