Introduction to

Flow Cytometry
Principles
Data analysis
Protocols
Troubleshooting

By Misha Rahman, Ph.D.

Introduction
to Flow Cytometry
Principles

Data analysis

Protocols

Troubleshooting

By Misha Rahman, Ph.D.

Technical advisors
Andy Lane, Ph.D.
Angie Swindell, M.Sc.
Sarah Bartram, B.Sc.
 Preface
How can I explain what flow cytometry is to someone that knows nothing
about it? Well, imagine it to be a lot like visiting a supermarket. You choose
the goods you want and take them to the cashier. Usually you have to pile
them onto a conveyor. The clerk picks up one item at a time and interrogates
it with a laser to read the barcode. Once identified, and if sense prevails,
similar goods are collected together, e.g. fruit and vegetables go into one
shopping bag and household goods into another. Now picture in your mind
the whole process automated; replace shopping with biological cells; and
substitute the barcode with cellular markers – welcome to the world of flow
cytometry and cell sorting!
We aim to give you a basic overview of all the important facets of flow
cytometry without delving too deeply into the complex mathematics and
physics behind it all. For that there are other books (some recommended at
the back). Instead, we present a guide that will be invaluable to beginners of
flow cytometry, or act as a fact-packed synopsis for those of you interested in
teaching others about the virtues of this powerful application.
At AbD Serotec, we specialize in flow cytometry reagents and offer the
largest range of antibody markers commercially available, together with
accessory buffers. Our guiding principle is to manufacture products for use
with every known flow cytometry instrument. We offer no bias towards any
one machine, but are more interested in maximizing scientific performance.
Confidence in our reagents is shown by our quality promise that states that if
any product does not perform as described on its datasheet, we will replace
the reagent with a fresh vial or offer you credit.
Please visit our website at www.abdserotec.com/flowcytometry for our
ever-increasing range of flow cytometry reagents. You can access detailed
datasheets for every product online. Should you need any further information,
just contact our Technical Services Team (see the back cover for your nearest
office), and they will be happy to assist.
I hope this booklet will prove useful to you. If you like it, let us know and
we’ll produce similar guides for the research applications we support.

Misha Rahman
Marketing Communications Manager

2
Contents
Chapter 1 Principles of the flow cytometer
Fluidics system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Optics and detection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Signal processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Electrostatic cell sorting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

Chapter 2 Principles of fluorescence

Fluorochromes and light . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Maximal absorbance and maximal emission . . . . . . . . . . . . . . . . . . . . 10
Why use a fluorescent probe? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Which fluorochromes are useful for flow cytometry? . . . . . . . . . . . . . . 12
Fluorescence compensation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14

Chapter 3 Data analysis

Gates and regions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Single-parameter histograms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Two-parameter histograms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Intracellular antigens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Immunophenotyping . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

Chapter 4 Common protocols

Sample preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Methods
1  Preparation of cells . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
2  Direct immunofluorescence staining of cells and blood . . . . . . . . . . 26
3  Indirect immunofluorescence staining of cells and blood . . . . . . . . . 27
4  Staining lambda and kappa chains in whole blood . . . . . . . . . . . . . 28
5  Whole blood protocol for analysis of intracellular cytokines . . . . . . 28
6  Direct staining of intracellular antigens . . . . . . . . . . . . . . . . . . . . . . 29
7  Direct staining of intracellular antigens: methanol method . . . . . . . 30

Chapter 5 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31

Recommended reading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33

3
 1

Chapter
Principles of the
flow cytometer

Fluidics system
One of the fundamentals of flow cytometry is the ability to measure the
properties of individual particles. When a sample in solution is injected into
a flow cytometer, the particles are randomly distributed in three-dimensional
space. The sample must therefore be ordered into a stream of single particles
that can be interrogated by the machine’s detection system. This process is
managed by the fluidics system.
Essentially, the fluidics system consists of a central channel/core through
which the sample is injected, enclosed by an outer sheath that contains faster
flowing fluid. As the sheath fluid moves, it creates a massive drag effect on
the narrowing central chamber. This alters the velocity of the central fluid
whose flow front becomes parabolic with greatest velocity at its center
and zero velocity at the wall (see Figure 1). The effect creates a single file
of particles and is called hydrodynamic focusing. Under optimal conditions
(laminar flow) the fluid in the
Central core central chamber will not mix
with the sheath fluid.
The flow characteristics
of the central fluid can be
estimated using Reynolds
Sheath Number (Re):
fluid

Re = pVD
µ

where D = tube diameter,

V = mean velocity of fluid,
Single flow p = density of fluid, and
µ = viscosity of fluid.
When Re < 2300, flow is
always laminar. When Re >
FIGURE 1 Hydrodynamic focusing produces a single 2300, flow can be turbulent,
stream of particles which accelerates diffusion.
4 CH A PT E R 1
 Without hydrodynamic focusing the nozzle of the instrument (typically
70 µM) would become blocked, and it would not be possible to analyze one
cell at a time.

