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- BDP FL DBCO
BDP FL DBCO
| 货号 | 规格 | 价格 | 货期 |
|---|---|---|---|
| A14F0 | 1 mg | 110.00$ | in stock |
| B14F0 | 5 mg | 210.00$ | in stock |
| C14F0 | 10 mg | 310.00$ | in stock |
| D14F0 | 25 mg | 410.00$ | in stock |
| E14F0 | 50 mg | 695.00$ | in stock |
| F14F0 | 100 mg | 1190.00$ | in stock |
BDP FL is a photostable borondipyrromethene for FAM (fluorescein) channel. The dye is compatible with filter sets for fluorescein.
This is DBCO (azadibenzocyclooctyne) derivative for copper free Click chemistry reaction with azides.
BDP FL 是一种用于 FAM（荧光素）通道的光稳定硼二吡咯亚甲基。 该染料与荧光素滤光片组兼容。
这是用于与叠氮化物的无铜点击化学反应的 DBCO（氮杂二苯并环辛炔）衍生物。
Absorption and emission spectra of BDP FL
BDP FL DBCO相关产品
dsGreen Gel Staining Solution, 10000×
dsGreen for staining dsDNA in gels.
dsGreen 用于在凝胶中染色 dsDNA。
Sulfo-Cyanine5-PEG3-Biotin
Conjugate of biotin with sulfo-Cyanine5 emitting in the far-red region of the spectrum.
生物素与在光谱的远红色区域发射的 sulfo-Cyanine5 的结合物。
BDP 650/665 alkyne
BDP 650/665 alkyne is a red emitting BODIPY dye derivative carrying a terminal alkyne group for a copper catalyzed conjugation with azides. Absorption and emission spectra of BDP 650/665 are designed to fit Cy5 channel of various instruments.
BDP 650/665 炔烃是一种发红光的 BODIPY 染料衍生物，带有一个末端炔烃基团，用于铜催化与叠氮化物的共轭。 BDP 650/665 的吸收和发射光谱旨在适应各种仪器的 Cy5 通道。
General properties
| Appearance: | orange solid 橙色固体 |
| Mass spec M+ increment: | 592.3 |
| Molecular weight: | 592.49 |
| CAS number: | 2360493-46-3 |
| Molecular formula: | C35H35N4BF2O2 |
| Solubility: | good in DMF, DMSO, DCM |
| Quality control: | NMR 1H, HPLC-MS (95%) |
| MSDS: | Download |
| Product specifications |
Spectral properties
| Excitation/absorption maximum, nm: | 503 |
| ε, L⋅mol−1⋅cm−1: | 92000 |
| Emission maximum, nm: | 509 |
| Fluorescence quantum yield: | 0.97 |
| CF260: | 0.015 |
| CF280: | 0.027 |
相关文献：
- Merlo, R.; Caprioglio, D.; Cillo, M.; Valenti, A.; Mattossovich, R.; Morrone, C.; Massarotti, A.; Rossi, F.; Miggiano, R.; Leonardi, A.; Minassi, A.; Perugino, G. The SNAP-tag technology revised: an effective chemo-enzymatic approach by using a universal azide-based substrate. Journal of Enzyme Inhibition and Medicinal Chemistry, 2021, 36(1), 85–97. doi: 10.1080/14756366.2020.1841182
- Islam, M.R.; Nguy, C.; Pandit, S.; Lyon, L.A. Design and Synthesis of Core–Shell Microgels with One‐Step Clickable Crosslinked Cores and Ultralow Crosslinked Shells. Macromolecular Chemistry and Physics, 2020, 221(19), 2000156. doi: 10.1002/macp.202000156