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BD Horizon RealBlue™ 744 Reagents

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A Bright Option for High Parameter and Spectral Flow Cytometry Panels

BD Horizon RealBlue™ 744 (RB744) Reagents leverage an innovative laser-specific fluorochrome, excited primarily by the 488-nm blue laser to offer:
 

  • Minimal cross-laser excitation off the 561-nm yellow-green laser
  • A bright fluorochrome to support the detection of low-expression surface and intracellular markers
  • Compatibility with appropriately configured* conventional and spectral flow cytometers

*Filter centered near 750 nm, e.g., 750/30
 
RB744 vials
performance1

RB744 Reagents Can Be Used in High Parameter Flow Cytometry Panels to Increase Biological Resolution

RB744 specifications

 

FormatEx MaxEm MaxSpectralConventionalRelative BrightnessSpillover* (1 = low, 4 = high)Alternative To
RB744498 nm746 nm✓✓ 1BB755-P
 
*Value may vary based on instrument configuration and settings. Spillover ranking is based on cross-laser excitation on five-laser spectral instruments and does not take into account spillover into adjacent detectors.
 

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Performance

BD Horizon RealBlue™ 744 Reagents Provide Minimal Cross-laser Excitation Off the 561-nm Yellow-green Laser

 

RB744 has minimal cross-laser excitation

RB744 Minimum Cross Laser Excitation

Normalized emission profile of RB744. Human CD4 SK3 antibody acquired on a BD FACSDiscover™ S8 Cell Sorter.

RB744 is a very bright fluorochrome with minimal spillover spread into RY743
RB744 Brightness and minimal Spillover

Human whole blood was stained with BD Horizon™ RB744 Human CD4 Reagent (clone SK3), acquired on a BD FACDiscover™ S8, and unmixed with BUV737, BV750, RY743 or R718 (clone SK3) using FlowJo™ Software. Single-color overlays are shown.


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Applications

Multicolor Flow Cytometry

BD Horizon™ RB744 Reagents Have Excellent Resolution as Demonstrated in a 17-color Spectral Flow Cytometry Panel Acquired on the BD FACSymphony™ A5 SE Cell Analyzer

 

Gating strategy for detection of T cell subsets in activated T cells
RB744 T cell subset gating strategy

Peripheral blood mononuclear cells were isolated and loaded with BD Horizon™ Violet Proliferation Dye 450 before stimulation with or without staphylococcal enterotoxin B (SEB, 1 µg/mL) and CD28 (1 µg/mL) for 3 days. PMA (10 ng/mL) and ionomycin (1 µg/mL) were added to the Stimulated + Boost group 4 hours before collecting cells for staining. Cells were then stained with BD Horizon™ Fixable Viability Stain 620 and antibodies against cell surface markers prior to fixing and permeabilizing with BD Cytofix/Cytoperm™ Fixation/Permeabilization Buffer. Fixed and permeabilized cells were then stained with intracellular antibodies. Stained cells were analyzed on a BD FACSymphony™ A5 SE Cell Analyzer. Gating strategy for detection of T cell subsets after exclusion of doublets, dead cells and lineage-positive cells: CD3+ T cells were selected and divided into CD4+ or CD8+ cells. CD8+ T cells were further evaluated for activation stage based on their expression of CD25 and CD69. Samples were acquired on a BD FACSymphony™ A5 SE Cell Analyzer and analyzed with FlowJo™ Software.

Expression of inhibitory receptors at different activation levels of CD8+ T cells
RB744 CD8+Tcell Activation Inhibitory Receptor Expresseion

Histogram overlays showing expression of inhibitory receptors on CD8+ T cell subsets from the Stimulated group. Total CD8+ T cells from the Unstimulated group (top, dark green).

Cytokines expression at different activation stages of CD8+ T cells
CD8+ T cell Activation Inracellular Cytokine Expression

Histogram overlays showing expression of cytokines on CD8+ T cell subsets from the Stimulated + Boost group. Total CD8+ T cells from the Unstimulated group (top, dark green).

Fluorochrome marker assignment for a 17-color spectral flow cytometry panel

 

 SpecificityCloneFluorochrome
UV
355 nm

CD25

M-A251

BUV395

CD56

NCAM16.2

BUV496

CD20

L27

BUV496

CD19

SJ25C1

BUV496

CD16

3G8

BUV496

CD14

M5E2

BUV496

AutoF

N/A

N/A

TIM-3

7D3

BUV615

CD4

SK3

BUV805

Violet
405 nm

TNF

MAb11

BV421

VPD450

N/A

N/A

CD3

UCHT1

BV510

CD134

ACT35

BV786

Blue
488 nm

IFNγ

B27

FITC

CD69

FN50

RB545

FVS620

N/A

N/A

LAG-3

T47-530

RB705

PD-1

EH12.1

RB744

II-2

MQ1-17H12

RB780

Yellow-Green
561 nm

CTLA-4

BNI3

RY586

Red
640 nm

GranzB

GB11

AF647

CD8

SK1

APC-H7


Fluorochrome marker assignment for a 17-color spectral flow cytometry panel acquired on the BD FACSymphony™ A5 SE Cell Analyzer.


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Buffer Compatibility

BD Horizon RealBlue™ 744 Reagents Are Compatible with a Broad Range of Fixation and Permeabilization Systems

 

BuffersResults
BD FACS™ Lysing Solution and BD Pharm Lyse™ Lysing BufferCompatible
CellBlox™ Blocking BufferCompatible
BD Cytofix™ Fixation BufferStable at least 24 hours
1% PFAStable at least 24 hours
BD Cytofix/Cytoperm™ Fixation and Permeabilization SolutionCompatible with antibody staining before and after fixation
BD FACS™ Permeabilizing Solution 2Compatible with antibody staining before and after fixation
BD Phosflow™ Perm Buffer IIICompatible with antibody staining before and after fixation
EDTA and HeparinCompatible
BD Horizon™ Brilliant Stain Buffer (BSB)Compatible
 

   

   

BD flow cytometers are Class 1 Laser Products. For Research Use Only. Not for use in diagnostic or therapeutic procedures.

CF is a trademark of Biotium, Inc. Cy is a trademark of Global Life Sciences Solutions Germany GmbH or an affiliate doing business as Cytiva. CellBlox is a trademark of Thermo Fisher Scientific.