Mal-amido-PEG9-NHS ester

≥95%

Reagent Code: #108860
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CAS Number 2575631-92-2

science Other reagents with same CAS 2575631-92-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 733.76 g/mol
Formula C₃₂H₅₁N₃O₁₆
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Mal-amido-PEG9-NHS ester is a heterobifunctional crosslinker used in bioconjugation to link biomolecules such as proteins, peptides, and antibodies with other molecules or surfaces. The maleimide (Mal) group enables specific reaction with thiol (-SH) groups on cysteine residues, while the NHS ester group forms stable covalent bonds with primary amine-containing compounds. The PEG9 spacer enhances solubility, reduces steric hindrance, and minimizes non-specific interactions, thereby improving overall reaction efficiency. It is commonly applied in drug delivery systems to develop targeted therapies and in diagnostic assays for biomolecule labeling and detection purposes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,400.00

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Mal-amido-PEG9-NHS ester
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Mal-amido-PEG9-NHS ester is a heterobifunctional crosslinker used in bioconjugation to link biomolecules such as proteins, peptides, and antibodies with other molecules or surfaces. The maleimide (Mal) group enables specific reaction with thiol (-SH) groups on cysteine residues, while the NHS ester group forms stable covalent bonds with primary amine-containing compounds. The PEG9 spacer enhances solubility, reduces steric hindrance, and minimizes non-specific interactions, thereby improving overall reac

Mal-amido-PEG9-NHS ester is a heterobifunctional crosslinker used in bioconjugation to link biomolecules such as proteins, peptides, and antibodies with other molecules or surfaces. The maleimide (Mal) group enables specific reaction with thiol (-SH) groups on cysteine residues, while the NHS ester group forms stable covalent bonds with primary amine-containing compounds. The PEG9 spacer enhances solubility, reduces steric hindrance, and minimizes non-specific interactions, thereby improving overall reaction efficiency. It is commonly applied in drug delivery systems to develop targeted therapies and in diagnostic assays for biomolecule labeling and detection purposes.

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