Optics and detection

After hydrodynamic focusing, each particle passes through one or more
beams of light. Light scattering or fluorescence emission (if the particle
is labeled with a fluorochrome) provides information about the particle’s
properties. The laser and the arc lamp are the most commonly used light
sources in modern flow cytometry.
Lasers produce a single wavelength of light (a laser line) at one or more
discreet frequencies (coherent light). Arc lamps tend to be less expensive
than lasers and exploit the color emissions of an ignited gas within a sealed
tube. However, this produces unstable incoherent light of a mixture of
wavelengths, which needs subsequent optical filtering.
Light that is scattered in the forward direction, typically up to 20° offset from
the laser beam’s axis, is collected by a lens known as the forward scatter
channel (FSC). The FSC intensity roughly equates to the particle’s size and can
also be used to distinguish between cellular debris and living cells.
Light measured approximately at a 90° angle to the excitation line is called
side scatter. The side scatter channel (SSC) provides information about the
granular content within a particle. Both FSC and SSC are unique for every
particle, and a combination of the two may be used to differentiate different
cell types in a heterogeneous sample.
Fluorescence measurements taken at different wavelengths can provide
quantitative and qualitative data about fluorochrome-labeled cell surface
receptors or intracellular molecules such as DNA and cytokines.
Flow cytometers use separate fluorescence (FL-) channels to detect light
emitted. The number of detectors will vary according to the machine and its
manufacturer. Detectors are either silicon photodiodes or photomultiplier
tubes (PMTs). Silicon photodiodes are usually used to measure forward
scatter when the signal is strong. PMTs are more sensitive instruments and
are ideal for scatter and fluorescence readings.
The specificity of detection is controlled by optical filters, which block certain
wavelengths while transmitting (passing) others. There are three major filter
types. ‘Long pass’ filters allow through light above a cut-off wavelength,
‘short pass’ permit light below a cut-off wavelength and ‘band pass’ transmit
light within a specified narrow range of wavelengths (termed a band width).
All these filters block light by absorption (Figure 2).

CH A PTER 1 5
 Long pass 500 nm long pass
transmits > 500 nm

Short pass 560 nm short pass

transmits < 560 nm

630/15 nm band pass permits

Band pass everything in the 615–645 nm
band width
Blocked light
absorbed

Dichroic
Light passed
mirror

Blocked light
deflected

Figure 2 Different types of optical filters

When a filter is placed at a 45° angle to the oncoming light it becomes a

dichroic filter/mirror. As the name suggests, this type of filter performs two
functions, first, to pass specified wavelengths in the forward direction and,
second, to deflect blocked light at a 90° angle. To detect multiple signals
simultaneously, the precise choice and order of optical filters will be an
important consideration (refer to Figure 3).

Signal processing
When light hits a photodetector a small current (a few microamperes) is
generated. Its associated voltage has an amplitude proportional to the
total number of light photons received by the detector. This voltage is then
amplified by a series of linear or logarithmic amplifiers, and by analog to
digital convertors (ADCs), into electrical signals large enough (5–10 volts) to
be plotted graphically.
Log amplification is normally used for fluorescence studies because it expands
weak signals and compresses strong signals, resulting in a distribution that is
easy to display on a histogram. Linear scaling is preferable where there is not
such a broad range of signals e.g. in DNA analysis.
The measurement from each detector is referred to as a ‘parameter’ e.g.
forward scatter, side scatter or fluorescence. The data acquired in each
6 CHAPTER 1
 Fluidics system

Filters Detectors
635
nm
FSC

48 8 nm
Lens
Lasers PMT
(FL-1)

PMT
(FL-2)
Filters
PMT
(FL-3)

PMT
(FL-4)

Screen

SSC

Detector

Figure 3 Schematic overview of a typical flow cytometer setup

parameter are known as the ‘events’ and refer to the number of cells
displaying the physical feature or marker of interest.

Electrostatic cell sorting

A major application of flow cytometry is to separate cells according to
subtype or epitope expression for further biological studies. This process is
called cell sorting or FACS™ analysis.
After the sample is hydrodynamically focused, each particle is probed with
a beam of light. The scatter and fluorescence signal is compared to the sort
criteria set on the instrument. If the particle matches the selection criteria,
the fluid stream is charged as it exits the nozzle of the fluidics system.
Electrostatic charging actually occurs at a precise moment called the
‘break-off point’, which describes the instant the droplet containing the
particle of interest separates from the stream.
To prevent the break-off point happening at random distances from the
nozzle and to maintain consistent droplet sizes, the nozzle is vibrated at high
frequency. The droplets eventually pass through a strong electrostatic field,
and are deflected left or right based on their charge (Figure 4).

CH A PTER 1 7
 Laser interrogation

+
Break-off point
(charging)
–

– +
Voltage
+ plates

+ –

Figure 4 Electrostatic flow sorting

The speed of flow sorting depends on several factors including particle size
and the rate of droplet formation. A typical nozzle is between 50–70 µM in
diameter and, depending on the jet velocity from it, can produce
30,000–100,000 droplets per second, which is ideal for accurate sorting.
Higher jet velocities risk the nozzle becoming blocked and will also decrease
the purity of the preparation.

8 CHAPTER 1
Principles of fluorescence
2

Chapter
Fluorochromes and light
Fluorochromes are essentially dyes, which accept light energy (e.g. from
a laser) at a given wavelength and re-emit it at a longer wavelength.
These two processes are called excitation and emission. The process of
emission follows extremely rapidly, commonly in the order of nanoseconds,
and is known as fluorescence. Before considering the different types of
fluorochrome available for flow cytometry, it is necessary to understand the
principles of light absorbance and emission.
Light is a form of electromagnetic energy that travels in waves. These waves
have both frequency and length, the latter of which determines the color of
light. The light that can be visualized by the human eye represents a narrow
wavelength band (380–700 nm) between ultraviolet (UV) and infrared (IR)
radiation (Figure 5). Sunlight, for example, contains UV and IR light that,
although invisible to the eye, can still be felt as warmth on the skin and
measured scientifically using photodetectors. The visible spectrum can further
be subdivided according to color, often remembered by the mnemonic
‘ROY G BV’ standing for red, orange, yellow, green, blue and violet. Red light
is at the longer wavelength end (lower energy) and violet light at the shorter
wavelength end (higher energy).
Higher Lower
energy energy
400 nm 500 nm 600 nm 700 nm

