BD Accuri™ C6 Cytometer
Flow cytometry within reach™
3
The BD Accuri™ C6 is a personal flow cytometer that brings cell analysis within reach by being easy to use, simple to maintain, and affordable.
Flow cytometry within reach
The analytical power and versatility of today’s laser-based flow cytometry systems have unlocked the mysteries of cell biology and empowered entirely new fields of research. As a result, flow cytometry has become a staple of modern laboratories around the world. Innovations in ease of use reflected in the BD Accuri C6 cytometer make these powerful capabilities more accessible to a new generation of flow cytometry users.
The compact footprint and transportable weight of the BD Accuri C6 also make it a valuable personal use tool for experienced researchers who want a cytometer to be easily available when and where they need it.
Many BD Accuri C6 cytometer users can begin collecting and analyzing data with the help of a quick start guide. The intuitive interface of the software guides the user through workflows. A wide dynamic range of over 7 full decades ensures that all data is available all of the time. Information obtained from the BD Accuri C6 can be re-analyzed at any time if gating or compensation changes are required, or to accommodate new research.
The BD Accuri C6 is small enough to easily fit on a benchtop and can be placed in a laminar flow hood if biohazard containment is required. It measures 11 x 14.75 x 16.5 inches (H x W x D) (27.9 x 37.5 x 41.9 cm) and weighs just 30 pounds (13.6 kg).
4
102 106103 104 105
010
050
Co
un
t
FITC CD45RA-A
A07 CD45_CD4_CD8_CD3Gate: (CD3+ CD8+ in (P1 in all))
V1-L15.5%
V1-R84.5%
V1-L15.5%
V1-R84.5%
101.7 106103 104 105101.
710
610
310
410
5PE
-Cy7
CD
8-A
APC CD3-A
A06 CD4_CD8_CD3Gate: (P1 in all)
CD3+ CD8+7.1%CD3+ CD8+7.1%
101.7 106103 104 105
101
106
102
103
104
105
PE C
D4-
A
APC CD3-A
A06 CD4_CD8_CD3Gate: (P1 in all)
CD3+ CD4+33.6%CD3+ CD4+33.6%
102 106103 104 105
030
010
020
0C
ou
nt
FITC CD45RA-A
A07 CD45_CD4_CD8_CD3Gate: (CD3+ CD4+ in (P1 in all))
V2-L V2-RV2-L V2-R
The system is equipped with a blue and red laser, two light scatter detectors, and four fluorescence detectors with optical filters optimized for the detection of FITC, PE, PerCP, and APC. A compact optical design, fixed alignment, and pre-optimized detector settings make the system easier to use.
Optional filters and the Selectable Laser Module expand the available fluorochrome combinations. During manufacture, laser and optical alignments are set and locked down. The result is that each BD Accuri C6 cytometer is manufactured with standardized fluorescence performance so that users do not need to adjust detector voltages.
Data is digitally collected over a wide dynamic range of 7.2 decades (16 million channels of digital data), making all data available to users as needed. Gating strategies and fluorescence compensation values can be set before, during, or after data collection. After data is collected, the BD Accuri™ C6 software Zoom function allows visualization of data at any scale, so that users can precisely set gates and regions.
Should updates in the values be required later, or if optimi-zation is needed, simply change the settings and re-analyze the data. This flexibility also allows data to be re-examined to accommodate new research findings.
The system has been put through intense testing to ensure that the design can withstand rugged conditions. Provided the system is anchored, it can run samples even if the benchtop is in motion, for example, onboard a ship.
Pre-optimized detectors,minimized setup time
T-cell phenotyping, 4-color analysisThawed human peripheral blood mononuclear cells (PBMCs) were stained with directly labeled anti-CD45RA FITC, CD4 PE, CD8 PE-Cy™7, and CD3 APC in PBS + 1 mg/mL of BSA, covered, on ice, for 30 minutes. Cells were acquired and gated on lymphocytes to identify CD3+CD8+ cytotoxic (blue) and CD3+CD4+ helper (red) T-cell populations.
After FITC staining, subpopulations of CD45RA+ and CD45RA– cytotoxic and helper T cells were identified.
