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What is Flow Cytometry?
Flow Cytometry uic
Introduction to Flow CytometryIGC Workshop
Multicolor Flow Cytometry
Rui GardnerIGC – April 03, 2013
Adapted from Holden and Trotter (Winter 2006) “Selecting Reagents for Multicolor Flow Cytometry” BD Hotlines newsletter, 11: 31.-34

Outline
• Know Your Instrument• Optical Layout (lasers and filters)
• Choosing the right fluorochromes• Staining Index• Spillover• Compensation• Color Specificities and Tandem Dyes
• Rules for Multicolor Analysis

Know Your Instrument

Know Your Instrument
Reagent Selection starts with Instrument Configuration • Lasers• Detectors and respective filters
Anal
yzer
sCe
ll So
rter
s
FACSCaliburFACScan
MoFloFACSAria
CyAn ADP
HyperCyt
LSR Fortessa

Know Your Instrument (FACScan)
FACScan Optical Configuration
400 450 500 550 600 650 700 750 800
488530/30 585/42 650LP
FL1 FL2 FL3 GFPFITCAlexa488CFSE
PEPICy3
PIPE-Cy5PE-Cy7PerCPPerCP-Cy5.57AADPE-Alexa610
Typical Fluorochromes
488
nm

Know Your Instrument (FACSCalibur)
FACSCalibur Optical Configuration
Typical Fluorochromes
400 450 500 550 600 650 700 750 800
488530/30 585/42 670LP
FL1 FL2 FL3
488
nm63
3 nm
400 450 500 550 600 650 700 750 800
633661/16
FL4APCCy5Alexa647
GFPFITCAlexa488CFSE
PEPICy3
PIPE-Cy5PE-Cy7PerCPPerCP-Cy5.57AADPE-Alexa610

Know Your Instrument (CyAn ADP)
CyAn ADP Optical Configuration
GFPFITCAlexa488CFSE
PEPI
PIPE-Cy5PerCPPerCP-Cy5.5
Typical Fluorochromes
405
nm64
2 nm APC
Cy5Alexa647
400 450 500 550 600 650 700 750 800
488
nm
405450/50
400 450 500 550 600 650 700 750 800
400 450 500 550 600 650 700 750 800
488
642
Alexa 430AmCyanPacific Orange
DAPIAlexa 405Pacific Blue
PIPE-Texas RedPE-Alexa 610
PE-Cy7
APC-Cy7APC-H7Alexa 700*
530/40
530/40 575/25 613/20 680/30 750LP
750LP665/20
FL1 FL2 FL3 FL4 FL5
APC
(FL8
)
APC-
Cy7
(FL9
)
Viol
et 1
(FL6
)
Viol
et 2
(FL7
)

Know Your Instrument (FACSAria)
FACSAria Optical Configuration
GFPFITCAlexa488CFSE
PEPI
PIPE-Cy5PerCPPerCP-Cy5.5
Typical Fluorochromes
407
nm63
3 nm APC
Cy5Alexa647
400 450 500 550 600 650 700 750 800
488
nm
407450/40
DAPI
Alex
a 43
0
400 450 500 550 600 650 700 750 800
FITC PE
PE-T
exas
Red
PerC
P-Cy
5.5
PE-C
y7
400 450 500 550 600 650 700 750 800
APC
APC-
Cy7
488
633
Alexa 430AmCyanPacific Orange
DAPIAlexa 405Pacific Blue
PIPE-Texas RedPE-Alexa 610
PE-Cy7
APC-Cy7APC-H7Alexa 700*
530/30
530/30 585/42 616/23 695/40 780/60
780/60660/20

SSC
FITC
PE
PE-Cy75
#1
#2
#3
#4
#5
#6
#7
#8
#9
Blue
Red
488/
1053
0/40
585/
4061
6/26
95/5BS
555DLP
610DLP
645DLPPE-TxRed
795/50
670/40
APC
Know Your Instrument (MoFlo)
MoFlo Optical Configuration
H-Blue
H-Red
UV
670/30
565 D
CLP
D405/30
Yellow
mCherry
616/26