Ultraviolet Infrared

Visible spectrum

Figure 5 The electromagnetic spectrum

Stokes Shift
When light is absorbed by a fluorochrome, its electrons become excited and
move from a resting state (1) to a maximal energy level called the ‘excited
electronic singlet state’ (2). The amount of energy required will differ for each
CH A PTER 2 9
 fluorochrome and is depicted in Figure 6 as Eexcitation. This state only lasts for
1–10 nanoseconds because the fluorochrome undergoes internal
conformational change and, in doing so, releases some of the absorbed
energy as heat. The electrons subsequently fall to a lower, more stable,
energy level called the ‘relaxed electronic singlet state’ (3). As electrons
steadily move back from here to their ground state they release the
remaining energy (Eemission) as fluorescence (4).
As Eemission contains less energy than was originally put into the fluorochrome
it appears as a different color of light to Eexcitation. Therefore, the emission
wavelength of any fluorochrome will always be longer than its excitation
wavelength. The difference between Eexcitation and Eemission is called Stokes
Shift and this wavelength value essentially determines how good a
fluorochrome is for fluorescence studies. After all, it is imperative that the
light produced by emission can be distinguished from the light used for
excitation. This difference is easier to detect when fluorescent molecules have
a large Stokes Shift.

Heat
OUT
2
Excited singlet state

3 Relaxed singlet state

Eexcitation
Eemission
Light
OUT
Light
IN

Ground state
1 4

Figure 6 Stokes Shift

Maximal absorbance and maximal emission

The wavelength of excitation is critical to the total photons of light the
fluorochrome will absorb. FITC (fluorescein isothiocyanate), for example, will
absorb light within the range 400–550 nm but the closer the wavelength is
to 490 nm (its peak or maximum), the greater the absorbance is. In turn, the
more photons absorbed, the more intense the fluorescence emission will be.

10 CHAPTER 2
 Excitation
laser line A B
Peak or Peak or
maximum maximum

Relative fluorescence emission

Relative absorbance

Wavelength (nm) 400 500 600 700 400 500 600 700
Spectrum

Excellent Weak
(blue light) signal signal
(green) (orange)

Figure 7 Light absorbance (left) and light emission (right) of FITC

These optimal conditions are termed maximal absorbance and maximal

emission wavelengths.
Maximal absorbance usually defines the laser spectral line that is used for
excitation. In the case of FITC, its maximum falls within the blue spectrum.
Therefore, the blue Argon-ion laser is commonly used for this fluorochrome,
as it excites at 488 nm, close to FITC’s absorbance peak of 490 nm.
FITC emits fluorescence over the range 475–700 nm peaking at 525 nm,
which falls in the green spectrum. If filters are used to screen out all light
other than that measured at the maximum via channel A (see Figure 7), FITC
will appear green. Hence, ‘fluorescence color’ usually refers to the color of
light a fluorochrome emits at its highest stable excited state. However, if
FITC fluorescence is detected only via channel B (see Figure 7), it will appear
orange and be much weaker in intensity. How the flow cytometer is set up to
measure fluorescence will ultimately determine the color of a fluorochrome.

CH A PTER 2 11
 Why use a fluorescent probe?
The purpose of a fluorescent probe, such as a fluorochrome-conjugated
antibody, is to directly target an epitope of interest and to allow its biological
and biochemical properties to be measured more easily by the flow cytometer.
Fluorescent probes are useful in a wide range of applications including:
identifying and quantifying distinct populations of cells, cell surface receptors
or intracellular organelles; cell sorting; immunophenotyping; calcium influx
experiments; determining nucleic acid content; measuring enzyme activity, and
for apoptosis studies. By changing the excitation light and using more than one
fluorochrome, it is possible to analyze several parameters of the sample at any
one time. This forms the basis of multicolor fluorescence studies.

Which fluorochromes are useful for flow cytometry?

There are dozens of fluorescent molecules (fluorochromes) with a potential
application in flow cytometry. The list is ever growing but it is not the scope of
this booklet to cover them all. Instead, some of the most useful fluorochromes
for surface or intracellular epitope detection are described on page 13. There is
enough variation in the two tables to cover most researchers’ needs.

Single dyes:
Some of these single dyes e.g. FITC have been in use for the past 30 years but
are now facing competition from alternatives like Alexa Fluor® dyes, which
offer the user greater photostability and increased fluorescence.

Tandem dyes:
In a tandem dye, a small fluorochrome takes a ‘piggy-back’ ride on another
larger fluorochrome. When the first dye is excited and reaches its maximal
singlet state, all its energy transfers to the second dye (an acceptor molecule),
located in close proximity. This activates the second fluorochrome, which then
produces the fluorescence emission. The process is called FRET (fluorescence
resonance energy transfer). It is a clever way to achieve higher Stokes Shifts
and, therefore, increase the number of colors that can be analyzed from a
single laser wavelength.
The majority of tandem dyes have been manufactured for the standard 488 nm
laser, which is found in most flow cytometers. Tandem dyes are very useful for
multicolor fluorescence studies especially in combination with single dyes.
For example, Alexa Fluor® 488, Phycoerythrin, PerCP-Cy5.5 and PE-Cy7 can
all be excited at 488 nm, but will produce green, yellow, purple and infrared
emissions respectively, which can be measured using separate detectors.