O P T I C S
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Apoptosis detectionThe BD Accuri C6 can perform most flow cytometric apoptosis assays, including Annexin V, caspase activation, PARP cleavage, mitochondrial membrane potential (ΔΨm), and DNA fragmentation. (A) K562 cells (human chronic myelogenous leukemia) were treated with CCCP to induce apoptosis, then stained with JC-1 according to the BD™ MitoScreen (JC-1) protocol (Cat. No. 551302). The cells were washed and collected on the BD Accuri C6. CCCP treatment (C) resulted in a shift in ΔΨm (red to green) vs untreated cells (B), indicating apoptosis.
0 14,540,9695,000,000 10,000,000
05,
093,
085
2,00
0,00
0SS
C-A
FSC-A
A02 K562 untreated JC-1Gate: [No Gating]
P190.0%P190.0%
104.6 106.8105 106105.
110
710
6JC
-1 F
L-2-
A
JC-1 FL-1-A
A02 K562 untreated JC-1Gate: (P1 in all)
P987.6%
P1010.6%
P987.6%
P1010.6%
104.6 106.8105 106105.
110
710
6JC
-1 F
L-2-
A
JC-1 FL-1-A
A03 K562 CCCP JC-1 Gate: (P1 in all)
P912.9%
P1084.0%
P912.9%
P1084.0%
0 14,540,9695,000,000 10,000,000
05,
093,
085
2,00
0,00
0SS
C-A
FSC-A
A02 K562 untreated JC-1Gate: [No Gating]
P190.0%P190.0%
104.6 106.8105 106105.
110
710
6JC
-1 F
L-2-
A
JC-1 FL-1-A
A02 K562 untreated JC-1Gate: (P1 in all)
P987.6%
P1010.6%
P987.6%
P1010.6%
104.6 106.8105 106105.
110
710
6JC
-1 F
L-2-
A
JC-1 FL-1-A
A03 K562 CCCP JC-1 Gate: (P1 in all)
P912.9%
P1084.0%
P912.9%
P1084.0%
0 14,540,9695,000,000 10,000,000
05,
093,
085
2,00
0,00
0SS
C-A
FSC-A
A02 K562 untreated JC-1Gate: [No Gating]
P190.0%P190.0%
104.6 106.8105 106105.
110
710
6JC
-1 F
L-2-
A
JC-1 FL-1-A
A02 K562 untreated JC-1Gate: (P1 in all)
P987.6%
P1010.6%
P987.6%
P1010.6%
104.6 106.8105 106105.
110
710
6JC
-1 F
L-2-
A
JC-1 FL-1-A
A03 K562 CCCP JC-1 Gate: (P1 in all)
P912.9%
P1084.0%
P912.9%
P1084.0%
A B C
6
A unique low-pressure pumping system drives the fluidics. A sheath-focused core enables event rates of up to 10,000 events per second and a sample concentration of over 5 x 106 cells per mL. In addition, the system derives sample volume and can calculate absolute counts or sample concentration per microliter.
The non-pressurized system supports any brand of 12 x 75-mm (or smaller) sample tubes, including microcentrifuge tubes and tubes made of polypropylene or polystyrene. The BD Accuri C6 cytometer simplifies system maintenance with automatic cleaning cycles on instrument shutdown. The system can employ laboratory-grade water for sheath fluid, reducing operating costs.
For walkaway convenience, the optional BD CSampler™ accessory offers reliable and easy-to-use automation. The system supports 48- and 96-well plates and deep- well plates, and is also supplied with a 24-tube rack for standard 12 x 75-mm tubes. They are processed directly in the BD Accuri C6 cytometer, saving time. The BD CSampler adds minimal footprint to the BD Accuri C6, about three feet square for the pair, keeping the benchtop free for other uses.
To streamline sample processing, the BD CSampler allows multiple collection settings to be applied to plate or tube runs. To process a sample immediately, a run can be paused using the Interrupt function. When the priority operation is complete, the original plate can be returned to the BD CSampler to resume the original run. Easy-to-read software messages keep users informed of system status.
Sample flexibility with optional walkaway sample loading
Gap-free analysis of intracellular calciumA The three left-hand cytograms show calcium data obtained on a Beckman Coulter CyAn™ ADP using the “stop-flow” method, showing time gaps when control and test compounds were added.
B The three right-hand cytograms show data obtained on a BD Accuri C6, adding the same compounds in open Eppendorf tubes without interrupting sample acquisition. No time gaps were observed; otherwise, both methods obtained comparable data.
