Mal-PEG2-NH2 (TFA)

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Reagent Code: #82182
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CAS Number 660843-23-2

science Other reagents with same CAS 660843-23-2

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Weight 342.27 g/mol
Formula C₁₂H₁₇F₃N₂O₆
inventory_2 Storage & Handling
Storage Room temperature, dark, dry, inert gas

description Product Description

Mal-PEG2-NH2 (TFA) is widely used in bioconjugation and drug delivery applications. It serves as a linker molecule, enabling the attachment of therapeutic agents, proteins, or peptides to other biomolecules or nanoparticles. The maleimide group reacts selectively with thiol groups, facilitating stable covalent bonds, while the amine group allows for further functionalization or coupling with carboxyl groups. This compound is particularly valuable in antibody-drug conjugates (ADCs), where it helps in creating targeted cancer therapies by linking cytotoxic drugs to antibodies. Additionally, it is employed in surface modification of nanoparticles to enhance their biocompatibility and targeting efficiency. Its water solubility and stability make it a preferred choice in various biomedical and pharmaceutical research applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿24,255.00

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Mal-PEG2-NH2 (TFA)
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Mal-PEG2-NH2 (TFA) is widely used in bioconjugation and drug delivery applications. It serves as a linker molecule, enabling the attachment of therapeutic agents, proteins, or peptides to other biomolecules or nanoparticles. The maleimide group reacts selectively with thiol groups, facilitating stable covalent bonds, while the amine group allows for further functionalization or coupling with carboxyl groups. This compound is particularly valuable in antibody-drug conjugates (ADCs), where it helps in crea

Mal-PEG2-NH2 (TFA) is widely used in bioconjugation and drug delivery applications. It serves as a linker molecule, enabling the attachment of therapeutic agents, proteins, or peptides to other biomolecules or nanoparticles. The maleimide group reacts selectively with thiol groups, facilitating stable covalent bonds, while the amine group allows for further functionalization or coupling with carboxyl groups. This compound is particularly valuable in antibody-drug conjugates (ADCs), where it helps in creating targeted cancer therapies by linking cytotoxic drugs to antibodies. Additionally, it is employed in surface modification of nanoparticles to enhance their biocompatibility and targeting efficiency. Its water solubility and stability make it a preferred choice in various biomedical and pharmaceutical research applications.

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