Produkte
Reagenzien für die Oligonukleotidsynthese
Click-Chemie-Phosphoramidite und -Trägermaterialien
DBCO-Serinol phosphoramidite

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DBCO-Serinol phosphoramidite

Oligonukleotidsynthese Kupferfreie Click-Chemie

Artikel-Nr.	Packungseinheit	Preis	Vorlaufzeit	Jetzt kaufen
6022-50umol	50 umol	$189.00	Auf Lager
6022-250mg	250 mg	$989.00	Auf Lager

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Incorporation of DBCO‑Serinol at a defined position within the oligonucleotide chain yields a reactive alkyne group ready for highly selective, bioorthogonal conjugation with azide‑bearing molecules via strain‑promoted azide–alkyne cycloaddition (SPAAC). Because this reaction does not require copper catalysts, it can be performed under mild conditions, including in the presence of living cells or sensitive biomacromolecules.

The modified oligonucleotides can be conjugated with fluorophores, biotin, peptides, polymers, nanoparticles, and other partners. This enables the preparation of probes for hybridization‑based assays (FISH, microarrays), aptamers, delivery conjugates, and DNA nanostructures.

Recommendations for using the reagent:

During synthesis, it is important to replace the standard iodine oxidation with an alternative oxidizer (CSO), as the DBCO group is sensitive to iodine; otherwise, the reagent is compatible with standard solid‑phase synthesis protocols and subsequent purification by HPLC or PAGE.

Struktur von DBCO-Serinol-Phosphoramidit

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General properties

Appearance:	beige powder
Molecular weight:	909.08
Molecular formula:	C₅₄H₆₁N₄O₇P
Solubility:	acetonitrile, dichloromethane, DMSO, DMF
Quality control:	NMR ¹H and ³¹P, (95 %+), HPLC-MS (90 %)
Storage conditions:	12 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate.
Sicherheitsdatenblatt:	herunterladen
	Product specifications

Oligo synthesis details

Diluent:	Anhydrous acetonitrile
Coupling conditions:	10-12 minutes at room temperature
Deprotection conditions:	stable to deprotection with ammonium hydroxide for 2 hours at 65 °C or overnight at room temperature. Compatible with AMA for deprotection, showing only slight degradation of the cyclooctyne after 2 hours. Oxidation: for oxidation step recommended to use 0.5 M CSO in anhydrous acetonitrile, Iodine oxidation is suitable to no more than 8-10 cycles.

This Product is offered and sold for research purposes only. It has not been tested for safety and efficacy in food, drug, medical device, cosmetic, commercial or any other use. Supply does not express or imply authorization to use for any other purpose, including, without limitation, in vitro diagnostic purposes, in the manufacture of food or pharmaceutical products, in medical devices or in cosmetic products.