Data from Vines A, McBean GJ, Blanco-Fernández A. A flow cytometric method for continu-ous measurement of intracellular Ca2+ concentration. Cytometry Part A. 2010;77:1091-1097; reproduced courtesy of the authors.
A. Beckman Coulter Cyan ADP
A23187
A23187 A23187 A23187ThapsigarginEtOH
A23187 Thapsigargin A23187
B. BD Accuri C6
488:
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/40:
Flu
o-4
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o-4
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A. Beckman Coulter Cyan ADP
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A23187 Thapsigargin A23187
B. BD Accuri C6
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A: Beckman Coulter Cyan ADP
F L U I D I C S
7
Applications in kinetic analysis of cellular responsesChanges to intracellular calcium (Ca2+) levels can occur rapidly, in some cases within nanoseconds of stimulation, and obtaining accurate data is a significant research challenge. To add test compounds to the cell suspension, a “stop-flow” method is often used in which sampling is paused, the sample tube opened, the agonist added, and the tube resealed. This technique leaves a gap in data collection that may miss essential changes in Ca2+ levels.
The BD Accuri C6 employs non-pressurized peristaltic pumps in an open fluidics system. Open tubes allow convenient addition of test compounds to the cell suspension without interrupting sampling. This “continuous-flow” method enables non-stop analysis of calcium flux and other kinetic cellular responses, such as pH, reactive oxygen and nitrogen species, mitochondrial membrane potential, and nanoparticle uptake.
A. Beckman Coulter Cyan ADP
A23187
A23187 A23187 A23187ThapsigarginEtOH
A23187 Thapsigargin A23187
B. BD Accuri C6
488:
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2 min 30 sec 2 min 30 sec 2 min 30 sec 5 minTime
A. Beckman Coulter Cyan ADP
A23187
A23187 A23187 A23187ThapsigarginEtOH
A23187 Thapsigargin A23187
B. BD Accuri C6
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2 min 30 sec 2 min 30 sec 2 min 30 sec 5 minTime
A. Beckman Coulter Cyan ADP
A23187
A23187 A23187 A23187ThapsigarginEtOH
A23187 Thapsigargin A23187
B. BD Accuri C6
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A. Beckman Coulter Cyan ADP
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A23187 A23187 A23187ThapsigarginEtOH
A23187 Thapsigargin A23187
B. BD Accuri C6
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B: BD Accuri C6
Pluripotent stem cell analysis on the BD Accuri C6Frozen fixed H9 embryonic stem cells (hESCs) were stained with antibodies from the BD Stemflow™ Human and Mouse Pluripotent Stem Cell Analysis Kit (Cat. No. 560477) and analyzed on the BD Accuri C6. Compared to isotype controls (not shown), the cells expressed high levels of positive pluripotency markers SSEA-4 and Oct3/4, and low levels of the negative marker SSEA-1.
102
102.
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510
6
103 104 105 106
PerCP-Cy5.5 Oct3-4
D02 05_Ab stainedGate: P1
PE S
SEA
-1
Q1-UL0.2%
Q1-UR1.0%
Q1-LL27.5%
Q1-LR71.4%
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102.
510
410
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Alexa Fluor® 647 SSEA-4
D02 05_Ab stainedGate: P1
PE S
SEA
-1
Q2-UL0.0%
Q2-UR1.5%
Q2-LL0.0%
Q2-LR98.5%
102
102.
710
410
510
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103 104 105 106
Alexa Fluor® 647 SSEA-4
D02 05_Ab stainedGate: P1
PerC
P-C
y5.5
Oct
3-4
Q3-UL0.0%
Q3-UR76.8%
Q3-LL0.0%
Q3-LR23.2%
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BD Accuri C6 software has an intuitive user interface that was developed based on hundreds of hours observing researchers using flow cytometers.
As a result, most novice flow cytometry users find it so easy to use, that they can collect and analyze data in less than an hour. Software options and instrument controls are clearly visible from the software’s tabbed interface which enables access to the collection, analysis, and statistics functions.
Data is acquired from the Collect tab. Users can create new plots, or copy and re-use plots from this tab. The software supports a full range of selection regions including rectan-gular, polygon, quadrant, horizontal, and vertical markers.
The Analyze tab displays plots and samples in any combination. In the Analyze tab, users can create color histogram overlays, print multiple plots, and compare samples. Use the Zoom tool to magnify areas of data, instead of voltage adjustments to set the channel range viewed, to better visualize results.