Know Your Instrument (LSR Fortessa)
LSR Fortessa Optical Configuration
442 nm (BV)
561 nm (YG)488 nm (Blue)

Know Your Instrument (LSR Fortessa)
YELLOW GREEN (561 nm)
YG:561nm
PE-TexasRedPImCherrymRaspberrymplum
630/30 780/60
670/40 590/30
610LP 740LP
650LP
PE-Cy7
630/75 or 590LP in position AFor mCherry detection only
PE-Cy5, PE-A647mPlum
PERFP, DsReddTomatomOrange

Know Your Instrument (LSR Fortessa)
445/15
470/20
577LP
455LP
SSC(BV)
CFP442 nm (BV)
BLUE VIOLET (442 nm)

Know Your Instrument (LSR Fortessa)
BLUE (488 nm)
Blue:488nm
FITCAlexa 488GFPYFP
530/30 780/60
690/40 488/10
502LP 740LP
655LP
PE-Cy7
PE-Cy5
SSC

Know Your Instrument (LSR Fortessa)
Blue:488nm
GFP
510/20 780/60
540/30 488/10
502LP 740LP
525LP
PE-Cy7
YFP
SSC
BLUE (488 nm)
Measure GFP and YFP simultaneously

Choosing The Right Fluorochromes
Adapted from Holden and Trotter (Winter 2006) “Selecting Reagents for Multicolor Flow Cytometry” BD Hotlines newsletter, 11: 31.-34

Rule 1Choose the Brightest Fluorochromes

Fluorochromes (Stain Index)
Brightest Fluorochrome = Highest Stain Index
W2
W1
D
Stain Index (SI) =D/W
MFIPOSITIVE MFINEGATIVEL̶
2 × rSDNEGATIVE
Stain Index =

Fluorochromes (Stain Index)
Freshly isolated lymphocytes, stained with anti-humanCD3 antibodies conjugated with various fluorochromes

Fluorochromes (Choose the brightest)
Reagent Clone Filter Stain Index
PE RPA-T4 585/40 356.3
Alexa 647 RPA-T4 660/20 313.1
APC RPA-T4 660/20 279.2
PE-Cy7 RPA-T4 780/60 278.5
PE-Cy5 RPA-T4 695/40 222.1
PerCP-Cy5.5 Leu-3a 695/40 92.7
PE-Alexa 610 RPA-T4 610/20 80.4
Alexa 488 RPA-T4 530/30 75.4
FITC RPA-T4 530/30 68.9
PerCP Leu-3a 695/40 64.4
APC-Cy7 RPA-T4 7801/60 42.2
Alexa 700 RPA-T4 720/45 39.9
Pacific Blue RPA-T4 440/40 22.5
AmCyan RPA-T4 525/50 20.2
Stain Index of various anti-CD4 fluorochrome conjugates measured on a BD LSR II

Rule 2Minimize Potential Spillover

Spillover (Minimize spillover)
A single fluorochrome can be detected in more than one channel
Spectral Overlap Correcting spillover

A488true = A488measured - % PE true
PE true = PE measured - % A488true0 % 5 % 10 % 15 %20 %30 %
Compensation
Compensation is a mathematical subtraction to correct spectral overlap
http://www.drmr.com/compensation/
1 10 100 1000
1
10
100
1000
1 10 100 1000
1
10
100
1000
1 10 100 1000
1
10
100
1000
1 10 100 1000
1
10
100
1000
1 10 100 1000
1
10
100
1000
Alex
a488
PE
A488true = A488measured - % 1
Roederer, M. 2002. Compensation in Flow Cytometry. Current Protocols in Cytometry. 1.14.1–1.14.20

Spillover (Minimize spillover)
Slide taken from presentation: Mario Roederer, “Compensation: Basic Principles”, Monday, June 20, 2011

