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6-OG488 Azide
6-OG488 azide has the same chemical structure to that of Oregon Green™ 488 azide. It is a convenient tool to introduce the fluorophore of Oregon Green to a biological molecule that contains an alkyne group. It is reactive with terminal alkynes via a copper-catalyzed click reaction. In particular, 6-OG488 azide can be used as a bio-orthogonal or biologically unique hapten for the biological applications requiring signal amplification. Oregon Green is a bright and photostable alternative to fluorescein for use in flow cytometry, fluorescence microscopy and high content analysis of cells. Oregon Green™ is the trademark of ThermoFisher.
Spectrum
Product family
| Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) | Correction Factor (280 nm) |
| 6-FAM Azide | 493 | 517 | 83000 | 0.178 |
| 6-HEX azide | 533 | 559 | 73000 | 0.15 |
| 6-TET azide | 521 | 542 | 73000 | 0.13 |
| 6-JOE azide | 520 | 545 | 750001 | - |
| 6-TAMRA azide | 552 | 578 | 90000 | 0.178 |
| 6-ROX azide | 578 | 604 | 82000 | 0.168 |
| 6-OG488 acid [equivalent to Oregon Green® 488 carboxylic acid, 6-isomer] | 498 | 526 | 76000 | 0.12 |
| 6-NED azide | 545 | 567 | 740001 | - |
| 6-VIC Azide | 526 | 543 | - | - |
References
View all 50 references: Citation Explorer
Photoactivatable Fluorescent Tags for Dual-Modality Positron Emission Tomography Optical Imaging.
Authors: Guillou, Amaury and Nisli, Eda and Klingler, Simon and Linden, Anthony and Holland, Jason P
Journal: Journal of medicinal chemistry (2022): 811-823
Authors: Guillou, Amaury and Nisli, Eda and Klingler, Simon and Linden, Anthony and Holland, Jason P
Journal: Journal of medicinal chemistry (2022): 811-823
Selective Mitochondrial Protein Labeling Enabled by Biocompatible Photocatalytic Reactions inside Live Cells.
Authors: Wang, Haoyan and Zhang, Yixin and Zeng, Kaixing and Qiang, Jiali and Cao, Ye and Li, Yunxia and Fang, Yanshan and Zhang, Yaoyang and Chen, Yiyun
Journal: JACS Au (2021): 1066-1075
Authors: Wang, Haoyan and Zhang, Yixin and Zeng, Kaixing and Qiang, Jiali and Cao, Ye and Li, Yunxia and Fang, Yanshan and Zhang, Yaoyang and Chen, Yiyun
Journal: JACS Au (2021): 1066-1075
Cell-surface Labeling via Bioorthogonal Host-Guest Chemistry.
Authors: Kataki-Anastasakou, Anna and Hernandez, Selena and Sletten, Ellen M
Journal: ACS chemical biology (2021): 2124-2129
Authors: Kataki-Anastasakou, Anna and Hernandez, Selena and Sletten, Ellen M
Journal: ACS chemical biology (2021): 2124-2129
Interfacial dilatational and emulsifying properties of ultrasound-treated pea protein.
Authors: Sha, Lei and Koosis, Aeneas O and Wang, Qingling and True, Alma D and Xiong, Youling L
Journal: Food chemistry (2021): 129271
Authors: Sha, Lei and Koosis, Aeneas O and Wang, Qingling and True, Alma D and Xiong, Youling L
Journal: Food chemistry (2021): 129271
Design and Synthesis of Fluorophore-Tagged Disparlure Enantiomers to Study Pheromone Enantiomer Discrimination in the Pheromone-Binding Proteins from the Gypsy Moth, Lymantria dispar.
Authors: Pinnelli, Govardhana R and Plettner, Erika
Journal: Journal of chemical ecology (2021)
Authors: Pinnelli, Govardhana R and Plettner, Erika
Journal: Journal of chemical ecology (2021)
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