Sample data can be customized in the Statistics tab. Data is displayed in a master table, and statistics can be easily copied and pasted into spreadsheets to facilitate reporting. To simplify creating presentations, plots can be imported into Microsoft® Office applications using drag and drop. BD Accuri C6 software supports live gating, event coloring, export of publication-quality, vector-scalable graphics, and batch analysis, for review or modification of multiple samples for the automatic creation of Microsoft PowerPoint® and Excel files.
BD Accuri C6 software files can be exported in FCS 3.0 format for seamless importing of user data into flow cytometry analysis programs including FCS Express and FlowJo™.
Intuitive software—master in minutes
Collect tab
S O F T W A R E
9
Analyze tab Batch Analysis tabStatistics tab
Sample figure creation using BD Accuri C6 softwareThe human embryonal carcinoma (EC) cell line 2102Ep can serve as a reference standard for human embryonic and induced pluripotent stem cells because it expresses most of the same markers. After staining with antibodies to stem cell markers, 2102Ep EC cells were collected and analyzed on a BD Accuri C6. Overlays of single-parameter histograms were drawn with BD Accuri C6 software. Plots were dragged and dropped into presentation software, where labels were added.
Gate: (P1 in all)
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Gate: (P1 in all)
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Control
SSEA-4
SSEA-1
Control
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Control
SSEA-4
TRA-1-60
Control
Oct3/4
Gate: (P1 in all)
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Gate: (P1 in all)
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Gate: (P1 in all)
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SSEA-4
SSEA-1
Control
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Oct3/4
Gate: (P1 in all)
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Gate: (P1 in all)
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Gate: (P1 in all)
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Gate: (P1 in all)
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Control
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SSEA-1
Control
TRA-1-60
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Control
Oct3/4
102.8
101.
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4.5
104 105 105.6
FL1-A
Damaged cellsSYBR® Green I+PI+
Intact cellsSYBR® Green I+PI+
P145.0%
FL3-
A
A P P L I C AT I O N S
10
Creating and using software templatesTo make the BD Accuri C6 cytometer even easier to use, software templates are available for BD reagent kits and cocktails. Templates contain a predefined workspace for quick and easy setup and analysis. Markers, regions, gates, parameter names, and sample names are predefined for fast setup.
Templates are available for popular applications such as immunophenotyping, apoptosis, cell cycle, microbial counting, and intracellular cytokines. Users can also develop custom templates for frequently run assays, saving time. Simply open the template, enter settings, and click Run to start immediately collecting data.
Easy to learn and use— fits a wide range of applications
Discriminating intact from damaged bacteria using the Eawag water quality templateA standard flow cytometric staining protocol and a corresponding BD Accuri C6 software analysis template are used to discriminate bac-teria from debris in drinking water samples. When a sample is stained with the DNA dye SYBR® Green I, all bacteria appear within the tem-plate’s single, fixed gate, while noise and debris are excluded. When the sample is co-stained with SYBR® Green I and propidium iodide (PI), damaged bacteria are shifted out of the gate, leaving only viable bacteria within. The template is available at bdbiosciences.com.
Data courtesy of Frederik Hammes, Eawag Department of Environmental Microbiology, Dübendorf, Switzerland.
s o f t w a r e
11
Detection of GFP expression in bacteria Two E. coli cultures, one wild type and the other transfected with a constitutive GFP-expressing plasmid, mixed in a 1:1 ratio.
Data courtesy of Tim F. Cooper, Department of Biology and Biological Chemistry, University of Houston, Houston, TX.
Efficient gene expression analysis Screening thousands of cells for reporter gene expression levels is fundamental to understanding how genes are regulated inside the cell. Advances in flow cytometry and a full spectrum of fluorescent proteins now available allow biomedical researchers to more quickly, easily, and affordably leverage this technology in gene expression analysis.
Fluorescent proteins have come a long way since the original application of Green Fluorescent Protein (GFP) for the detection of gene expression. Fluorescent proteins now span the entire spectrum from short violet to long red, and can be used to study a wide variety of cellular phenomena.
The BD Accuri C6 simplifies the detection of fluorescently tagged genes incorporated into cells. It can also measure the effects of gene knockdown when RNA interference (RNAi) is used to reduce gene expression. With multiparameter flow cytometry, one fluorescent antibody can be used to measure the intracellular level of the transfected siRNA target protein, while others can measure the cells’ functional responses such as up- and downregulation of surface markers or intracellular protein phosphorylation.
