O-(2-Aminoethyl)-O′-[2-(biotinylamino)ethyl]octaethylene glycol

≥95%

Reagent Code: #222388
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CAS Number 960132-48-3

science Other reagents with same CAS 960132-48-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 682.87 g/mol
Formula C₃₀H₅₈N₄O₁₁S
badge Registry Numbers
MDL Number MFCD08274600
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

Used in bioconjugation and molecular labeling due to its ability to link biomolecules with high specificity. The biotin group enables strong binding to streptavidin or avidin, making it ideal for detection and purification in immunoassays, ELISA, and flow cytometry. The octaethylene glycol spacer enhances solubility and reduces non-specific binding, while the amino groups allow covalent attachment to proteins, nucleic acids, or surfaces. Commonly applied in probe development, diagnostic kits, and targeted drug delivery systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿14,150.00
inventory 100mg
10-20 days ฿37,220.00
O-(2-Aminoethyl)-O′-[2-(biotinylamino)ethyl]octaethylene glycol
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Used in bioconjugation and molecular labeling due to its ability to link biomolecules with high specificity. The biotin group enables strong binding to streptavidin or avidin, making it ideal for detection and purification in immunoassays, ELISA, and flow cytometry. The octaethylene glycol spacer enhances solubility and reduces non-specific binding, while the amino groups allow covalent attachment to proteins, nucleic acids, or surfaces. Commonly applied in probe development, diagnostic kits, and targete

Used in bioconjugation and molecular labeling due to its ability to link biomolecules with high specificity. The biotin group enables strong binding to streptavidin or avidin, making it ideal for detection and purification in immunoassays, ELISA, and flow cytometry. The octaethylene glycol spacer enhances solubility and reduces non-specific binding, while the amino groups allow covalent attachment to proteins, nucleic acids, or surfaces. Commonly applied in probe development, diagnostic kits, and targeted drug delivery systems.

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