Cas No.: 1585-90-6
PRODUCT INFORMATION
Description
This heterobifunctional crosslinker possesses a sulfhydryl-reactive maleimide group and a terminal primary hydroxyl group. The maleimide group reacts specifically with thiols (e.g., cysteine residues) at pH 6.5-7.5 to form a stable thioether bond. The terminal hydroxyl group is less nucleophilic than an amine but offers distinct conjugation possibilities. It is primarily used to prepare thiol-reactive surfaces by immobilizing the linker via its hydroxyl group, or to functionalize cysteine-containing molecules with a hydroxyl handle for further modification or enzymatic recognition (e.g., phosphorylation).
Molecular Weight
141.13
Purity
>98.0%
Formula
C₆H₇NO₃
Product Type
Heterobifunctional Crosslinkers
Group 1
Maleimide
Group 2
OH
Form (20 deg.C)
Solid
Storage Condition
-20°C
Molecular Structure
For Research Use Only | Not For Clinical Use
Related products
- N-(2-Aminoethyl)maleimide Hydrochloride Heterobifunctional Crosslinker (CAT#: OLY-1023-YS90)
- Propargyl Ether Homobifunctional Crosslinker (CAT#: OLY-1023-YS139)
- 3-Maleimidopropionic Acid (CAT#: OLY-1023-YS48)
- 4-Maleimidobutyric Acid NHS (GMBS) Heterobifunctional Crosslinker (CAT#: OLY-1023-YS107)
- t-Boc-N-amido-PEG4-acid PEGylation Crosslinker (CAT#: OLY-1023-YS116)
- 4-Maleimidobutyric Acid Heterobifunctional Crosslinker (CAT#: OLY-1023-YS10)
- 4-[3-(Trifluoromethyl)-3H-diazirin-3-yl]benzoic Acid (TDBA) Photo-reactive Crosslinker (CAT#: OLY-1023-YS33)
- t-Boc-N-amido-PEG6-acid PEGylation Crosslinker (CAT#: OLY-1023-YS115)
Online Inquiry
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
