Product synthetic-chemistry-click-chemistry-dbco

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Catalog	name	Description	price
R-M1-8833	alpha-Man-N3	Alpha-Man-N3 combines the enzymatic activity of alpha-mannosidase with the reactivity of the azide group for selective bioconjugation through click chemistry. It is commonly used in applications such as glycosylation studies, protein modification, labeling, and detection in glycobiology and biotechnology research.	price>
R-M1-8834	alpha-Man-TEG-N3	alpha-Man-TEG-N3 combines the enzymatic activity of alpha-mannosidase, the hydrophilic properties of the TEG linker, and the reactivity of the azide group for selective bioconjugation through click chemistry. It is commonly employed in glycosylation studies, protein modification, labeling, and detection in glycobiology and biotechnology research.	price>
R-M1-8835	alpha-Man-TEG-Alkyne	alpha-Man-TEG-Alkyne combines the enzymatic activity of alpha-mannosidase, the hydrophilic properties of the TEG linker, and the reactivity of the alkyne group for selective bioconjugation through click chemistry. It finds applications in glycosylation studies, protein modification, labeling, and detection in the fields of glycobiology and biotechnology.	price>
R-M1-8836	Biotin-PEG(4)-Dde-N3	Biotin-PEG(4)-Dde-N3 combines the high affinity of biotin for avidin or streptavidin, the flexibility and steric distance of the PEG linker, the selective protection of the amine group with the Dde protecting group, and the reactivity of the azide group for selective bioconjugation through click chemistry. It is commonly used for biotinylation of biomolecules, protein purification, and for generating biotinylated probes for various detection and labeling applications in biological and biomedical research.	price>
R-M1-8844	N3-TFBA-O2Oc,cas1993119-45-1	N3-TFBA-O2Oc represents a molecule that combines an azide group (N3), a trifluoroborane anion (TFBA), and an organic moiety containing two oxygen atoms bonded to a carbon atom (O2Oc). The function and potential applications of this molecule would depend on the specific nature and reactivity of the O2Oc moiety.	price>
R-M1-8846	TCO-triethoxysilane,cas2714298-10-7	TCO-triethoxysilane combines the TCO group with a triethoxysilane moiety, potentially enabling the covalent coupling of TCO to materials or molecules containing reactive groups like tetrazines. This molecule can be used in various applications, such as the functionalization of surfaces or the synthesis of TCO-modified polymers or materials.	price>
R-M1-8899	DBCO-NH-PEG1-CH2CH2COONHS ester	DBCO-NH-PEG1-CH2CH2COONHS ester represents a versatile compound for bioconjugation and biochemistry, offering a platform for the functionalization and modification of various biomaterials, surfaces, or nanoparticles. It allows for the selective and controlled conjugation of molecules, contributing to the development of tailored bioconjugates with specific properties and functionalities for various biomedical and biotechnological applications.	price>
R-M-5448	TAMRA DBCO	TAMRA DBCO reacts with azides via a copper-free “click chemistry” reaction to form a stable triazole and does not require Cu-catalyst or elevated temperatures. This copper-free variation of click reaction overcomes a major shortcoming of copper-catalyzed click reaction – the need for copper catalyst. Copper can damage fluorescent proteins, Quantum Dot nanocyrstals, certain enzymes, and photoproteins like RPE. The presence of copper is also problematic in staining the surface of live cells.In application where the presence of copper is a concern TAMRA DBCO is an ideal alternative to copper requiring fluorescent alkynes.	price>
R-M1-8983	6-Azide-Trehalose (6-TreAz)	6-Azide-Trehalose is a compound that is often used in chemical biology, bioconjugation, and glycobiology research.The azide group can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAC) or "click chemistry" with alkynes or other compounds containing terminal alkynes. This property makes 6-Azide-Trehalose valuable in bioorthogonal labeling and functionalization of biomolecules, as well as in metabolic labeling and imaging studies. The trehalose backbone also provides stability and protection to the azide group, allowing for specific targeting and conjugation without compromising the functional group.	price>
R-M1-9043	endo-BCN-NHS carbonate,cas1426827-79-3	endo-BCN-NHS carbonate is a chemical compound used in bioconjugation and bioorthogonal chemistry. The compound contains an endo-BCN (bicyclo[6.1.0]non-4-ene) group, an NHS (N-hydroxysuccinimide) ester, and a carbonate functional group. The endo-BCN group can participate in copper-free click chemistry reactions with tetrazine-functionalized molecules, allowing for specific and selective labeling or modification of biomolecules. The NHS ester provides a means for coupling the compound to primary amines, such as those present in proteins or nucleic acids, and the carbonate functional group may contribute to the stability and reactivity of the compound.	price>

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