12 CHAPTER 2
Single Dyes for Flow Cytometry/Microscopy
Fluorochrome Fluorescence Maximal Maximal Spectrally similar dyes
color absorbance (nm) emission (nm)
Alexa Fluor® 405 401 421 Cascade Blue , DyLight® 405
Alexa Fluor® 488 495 519 Cy2, DyLight® 488, FITC
Alexa Fluor® 647 650 665 APC, Cy5, DyLight® 649
Alexa Fluor® 700 Infrared 702 723 Alexa Fluor® 647
APC 650 661 Alexa Fluor® 647, Cy5
Cy5 649 670
DyLight® 405 400 420 Alexa Fluor® 405, Cascade Blue
DyLight® 488 493 518 Alexa Fluor® 488, FITC
DyLight® 549 562 576 Alexa Fluor® 546, Alexa Fluor® 555,
Cy3, TRITC
DyLight® 649 654 673 Alexa Fluor® 647, Cy5
DyLight® 680 692 712 Alexa Fluor® 650, Cy5.5
DyLight® 750 Near Infrared 752 778 Alexa Fluor® 750
DyLight® 800 Infrared 777 794 IR Dye® 800
FITC 490 525 Alexa Fluor® 488, Cy2, DyLight® 488
Pacific Blue™ 410 455
PerCP 490 675
PE 490; 565 578
Texas Red® 596 615
TRITC 596 570 Alexa Fluor® 488, Cy3

Tandem Dyes for Flow Cytometry/Microscopy

Fluorochrome Fluorescence Maximal Maximal Spectrally similar dyes
color absorbance (nm) emission (nm)
APC-Alexa Fluor® 750 Infrared 650 779 APC-Cy7, DyLight® 750
APC-Cy7 Infrared 650 785
PE-Alexa Fluor® 647 496, 546 667
PE-Alexa Fluor® 700 496, 546 723 PE-Cy5, PerCP
PE-Alexa Fluor® 750 Infrared 496, 546 779 PE-Cy7
PE-Cy5 496, 546 667
PE-Cy5.5 496, 546 695
PE-Cy7 Infrared 496, 546 785 PE-Alexa Fluor® 750
Texas Red® 496, 546 615

Abbreviations
APC Allophycocyanin
FITC Fluorescein isothiocyanate
PE Phycoerythrin
PerCP Peridinin-chlorophyll-protein complex

Note. Phycoerythrin (PE) is same as R-Phycoerythrin (RPE).

CH A PTER 2 13
 Fluorescence compensation
One consideration to be aware of when performing multicolor fluorescence
studies is the possibility of spectral overlap. When two or more fluorochromes
are used during a single experiment there is a chance that their emission
profiles will coincide, making measurement of the true fluorescence emitted
by each difficult. This can be avoided by using fluorochromes at very different
ends of the spectrum e.g. Alexa Fluor® 405 and Phycoerythrin; however, this
is not always practical.
Instead, a process called fluorescence compensation is applied during data
analysis, which calculates how much interference (as a %) a fluorochrome
will have in a channel that was not assigned specifically to measure it.
Figure 8 helps to explain the concept.
The graphs show the emission profiles of two imaginary fluorochromes ‘A’
and ‘B’ which are being detected in FL-1 and FL-2 channels respectively.
Because the emission profiles are so close together, a portion of fluorochrome
A spills over into FL-2 (red shade) and conversely, some of fluorochrome B
reaches FL-1 (dark blue shade).
To calculate how much compensation needs to be applied to the dataset if
both dyes are used simultaneously, some control readings must first be taken.
Fluorochrome A should be run through the flow cytometer on its own and the
% of its total emission that is detectable in FL-2 (spillover) determined. The
procedure should be repeated with fluorochrome B, except that this time FL-1
is spillover.
Suppose the results are:

Spillover Fluorescence
FL-1 FL-2
Fluorochrome A N/A 17%
Fluorochrome B 5% N/A

This means that when the two fluorochromes are used for a dual-color
experiment, the true reading for fluorochrome A in FL-1
= (total fluorescence measured in FL-1) minus (5% of fluorochrome B’s total fluorescence)
Similarly, the true reading for fluorochrome B in FL-2
= (total fluorescence measured in FL-2) minus (17% of fluorochrome A’s total fluorescence)
Fortunately, modern flow cytometry analytical software applies fluorescence
compensation mathematics automatically, which simplifies matters
considerably.

14 CHAPTER 2
 FL-1 FL-2

Spectral properties
of two imaginary
fluorochromes,
Fluorescence

'A' and 'B'.

A is measured in
B the FL-1 channel
and B in the FL-2
A channel.

Wavelength

FL-1 FL-2

Spectral overlap.
Dark blue shade represents
the proportion of B
that overlaps into the
Fluorescence

FL-1 channel.
Red shade represents
B the proportion of A
that interferes with
A
FL-2 channel
measurements.

Wavelength

Figure 8 Fluorescence compensation

CH A PTER 2 15
 Data analysis
3

Chapter
Gates and regions
An important principle of flow cytometry data analysis is to selectively
visualize the cells of interest while eliminating results from unwanted
particles e.g. dead cells and debris. This procedure is called gating.

Cells have traditionally been gated according to physical characteristics. For

instance, subcellular debris and clumps can be distinguished from single cells
by size, estimated by forward scatter. Also, dead cells have lower forward
scatter and higher side scatter than living cells. Lysed whole blood cell
analysis is the most common application of gating, and Figure 9 depicts
typical graphs for SSC versus FSC when using large cell numbers. The different
physical properties of granulocytes, monocytes and lymphocytes allow them
to be distinguished from each other and from cellular contaminants.