Rule 3Reserve brightest fluorochromes for
“dim” antibodies and vice-versa

Colors and Antibody Specificities(Reserve bright labels for dim antibodies)
Single Stain Controls
CD25-PE Fluorescence
CD25-PE Fluorescence
CD4-
Alex
a488
Flu
ores
cenc
eCD
4-Al
exa4
88 F
luor
esce
nce
CD4-
PE F
luor
esce
nce
CD4-
PE F
luor
esce
nce
CD25-Alexa488 Fluorescence
Single Stain Controls
CD25-Alexa488 Fluorescence

Rule 4Avoid spillover from bright populations into detectors requiring high sensitivity

Sample
CD25-PE Fluorescence
CD4-
Alex
a488
Flu
ores
cenc
e
Single Stain Controls
CD4-
Alex
a488
Flu
ores
cenc
eCD
4-Al
exa4
88 F
luor
esce
nce
CD25-PE Fluorescence
CD25-PE Fluorescence
Colors and Antibody Specificities(Avoid spillover of bright cells into detectors of dim signals)
CD4-
Cy5
Fluo
resc
ence
CD4-
Cy5
Fluo
resc
ence
CD25-PE Fluorescence CD25-PE Fluorescence

Rule 5Take steps to avoid tandem dye degradation

Tandem Dyes
Watch out for degradation
APC Fluorescence APC Fluorescence APC Fluorescence
PE-C
y5 F
luor
esce
nce
PE-C
y5 F
luor
esce
nce
PE-C
y5 F
luor
esce
nce
TIME
PE-Cy5PE-Cy7 APC-Cy7 APC-H7
APC- 30% PE-Cy5 APC- 40% PE-Cy5 APC-50% PE-Cy5

“Rules” for selecting Multicolor Paneltaken from BD Biosciences
Rule 1: Choose the brightest set of fluorochromes for your particular instrument configuration.
Rule 2: Choose fluorochromes so as to minimize the potential for spillover.
Rule 3: Reserve the brightest fluorochromes for “dim” antibodies, and vice versa.
Rule 4: Avoid spillover from bright cell populations into detectors requiring high sensitivity for those populations.
Rule 5: Take steps to avoid tandem dye degradation, and consider its impact upon results.

Recommended Multicor Panel
5-color 6-color 8-color 10-color
FITC or Alexa 488 FITC or Alexa 488 FITC or Alexa 488 FITC or Alexa 488
PE PE PE PE
PE-Texas Red or PE-Alexa 610
PerCP-Cy5.5 PerCP-Cy5.5 PerCP-Cy5.5 PerCP-Cy5.5
PE-Cy7 PE-Cy7 PE-Cy7 PE-Cy7
APC , Alexa 647 or Cy5 APC , Alexa 647 or Cy5 APC , Alexa 647 or Cy5 APC , Alexa 647 or Cy5
Alexa 700
APC-Cy7 APC-Cy7 APC-Cy7
AmCyan AmCyan
Pacific Blue Pacific Blue
Fluorochrome choices for 5 or more colors (Recommended by BD)

Recommended Multicor Panel
5-color 6-color 8-color 10-color
FITC or Alexa 488 FITC or Alexa 488 FITC or Alexa 488 FITC or Alexa 488
PE PE PE PE
PE-Texas Red or PE-Alexa 610
PerCP-Cy5.5 or PerCP PerCP-Cy5.5 or PerCP PerCP-Cy5.5 or PerCP PerCP-Cy5.5 or PerCP
PE-Cy7 PE-Cy7 PE-Cy7
APC , Alexa 647 or Cy5 APC , Alexa 647 or Cy5 APC , Alexa 647 or Cy5 APC , Alexa 647 or Cy5
Alexa 700
APC-Cy7 APC-Cy7
Pacific Orange Pacific Orange
Pacific Blue Pacific Blue Pacific Blue Pacific Blue
Fluorochrome choices for 5 or more colors (Recommended by IGC)
Completely Outdated!

What is Flow Cytometry?
Flow Cytometry uic
Introduction to Flow CytometryIGC Workshop
Multicolor Flow Cytometry (end)
Rui GardnerIGC – Aprli 03, 2013