Spectraviewer image of Brilliant Ultra Violet 563 dye

Brilliant Ultra Violet™ dyes, including Brilliant Ultra Violet™ 563 (BUV563), are a polymer dye-based technology and compatible with both spectral flow cytometry, as well as traditional flow cytometry. The UV laser has unique channels far from heavily occupied detectors allowing for larger panels.

BUV563 is a tandem dye excited by the 355 nm UV laser and emits at 563 nm. This dye has a medium-to-high relative brightness and can be used for cell surface, intracellular, and nuclear staining.

When using two or more Super Bright, Brilliant Violet, Brilliant Ultra Violet™, or other polymer dye- conjugated antibodies in a staining panel, we recommend that you use Super Bright Complete Staining Buffer (Cat. No. SB-4401-42) or Brilliant Stain Buffer (Cat. No. 00-4409-42) to minimize any non- specific polymer interactions.

BUV563 dye dashboard


Initial brightness
 
 
 
 
 
The UV laser-excitable BUV563 dye is optimized for use both cell surface and intracellular flow applications. Can be used for spectral flow cytometry applications. 

Photostability in buffer
 
 
 
 
 
 355585/15*,
535 LP		350564 
 
Laser line
Filter
Excitation max


Emission max

 

*Instruments with yellow-green (561 nm) laser. Without yellow-green laser: 560/40, 535 LP.

BUV563 dye products

We offer BUV563 dye conjugated to primary antibodies for use in flow cytometry.

Antibody conjugates

Brilliant Stain Buffer
Super Bright Staining Buffer

Experimental data using BUV563 dye products

Figure 1. Excitation and emission of Brilliant Ultra Violet™ 563 dye (BUV563).

Figure 2. Spectral signature of BUV563 dye. Data acquired on a 5-laser Cytek Aurora and normal human peripheral blood cells stained with clone SK7 (hCD3) conjugated to BUV563 (Cat. No. 365-0036-42) were used for analysis.

Dot plot of Ki-67 BUV563 vs CD45R (B220) FITC in unstimulated and stimulated cells

Figure 3. C57BL/6 mouse splenocytes were unstimulated (left) or stimulated for 48 hours with CD3e Monoclonal Antibody, Functional Grade (Cat. No. 16-0031-85) (right). Cells were then stained intracellularly, using the Foxp3/Transcription Factor Staining Buffer Set (Cat. No. 00-5523-00) and protocol, with CD45R (B220) Monoclonal Antibody, FITC (Cat. No. 11-0452-82) and 1.0 µg of Ki-67 Monoclonal Antibody, Brilliant Ultra Violet™ 563 dye (Cat. No. 365-5698-82). Viable cells in the lymphocyte gate were used for analysis, as determined by LIVE/DEAD™ Fixable Blue Dead Cell Stain Kit (Cat. No. L34962).

Dot plot of samples stained with IgG1 control vs CD3-FITC and CD19-BUV563 vs CD3-FITC

Figure 4. Normal human peripheral blood cells were stained with CD3 Monoclonal Antibody, FITC (Cat. No. 11-0038-42) and Mouse IgG1 kappa Isotype Control, Brilliant Ultra Violet™ 563 dye (Cat. No. 365-4714-81) (left) or CD19 Monoclonal Antibody, Brilliant Ultra Violet™ 563 dye (Cat. No. 365-0199-42) (right). Viable cells in the lymphocyte gate were used for analysis, as determined by 7-AAD (Cat. No. 00-6993-50).

BRILLIANT ULTRA VIOLET™ is a trademark or registered trademark of Becton, Dickinson and Company or its affiliates, and is used under license. Powered by Sirigen™.

Brilliant Ultra Violet™ and Brilliant Violet™ are trademarks or registered trademarks of Becton, Dickinson and Company or its affiliates, and is used under license.

仅供科研使用，不可用于诊断目的。