Density plot Contour diagram

Figure 9 Analysis of lysed whole blood using FSC/SSC

Abbreviations used in histograms: Lin = Linear scale   Log = Logarithmic scale

Log Comp = Logarithmic scale with compensation applied

16 CHAPTER 3
 On the density plot, each dot or point represents an individual cell that has
passed through the instrument. Yellow/green hotspots indicate large numbers
of events resulting from discreet populations of cells. The colors give the
graph a three-dimensional feel. After a little experience, discerning the various
subtypes of blood cells is relatively straightforward.
Contour diagrams are an alternative way to demonstrate the same data.
Joined lines represent similar numbers of cells. The graph takes on the
appearance of a geographical survey map, which, in principle, closely
resembles the density plot. It is a matter of preference but sometimes discreet
populations of cells are easier to visualize on contour diagrams e.g. compare
monocytes in Figure 9.
Newer gating strategies utilize fluorescence parameters along with scatter
parameters. Once again, blood can be used to demonstrate this principle.

Figure 10 Lysed whole blood analysis using scatter and fluorescence

Above on the left is a FSC/SSC plot for human lysed whole blood using
smaller numbers of cells than in Figure 9. The lymphocytes, monocytes and
granulocytes have been gated as region 1 (R1), region 2 (R2) and region
3 (R3), respectively. ‘Region’ simply refers to an area drawn on a plot
displaying flow cytometry data.
On the right the same cells are now plotted as SSC on the y-axis versus CD45
fluorescence on the x-axis. CD45 is a marker expressed on all white blood
cells at varying intensities but is absent on red blood cells. In relative terms,
lymphocytes have a low SSC and high CD45 count (R4), granulocytes have
a high SSC and low CD45 count (R6), while monocytes are somewhere in
between the other two (R5). The major difference between the lymphocytes
CH A PTER 3 17
 gated in R1 and those gated in R4 is the absence of red blood cells in the
latter, making it a much purer preparation. This highlights the usefulness
of gating strategies that combine a scatter parameter with a fluorescence
parameter.

Single-parameter histograms
These are graphs that display a single measurement parameter (relative
fluorescence or light scatter intensity) on the x-axis and the number of events
(cell count) on the y-axis.

Figure 11 A single-parameter histogram

The histogram in Figure 11 looks very basic but is useful for evaluating the
total number of cells in a sample that possess the physical properties selected
for or which express the marker of interest. Cells with the desired
characteristics are known as the positive dataset.
Ideally, flow cytometry will produce a single distinct peak that can be
interpreted as the positive dataset. However, in many situations, flow analysis
is performed on a mixed population of cells resulting in several peaks on
the histogram. In order to identify the positive dataset, flow cytometry should
be repeated in the presence of an appropriate negative isotype control
(see Figure 12).

18 CHAPTER 3
Figure 12 Which is the positive dataset? LEFT, Using rat anti-mouse F4/80 conjugated to
FITC to stain mouse peritoneal macrophages produces two peaks. RIGHT, By running
an appropriate isotype control (rat IgG2b negative control conjugated to FITC) and
overlaying its image on the histogram (blue outline) the positive dataset is identified
as the taller red peak on the right.

Analytical software packages that accompany flow cytometry instruments

make measuring the % of positive-staining cells in histograms easy. For
example, the F4/80 histogram is shown again below with statistics for R2 and
R3 (known on this type of graph as ‘bar regions’).

Figure 13 Statistical analysis

CH A PTER 3 19
 In Figure 13, 99.83% of the negative control (blue outline) is in R2.
28.14% of cells (red shade) ‘stain negative’ for F4/80 (R2) compared to
71.86% in the positive dataset (R3). Additional statistics about the peaks
(median and standard deviation) is also provided automatically here but this
will vary with the software. A similar type of analysis will be generated for
two-parameter histograms.

Two-parameter histograms
These are graphs that display two measurement parameters, one on the
x-axis and one on the y-axis, and the cell count as a density (dot) plot or
contour map. The parameters could be SSC, FSC or fluorescence. Some
examples of two-parameter histograms were illustrated in Figures 9 and 10.
Another example is the dual-color fluorescence histogram presented below.
Lymphocytes were stained with anti-CD3 in the FITC channel (x-axis) and
anti-HLA-DR in the PE channel (y-axis). CD3 and HLA-DR are markers for
T cells and B cells, respectively.

Figure 14 Two-parameter (dual-color fluorescence) histogram

In Figure 14, R2 encompasses the PE-labeled B cells – note their positive

shift along the PE axis. R5 contains the FITC-labeled T cells (positively shifted
along the FITC axis). The top right quadrant contains a few ‘activated T cells’
(about 4% in this sample) that possess some HLA-DR expression also.
As these stain with both antibody markers they are grouped in their own
region (R3). R4 contains cells negative for both FITC and PE (no shift).

20 CHAPTER 3
 Currently, flow cytometry can be performed on samples labeled with up to 17
fluorescence markers simultaneously1. Therefore a single experiment can yield
a large set of data for analysis using various two-parameter histograms.

Intracellular antigens
Staining intracellular antigens like cytokines can be difficult because
antibody-based probes cannot pass sufficiently through the plasma
membrane into the interior of the cell. To improve the situation, cells
should first be fixed in suspension and then permeabilized before adding
the fluorochrome. This allows probes to access intracellular structures while
leaving the morphological scatter characteristics of the cells intact. Many
commercial kits are available today that provide the reagents to carry out
these crucial steps e.g. Leucoperm™ (see Figure 15).

(a) BEFORE

(b) AFTER

Figure 15 Leucoperm™ used in conjunction with an antibody that recognizes MOMA-2, an

intracellular antigen in mouse macrophages and monocytes. After fixation and
permeabilization (b), notice how distinctive the positive dataset becomes.