E. coli wild type
2000
0 / 1
0000
0 (2
0%)
even
ts d
isp
laye
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SSC
-H
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103.
410
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102 103 104.1
FSC-H
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-H
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0978
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ts d
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ts d
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-H10
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FL1: 530 BP
M10.1%
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ial d
ata
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yed
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P253.0%
100 101 102 103 104 105 106
300
200
100
040
0
FL1: 530 BP
M193.6%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
2,00
01,
000
03,
200
FL1: 530 BP
+ GFP
- GFP
M150.5%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
1,00
050
00
1,60
0
2000
0 / 1
0000
0 (2
0%)
even
ts d
isp
laye
d
SSC
-H
P252.0%
103.
410
310
210
110
0.3
102 103 104.1
FSC-H
P253.0%
SSC
-H
4195
6 / 2
0978
0 (2
0%)
even
ts d
isp
laye
d
103.
410
310
210
110
0.3
102 103 104.1FSC-H
P254.9%
3920
0 / 1
9599
7 (2
0%)
even
ts d
isp
laye
d
SSC
-H10
3.4
103
102
101
100.
3
102 103 104.1
FL1: 530 BP
M10.1%
Part
ial d
ata
dis
pla
yed
Co
un
t
P253.0%
100 101 102 103 104 105 106
300
200
100
040
0
FL1: 530 BP
M193.6%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
2,00
01,
000
03,
200
FL1: 530 BP
+ GFP
- GFP
M150.5%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
1,00
050
00
1,60
0
E. coli + GFP plasmid
2000
0 / 1
0000
0 (2
0%)
even
ts d
isp
laye
d
SSC
-H
P252.0%
103.
410
310
210
110
0.3
102 103 104.1
FSC-H
P253.0%
SSC
-H
4195
6 / 2
0978
0 (2
0%)
even
ts d
isp
laye
d
103.
410
310
210
110
0.3
102 103 104.1FSC-H
P254.9%
3920
0 / 1
9599
7 (2
0%)
even
ts d
isp
laye
d
SSC
-H10
3.4
103
102
101
100.
3
102 103 104.1
FL1: 530 BP
M10.1%
Part
ial d
ata
dis
pla
yed
Co
un
t
P253.0%
100 101 102 103 104 105 106
300
200
100
040
0
FL1: 530 BP
M193.6%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
2,00
01,
000
03,
200
FL1: 530 BP
+ GFP
- GFP
M150.5%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
1,00
050
00
1,60
0
2000
0 / 1
0000
0 (2
0%)
even
ts d
isp
laye
d
SSC
-H
P252.0%
103.
410
310
210
110
0.3
102 103 104.1
FSC-H
P253.0%
SSC
-H
4195
6 / 2
0978
0 (2
0%)
even
ts d
isp
laye
d
103.
410
310
210
110
0.3
102 103 104.1FSC-H
P254.9%
3920
0 / 1
9599
7 (2
0%)
even
ts d
isp
laye
d
SSC
-H10
3.4
103
102
101
100.
3
102 103 104.1
FL1: 530 BP
M10.1%
Part
ial d
ata
dis
pla
yed
Co
un
t
P253.0%
100 101 102 103 104 105 106
300
200
100
040
0
FL1: 530 BP
M193.6%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
2,00
01,
000
03,
200
FL1: 530 BP
+ GFP
- GFP
M150.5%
Co
un
t
Part
ial d
ata
dis
pla
yed
100 101 102 103 104 105 106
1,00
050
00
1,60
0
12
The BD special order program allows customers to purchase instruments configured to fit precise research and assay needs. This innovative program is tailored to the special needs of research at the leading edge of biomedical discovery, and offers a wide range of choices to help researchers create the ultimate customized instrument for their requirements.
To support the evolving needs of researchers, the BD Accuri C6 cytometer can be custom configured by the BD special order team with a wide choice of innovative lasers. This expanded level of flexibility and choice helps make the special order BD Accuri C6 fit a wider choice of research application requirements.
Your BD Sales Representative is your point of contact to discuss a special order product for your lab. Together with an engineer from the special order team, they will follow a structured process to define, design, and manufacture an instrument that exactly matches your requirements. Strict manufacturing controls are in place to ensure high-quality outcomes.
