- 215312-86-0
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- $1.00 / 1KG
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2019-09-02
- CAS:215312-86-0
- Min. Order: 1KG
- Purity: ≥98%
- Supply Ability: 200KG
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| | 6-MALEIMIDOCAPROIC ACID SULFO-N-SUCCINIMIDYL ESTER Basic information |
| | 6-MALEIMIDOCAPROIC ACID SULFO-N-SUCCINIMIDYL ESTER Chemical Properties |
| Melting point | 158-165°C | | storage temp. | 2-8°C | | solubility | DMSO (Slightly, Sonicated) | | form | Solid | | color | White to Pale Yellow | | Stability: | Moisture Sensitive |
| | 6-MALEIMIDOCAPROIC ACID SULFO-N-SUCCINIMIDYL ESTER Usage And Synthesis |
| Chemical Properties | White Solid | | Uses | A water soluble sulfhydryl and amio reactive heterobifunctional crosslinking reagent.Spacer Arm: 9.4 Angstroms | | Uses | A water soluble sulfhydryl and amio reactive heterobifunctional crosslinking reagent.
Spacer Arm: 9.4 Angstroms | | General Description | EMCS and its water-soluble analog Sulfo-EMCS are heterobifunctional cross-linkers that contain N-hydroxysuccinimide (NHS) ester and maleimide groups that allow covalent conjugation of amine- and sulfhydryl-containing molecules. NHS esters react with primary amines at pH 7-9 to form amide bonds, while maleimides react with sulfhydryl groups at pH 6.5-7.5 to form stable thioether bonds. In aqueous solutions, hydrolytic degradation of the NHS ester is a competing reaction whose rate increases with pH. The maleimide group is more stable than the NHS-ester group but will slowly hydrolyze and also lose its reaction specificity for sulfhydryls at pH values > 7.5. For these reasons, conjugation experiments involving these cross-linkers are usually performed at pH 7.2-7.5, with the NHS-ester (amine-targeted) reaction being accomplished before or simultaneous with the maleimide (sulfhydryl-targeted) reaction. |
| | 6-MALEIMIDOCAPROIC ACID SULFO-N-SUCCINIMIDYL ESTER Preparation Products And Raw materials |
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