1Perfetto,
S. et al (2004) Seventeen colour flow cytometry: unravelling the immune system.
Nature Reviews Immunology 4:648–655

CH A PTER 3 21
 Immunophenotyping
All normal cells express a variety of cell surface markers, dependent on the
specific cell type and degree of maturation. However, abnormal growth may
interfere with the natural expression of markers resulting in overexpression
of some and under-representation of others. Flow cytometry can be used
to immunophenotype cells and thereby distinguish between healthy and
diseased cells. It is unsurprising that today immunophenotyping is one of the
major clinical applications of flow cytometry, and is used to aid the diagnosis
of myelomas, lymphomas and leukemias. It can also be used to monitor the
effectiveness of clinical treatments.
The differences between the blood profiles of a healthy individual and one
suffering from leukemia, for instance, are very dramatic. This can be seen
from the FSC v SSC plots in Figure 16. In the healthy person the cell types are
clearly defined, whereas blood from a leukemia patient is abnormal and does
not follow the classic profile.

Normal person Leukemia patient

Figure 16 Immunophenotyping

22 CHAPTER 3
 Testing the patient’s lymphocytes for specific cell surface markers also reveals
more about the condition.

Normal person

CD3 CD20 HLA-DR

Leukemia patient

CD3 CD20 HLA-DR

Figure 17 Diagnosing leukemia

CD3
A normal person has a significant proportion of CD3-positive lymphocytes.
In the patient with leukemia, staining for CD3 is absent.
CD20
In the leukemia patient there are a large number of cells staining positive for
CD20. In the healthy person only a few stain positive.
HLA-DR
The leukemia patient is HLA-DR-positive. In the normal person only a small
number of cells stain positive.
Being CD3-negative, CD20-positive and HLA-DR-positive, a clinician could
diagnose with certainty that this patient is suffering from a B cell lineage
leukemia or lymphoma. The precise classification of disease may be
determined using further antibodies.

CH A PTER 3 23
 Common protocols
4

Chapter
Sample preparation
Single cells must be suspended at a density of 105–107 cells/ml to prevent
the narrow bores of the flow cytometer and its tubing from clogging up.
The concentration also influences the rate of flow sorting, which typically
progresses at 2000–20,000 cells/second. However, higher sort speeds may
decrease the purity of the preparation.
Phosphate buffered saline (PBS) is a common suspension buffer and the most
straightforward samples for flow cytometry include non-adherent cells from
culture, water-borne micro-organisms, bacteria and yeast. Even whole blood
is easy to use – red cells are usually removed by a simple lysis step; it is then
possible to quickly identify lymphocytes, granulocytes and monocytes by their
FSC/SSC characteristics (see page 16).
However, researchers may also wish to analyze cells from solid tissues
e.g. liver or tumors. In order to produce single cells, the solid material must
be disaggregated. This can be done either mechanically or enzymatically.
Mechanical disaggregation is suitable for loosely bound structures
e.g. adherent cells from culture, bone marrow and lymphoid tissue. It involves
passing a suspension of chopped tissue through a fine-gauge needle several
times, followed by grinding and sonication as necessary.
Enzymes are used to disrupt protein-protein interactions and the extracellular
matrix that hold cells together. Their action is dependent on factors including
pH, temperature and co-factors, so care must be taken when choosing
an enzyme. For example, pepsin works optimally between pH 1.5–2.5
but the acidic conditions would damage cells if left unneutralized for too
long, and cell surface antigens of interest may be lost. Chelators like EDTA
and EGTA can remove divalent cations responsible for maintaining cell
function and integrity but their presence may inhibit certain enzymes, for
instance, collagenase requires Ca2+ for activity. Enzymatic and mechanical
disaggregation is often a trial and error process to optimize the isolation of
the epitope under investigation.
To study intracellular components e.g. cytokines by flow cytometry, the
plasma membrane of the cell must be permeabilized to allow dyes or

EDTA   Ethylenediaminetetraacetic acid

EGTA   Ethyleneglycol-bis(2-aminoethylether)-N,N,N’,N’-tetraacetic acid
24 CHAPTER 4
 antibody molecules through while retaining the cell’s overall integrity. Low
concentrations (up to 0.1%) of non-ionic detergents like saponin are suitable.
In summary, the method for sample preparation will depend on the starting
material and the nature of the epitope. Although it is not possible to describe
every eventuality here, some standard protocols are given in this chapter.

1 Preparation of cells
(a) Cells stored in liquid nitrogen
1 Prepare PBS/BSA buffer (phosphate buffered saline pH 7.4 and 1% BSA).
2 Carefully remove cells from liquid nitrogen storage.
3 Thaw rapidly using PBS/BSA buffer and place into a 15 ml conical
centrifuge tube.
4 Centrifuge at 400 g for 5 minutes.
5 Discard supernatant and resuspend pellet in an appropriate amount of
PBS/BSA buffer.
(b) Tissue culture cell lines in suspension
1 Prepare PBS/BSA buffer (phosphate buffered saline pH 7.4 and 1% BSA).
2 Decant cells from tissue culture flask into 15 ml conical centrifuge tube(s).
3 Centrifuge at 400 g for 5 minutes.
4 Discard supernatant and resuspend pellet in 10 ml of PBS/BSA.
5 Centrifuge at 400 g for 5 minutes.
6 Discard supernatant and resuspend pellet in an appropriate amount of
PBS/BSA.
(c) Adherent tissue culture cell lines
1 Prepare PBS/BSA buffer (phosphate buffered saline pH 7.4 and 1% BSA).
2 Harvest cells by gentle scraping using 2 ml of PBS/BSA buffer.
3 Transfer cells to a 15 ml conical tube and add buffer up to 10 ml.
4 Centrifuge at 400 g for 5 minutes.
5 Discard supernatant and resuspend pellet in fresh PBS/BSA (10 ml).
6 Centrifuge at 400 g for 5 minutes.
7 Discard supernatant and resuspend pellet in an appropriate amount of
PBS/BSA buffer.

