N-(5-AMinopentyl)biotinamide trifluoroacetate salt

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Reagent Code: #218392
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CAS Number 288259-39-2

science Other reagents with same CAS 288259-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 442.50 g/mol
Formula C₁₇H₂₉F₃N₄O₄S
badge Registry Numbers
MDL Number MFCD03452814
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in bioconjugation and affinity labeling applications, this compound serves as a key reagent for attaching biotin to biomolecules such as proteins, peptides, or antibodies. Its primary function is to enable detection, purification, or immobilization of target molecules through strong streptavidin-biotin interactions. The amine-reactive nature allows it to form stable amide bonds with carboxyl groups when activated, making it suitable for labeling strategies in immunoassays, flow cytometry, and pull-down assays. The trifluoroacetate salt form enhances solubility and stability in common organic and aqueous-organic solvents, facilitating use in diverse biochemical workflows. Commonly employed in proteomics and molecular biology research for tagging and isolation of biomolecular complexes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,400.00
inventory 250mg
10-20 days ฿19,000.00

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N-(5-AMinopentyl)biotinamide trifluoroacetate salt
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Used in bioconjugation and affinity labeling applications, this compound serves as a key reagent for attaching biotin to biomolecules such as proteins, peptides, or antibodies. Its primary function is to enable detection, purification, or immobilization of target molecules through strong streptavidin-biotin interactions. The amine-reactive nature allows it to form stable amide bonds with carboxyl groups when activated, making it suitable for labeling strategies in immunoassays, flow cytometry, and pull-d

Used in bioconjugation and affinity labeling applications, this compound serves as a key reagent for attaching biotin to biomolecules such as proteins, peptides, or antibodies. Its primary function is to enable detection, purification, or immobilization of target molecules through strong streptavidin-biotin interactions. The amine-reactive nature allows it to form stable amide bonds with carboxyl groups when activated, making it suitable for labeling strategies in immunoassays, flow cytometry, and pull-down assays. The trifluoroacetate salt form enhances solubility and stability in common organic and aqueous-organic solvents, facilitating use in diverse biochemical workflows. Commonly employed in proteomics and molecular biology research for tagging and isolation of biomolecular complexes.

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