4 Results for "

strained alkyne probe

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "strained alkyne probe" in MCE Product Catalog:

Cat. No.: HY-W800696
CAS No.: 2644752-86-1
BP Fluor 430 Azide is a water-soluble, green-fluorescent, azide-activated probe that reacts with terminal alkynes via a copper-catalyzed click reaction (CuAAC). It also reacts with strained cyclooctyne via a copper-free click chemistry reaction to form a stable triazole and does not require a Cu-catalyst or elevated temperatures. BP Fluor 430 is a bright, photostable, green-fluorescent probe with excitation near its absorption maximum at 432 nm and emission maximum at 539 nm. This probe is water soluble and pH-insensitive from pH 4 to pH 10. A next generation probe, BP Fluor 430 Picolyl Azide, is also available for detection of low abundance alkyne-tagged biomolecules.
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Cat. No.: HY-W800692
CAS No.: 2644752-84-9
BP Fluor 350 Azide is a blue-fluorescent, azide-activated probe that reacts with terminal alkynes via a copper-catalyzed click reaction (CuAAC). It also reacts with strained cyclooctyne via a copper-free click chemistry reaction to form a stable triazole and does not require Cu-catalyst or elevated temperatures. BP Fluor 350 is a water-soluble, moderately photostable, blue-fluorescent probe optimally excited by the 350 nm laser line. It is routinely used for generation of stable signal in imaging and flow cytometry. The brightness and photostability of blue dyes are best suited to direct imaging of high-abundance targets.
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Cat. No.: HY-D3501
Research Areas:  

Others

5-FAM BCN is a reactive fluorophore-labeled strained alkyne probe and bicyclononyne. 5-FAM BCN undergoes inverse-electron-demand Diels-Alder cycloaddition with five-membered cyclic dienes. 5-FAM BCN facilitates bioorthogonal bioconjugation reactions .
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Cat. No.: HY-W800691
CAS No.: 2644752-83-8
Target:  

Fluorescent Dye

Research Areas:  

Others

BP Fluor 350 Picolyl Azide is a blue-fluorescent azide-activated probe that reacts with terminal alkynes via a copper-catalyzed click reaction (CuAAC). It also reacts with strained cyclooctyne via a copper-free click chemistry reaction to form a stable triazole and does not require Cu-catalyst or elevated temperatures.
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