BSA   Bovine Serum Albumin

CH A PTER 4 25
 (d) Preparing cells from solid/lymphoid tissues
1 Place tissue on a sterile Petri dish. Remove cells by gently perfusing
the tissue using a syringe and needle containing approximately 15 ml
of PBS/BSA (phosphate buffered saline pH 7.4 and 1% BSA).
2 Transfer the cell suspension from the Petri dish into a 15 ml conical
centrifuge tube.
3 Centrifuge at 400 g for 5 minutes.
4 Discard the supernatant and resuspend the pellet in PBS/BSA.
5 Add 10 ml of ammonium chloride lysis buffer.
6 Mix and incubate for 2 minutes. DO NOT EXCEED THIS TIME.
7 Centrifuge at 400 g for 5 minutes.
8 Add 10 ml of PBS/BSA and mix.
9 Centrifuge again at 400 g for 5 minutes.
   10 Discard the supernatant and resuspend the pellet to a final volume of
10 ml with PBS/BSA.
   11 Count cells using a hemocytometer.
   12 Adjust the cell suspension, if necessary, to give a final count of
0.7–1.2 × 107 cells/ml.

2 Direct immunofluorescence staining of cells and blood

This technique is applicable where the fluorochrome is directly linked to the
primary antibody e.g. PE, FITC and Alexa Fluor® conjugates.
Note. Specific methodology for blood appears in [ ] brackets.
  1 Prepare cells appropriately (see section 1). Adjust the cell suspension
to a concentration of 1 × 106 cells/ml with PBS/BSA buffer (phosphate
buffered saline pH 7.4 and 1% BSA).
[ Whole blood samples may be used undiluted unless the cell count is high
e.g. as in leukemia. EDTA and heparin are preferred anti-coagulants].
  2 Aliquot 100 µl of cell suspension [whole blood] into as many test tubes as
required.
  3 Add antibody at the recommended dilution (see specific datasheets).
Mix well and incubate at room temperature for 30 minutes.
  4 Wash cells with 2 ml of PBS/BSA, centrifuge at 400 g for 5 minutes and
discard the resulting supernatant.

26 CHAPTER 4
 [To the blood suspension add freshly prepared red cell lysis buffer e.g. 2 ml
of AbD Serotec’s Erythrolyse and mix well. Incubate for 10 minutes at room
temperature. Centrifuge at 400 g for 5 minutes and discard the supernatant].
Resuspend cells in 0.2 ml of PBS/BSA or with 0.2 ml of 0.5%
paraformaldehyde in PBS/BSA if required.
Acquire data by flow cytometry. Appropriate standards should always be
included e.g. an isotype-matched control sample.

3 Indirect immunofluorescence staining of cells and blood

This technique is applicable where using unconjugated or biotin-conjugated
monoclonal and polyclonal antibodies. A secondary reagent must be used to
visualize the primary antibody e.g. avidin in the case of biotin.
Note. Specific methodology for blood appears in [ ] brackets.
1 Prepare cells appropriately (see section 1). Adjust the cell suspension
to a concentration of 1 × 106 cells/ml with PBS/BSA buffer (phosphate
buffered saline pH 7.4 and 1% BSA).
[ Whole blood samples may be used undiluted unless the cell count is high
e.g. as in leukemia. EDTA and heparin are preferred anti-coagulants].
2 Aliquot 100 µl of cell suspension [whole blood] into as many test tubes as
required.
3 Add primary antibody at the recommended dilution (see specific
datasheets). Mix well and incubate at room temperature for 30 minutes.
4 Add 2 ml of PBS/BSA buffer, centrifuge at 400 g for 5 minutes and discard
the resulting supernatant.
5 Add an appropriate secondary reagent at the recommended dilution
(see specific datasheets). Mix well and incubate at room temperature for
30 minutes.
6 Wash cells with 2 ml of PBS/BSA, centrifuge at 400 g for 5 minutes and
discard the supernatant.
[To the blood suspension add freshly prepared red cell lysis buffer e.g.
2 ml of AbD Serotec’s Erythrolyse and mix well. Incubate for 10 minutes
at room temperature. Centrifuge at 400 g for 5 minutes and discard the
supernatant].
7 Resuspend cells in 0.2 ml of PBS/BSA or with 0.2 ml of 0.5%
paraformaldehyde in PBS/BSA if required.
8 Acquire data by flow cytometry. Appropriate standards should always be
included e.g. an isotype-matched control sample.

AbD Serotec’s Erythrolyse (Product Codes BUF04 B/C)

CH A PTER 4 27
 4 Staining lambda and kappa chains in whole blood
This method should be used with directly-conjugated dual-color reagents
recognizing human kappa and lambda immunoglobulin light chains. 
Detection of immunoglobulin expression specifically on B lymphocytes
requires a procedure to remove blood serum immunoglobulins that would
otherwise cause interference.
1 Collect blood in an anti-coagulant e.g. EDTA, heparin or acid-citrate dextrose.
2 Aliquot 2–3 ml of whole blood into a 25 ml universal container. Then add
20–25 ml of PBS/BSA (phosphate buffered saline pH 7.4 and 1% BSA),
pre-warmed to 37°C, and mix well.
3 Centrifuge at 400 g for 5 minutes. Carefully aspirate the supernatant
taking care not to disturb the cell pellet. Resuspend the pellet in the
residual supernatant.
4 Repeat the wash (steps 2 and 3) twice.
5 Aliquot 100 µl of washed blood into the required number of test tubes.
Add antibody at the recommended dilution (see specific datasheet).
Mix well and incubate at room temperature for 30 minutes.
6 Add a red cell lysis buffer e.g. 2 ml of AbD Serotec’s Erythrolyse and mix
well. Incubate for 10 minutes at room temperature. Centrifuge at 400 g
for 5 minutes and discard the supernatant.
7 Wash cells with 2 ml of PBS/BSA, centrifuge at 400 g for 5 minutes and
discard the supernatant.
8 Resuspend cells in 0.2 ml of PBS/BSA or with 0.2 ml of 0.5%
paraformaldehyde in PBS if required.
9 Acquire data by flow cytometry. Appropriate standards should always be
included e.g. an isotype-matched control sample.

