PerCP-Cy5.5 Tandem
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Physical properties
Molecular weight | N/A |
Solvent | Water |
Spectral properties
Extinction coefficient (cm -1 M -1) | 350000 |
Excitation (nm) | 482 |
Emission (nm) | 695 |
Storage, safety and handling
Certificate of Origin | Download PDF |
H-phrase | H303, H313, H333 |
Hazard symbol | XN |
Intended use | Research Use Only (RUO) |
R-phrase | R20, R21, R22 |
Storage | Refrigerated (2-8 °C); Minimize light exposure |
UNSPSC | 12171501 |
Overview | SDSProtocol |
Molecular weight N/A | Extinction coefficient (cm -1 M -1) 350000 | Excitation (nm) 482 | Emission (nm) 695 |
PerCP (Peridinin-chlorophyll-protein complex) is isolated from Dinophyceae sp. It has an extremely high extinction coefficient, a high quantum efficiency and a large Stokes shift. It is well excited with the Argon laser at 488 nm with its maximum emission peak at 677 nm. PerCP protein is commonly used for fluorescent immunolabeling, particularly in applications involving fluorescent-activated cell sorting (FACS). Its tandem conjugates (such as PerCP-Cy5.5) can be excited with a standard 488 nm laser and emits in the far red at a longer wavelength for multicolor flow cytometric analysis of cells. These multiple emission wavelengths make PerCP- Cyanine conjugates potentially useful fluorochromes for multicolor analysis with FITC, PE and other fluorochromes. PerCP tandem structure may make it more photostable than PerCP alone, which generally photobleaches rapidly with more powerful water-cooled gas lasers.
Spectrum
Open in Advanced Spectrum Viewer
Spectral properties
Extinction coefficient (cm -1 M -1) | 350000 |
Excitation (nm) | 482 |
Emission (nm) | 695 |
Product Family
Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) |
PE-Cy5.5 Tandem | 565 | 671 | 1960000 |
APC-Cy5.5 Tandem | 651 | 700 | 700000 |
Images
References
View all 2 references: Citation Explorer
Four color compensation.
Authors: Stewart, C C and Stewart, S J
Journal: Cytometry (1999): 161-75
Authors: Stewart, C C and Stewart, S J
Journal: Cytometry (1999): 161-75
A strategy for multiple immunophenotyping by image cytometry: model studies using latex microbeads labeled with seven streptavidin-bound fluorochromes.
Authors: Gothot, A and Grosdent, J C and Paulus, J M
Journal: Cytometry (1996): 214-25
Authors: Gothot, A and Grosdent, J C and Paulus, J M
Journal: Cytometry (1996): 214-25
Application notes
A New Protein Crosslinking Method for Labeling and Modifying Antibodies
A Novel Fluorescent Probe for Imaging and Detecting Hydroxyl Radical in Living Cells
Buccutite™ Bioconjugation Technology
Monitoring of Mitochondrial Membrane Potential Changes in Live Cells Using JC-10
Multiplexing Cell Proliferation and Cytotoxicity Assays Using Calcein Red and CytoCalceins
A Novel Fluorescent Probe for Imaging and Detecting Hydroxyl Radical in Living Cells
Buccutite™ Bioconjugation Technology
Monitoring of Mitochondrial Membrane Potential Changes in Live Cells Using JC-10
Multiplexing Cell Proliferation and Cytotoxicity Assays Using Calcein Red and CytoCalceins
FAQ
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Can I intracellularly measure mitochondria calcium flux and changes in mitochondria membrane potential at the same time?