Special order products for unique needs
FL3-
A
FL3-
A
Nu
mb
er o
f N
ucl
ei
FL2-A FL2-A FL2-A
2C
4C
6C
16C
32C
750
500
250
103
105
106
106 104 105104 105
106
105
104
103
102 103 104 105 106
Gated on P1
A B C
P11.8%
R1
Analysis of DNA content and ploidy in plantsArabidopsis thaliana root tissues were chopped with a fresh razor blade, stained with PI, and acquired on the BD Accuri C6. On an FL2 vs FL3 plot, nuclear events cluster in a narrow diagonal region (A, B). Gating on these nuclear events, FL2 fluorescence (C) shows clear peaks corresponding to cell ploidy.
Data courtesy of David W. Galbraith, School of Plant Sciences and Bio5 Institute for Collabora-tive Bioresearch, University of Arizona, Tucson, AZ, USA.
C U S T O M C O N F I G U R AT I O N
13
Phycocyanin fluorescenceFL4 ex: 640; em: 675 ±12.5 nm
Phycocyanin fluorescenceFL4 ex: 640; em: 675 ±12.5 nm
Site 1 Site 2
Site 4Site 3
Ch
loro
ph
yll a
,b f
luo
resc
ence
FL3
ex: 4
88; e
m: 6
70 L
PC
hlo
rop
hyl
l a,b
flu
ore
scen
ceFL
3 ex
: 488
; em
: 670
LP
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
P750.0%
P642.8%
P770.4%
P779.1%
P773.1%
P622.8%
P612.2%
P617.6%
Analysis of aquatic microorganisms with the BD Accuri C6In water samples from four sites in Saginaw Bay, Michigan, plots of phycocyanin fluorescence vs chlorophyll fluorescence were used to separate fluorescent phytoplankton into cyanobacteria (region P6) and other fluorescent phytoplankton (P7). Microorganism counts obtained by direct volume on the BD Accuri C6 showed that sites 1 and 2, close to the nutrient-rich mouth of the Saginaw River, had at least six times more cyanobacteria than the other two locations.
Data courtesy of Juli Dyble Bressie, National Oceanographic and Atmospheric Administration, Seattle, WA, USA.
Speed analysis of marine and freshwater samplesEnvironmental research in marine and freshwater ecosystems is predominantly focused on the microbiomes of those aquatic environments. Of critical concern to environmental research is the primary productivity of phytoplankton and the distribution of phytoplankton and cyanobacteria species responsible for harmful algal blooms.
The BD Accuri C6 can help speed sample analysis for biologists studying marine and freshwater ecosystems. The system is transportable enough to travel aboard ship and can handle particles as small as 0.5 μm, quickly delivering multiparametric measurements of particle size and autofluorescence in both cultures and environmental samples.
Phycocyanin fluorescenceFL4 ex: 640; em: 675 ±12.5 nm
Phycocyanin fluorescenceFL4 ex: 640; em: 675 ±12.5 nm
Site 1 Site 2
Site 4Site 3
Ch
loro
ph
yll a
,b f
luo
resc
ence
FL3
ex: 4
88; e
m: 6
70 L
PC
hlo
rop
hyl
l a,b
flu
ore
scen
ceFL
3 ex
: 488
; em
: 670
LP
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
101 102 103 104 105 106 107.2
107.
210
610
510
410
310
210
1
P750.0%
P642.8%
P770.4%
P779.1%
P773.1%
P622.8%
P612.2%
P617.6%
S E R V I C E S
14
BD Biosciences is fully committed to the success and satisfaction of its customers and offers a range of options for BD Accuri support.
Fast, easy installationThe BD Accuri C6 cytometer can be customer installed within just an hour of taking it out of the box. A step-by-step quick start guide and online video simplify installation.
Preventative maintenance Preventative maintenance procedures should be performed every two months to change the sheath filter, pump tubing, and fluidic filters, and to clean the SIP.
Technical application supportOur technical application support specialists are available to provide field- or phone-based assistance and advice. Expert in a diverse array of topics, technical application specialists are well equipped to address customer needs in both instrument and application support.
Training If desired, optional hands-on training is available on the BD Accuri C6 cytometer. The training combines flow cytometry theory and practical skills to operate the BD Accuri C6 cytometer.
Services and support
BD Biosciences Regional Offices
Office locations are available on our websites.
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