Sulfo-DBCO-NHS ester

95%

Reagent Code: #235823
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CAS Number 1379761-19-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 504.44 g/mol
Formula C₂₃H₁₇N₂NaO₈S
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in bioconjugation for labeling biomolecules such as proteins, peptides, and antibodies in aqueous solutions. The DBCO group reacts rapidly and selectively with azide-functionalized molecules via copper-free click chemistry, making it ideal for live-cell labeling and in vivo applications where copper toxicity is a concern. The sulfo-NHS ester group enables efficient coupling to primary amines (e.g., lysine residues) under mild conditions, forming stable amide bonds. Commonly applied in the development of antibody-drug conjugates, fluorescent probes, and functionalized nanoparticles. Water solubility from the sulfo group eliminates the need for organic solvents, improving biocompatibility and simplifying reaction setup.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿60,310.00
Sulfo-DBCO-NHS ester
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Used in bioconjugation for labeling biomolecules such as proteins, peptides, and antibodies in aqueous solutions. The DBCO group reacts rapidly and selectively with azide-functionalized molecules via copper-free click chemistry, making it ideal for live-cell labeling and in vivo applications where copper toxicity is a concern. The sulfo-NHS ester group enables efficient coupling to primary amines (e.g., lysine residues) under mild conditions, forming stable amide bonds. Commonly applied in the developmen

Used in bioconjugation for labeling biomolecules such as proteins, peptides, and antibodies in aqueous solutions. The DBCO group reacts rapidly and selectively with azide-functionalized molecules via copper-free click chemistry, making it ideal for live-cell labeling and in vivo applications where copper toxicity is a concern. The sulfo-NHS ester group enables efficient coupling to primary amines (e.g., lysine residues) under mild conditions, forming stable amide bonds. Commonly applied in the development of antibody-drug conjugates, fluorescent probes, and functionalized nanoparticles. Water solubility from the sulfo group eliminates the need for organic solvents, improving biocompatibility and simplifying reaction setup.

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