5 Whole blood protocol for analysis of intracellular

cytokines
This is a rapid and simple approach to the analysis of intracellular cytokines
by flow cytometry. It permits the analysis of small samples, and avoids
any possibility of generating artefactual results during the separation of
peripheral blood cells by density gradient centrifugation.

The stimulation conditions described are suitable for IFN gamma, IL-2 and
TNF alpha. Different conditions may be needed for other cytokines.
The procedure requires a reagent kit to fix and permeabilize cells. There are
several available but we recommend Leucoperm™.
28 CHAPTER 4
 Note. All blood samples must be collected into heparin anti-coagulant. EDTA
interferes with the cell stimulation process and, therefore, must be avoided.

1 Aliquot 0.5 ml of blood separately into 2 tubes, then add 0.5 ml of cell
culture medium (without any additives) to each sample.
2 To one tube (the resting population), add monensin to a final
concentration of 3 mM.
3 To the other tube (activated cells), add PMA, ionomycin and monensin to
a final concentration of 10 ng/ml, 2 mM and 3 mM, respectively.
4 Incubate for 2–4 hours at 37°C in a 5% CO2 atmosphere.
5 At the end of the incubation period aliquot 100 µl samples into the
appropriate number of tubes.
6 Add cell surface antibodies at this stage (if needed for your experiment)
and incubate for 15 minutes.
7 Add 100 µl of Leucoperm™ Reagent A per tube and incubate for
15 minutes.  This reagent fixes cells in suspension.
8 Wash twice with PBS containing 0.1% sodium azide and 1% BSA.
9 Add 100 µl of Leucoperm™ Reagent B (permeabilizes cells) and the
required anti-cytokine antibodies.
10 Incubate for 20 minutes.
11 Wash twice using the PBS buffer, and analyze by flow cytometry.

6 Direct staining of intracellular antigens

The detection of intracellular antigens requires a cell permeabilization step
prior to staining. The method described below produces excellent results in
our hands; however other permeabilization techniques have been published,
and may also be successfully used for this application.
1 Harvest cells and determine total number present.
2 Wash twice in wash buffer (PBS containing 1% BSA and 0.1% sodium azide).
3 If required, perform staining of cell surface antigens using appropriate
directly conjugated monoclonal antibodies at this stage. Following
staining, wash cells once in PBS and discard the supernatant.
4 Resuspend cells in Leucoperm™ Reagent A (cell fixation agent) using
100 µl per 1 × 106 cells. Incubate for 15 minutes at room temperature.

Leucoperm™ (Product Codes BUF09, BUF09 B/C)

PMA   Phorbol 12-myristate 13-acetate

CH A PTER 4 29
 5 Wash once in wash buffer.
6 Resuspend cells in Leucoperm™ Reagent B (cell permeabilization agent)
using 50 µl per 1 × 106 cells.
7 Aliquot 50 µl of cell suspension into the required number of tubes
containing directly-conjugated antibodies. Incubate for 30 minutes at
room temperature.
8 Wash once in wash buffer, and then resuspend in 0.25 ml of 0.5%
paraformaldehyde in PBS.
9 Store at 4°C until acquisition on the flow cytometer, preferably within
24 hours.

7 Direct staining of intracellular antigens: methanol method

Methanol modification is particularly suitable for the detection of some
nuclear antigens, such as PCNA and Ki-67.
Note. Phycoerythrin conjugates are not suitable for the detection of
cell surface antigens using this method. 
1 Harvest cells and determine the total number present.
2 Wash twice in wash buffer (PBS containing 1% BSA and 0.1% sodium azide).
3. If required, perform staining of cell surface antigens using appropriate
directly conjugated monoclonal antibodies at this stage. Following
staining, wash cells once in PBS and discard the supernatant.
4 Resuspend cells in cold (2–8°C) Leucoperm™ Reagent A using 100 µl per
1 × 106 cells. Incubate for 10 minutes at 2–8°C.
5 Add 500 µl of cold absolute methanol, vortex and incubate for
10 minutes at 2–8°C.
6. Wash once in wash buffer.
7 Resuspend cells in Leucoperm™ Reagent B using 100 µl per 1 × 106 cells.
8 Aliquot 50 µl of cell suspension into the required number of tubes
containing directly conjugated antibodies. Incubate for 30 minutes at
room temperature.
9 Wash once in wash buffer, and resuspend in 0.25 ml of 0.5%
paraformaldehyde in PBS.
10 Store at 4°C until acquisition on the flow cytometer, preferably within
24 hours.

PCNA   Proliferating Cell Number Antigen

30 CHAPTER 4
Troubleshooting
5

Chapter
If something doesn’t work check through the following list to resolve the
problem. If there are still difficulties and you have purchased an AbD Serotec
antibody our Technical Services Team will be happy to offer further advice.

Problem Course of action

No staining   1 Confirm that all antibodies have been stored correctly according
to the manufacturer’s instructions.
  2 Confirm that commercial antibodies have not exceeded their date
of expiration.
  3 Make sure that appropriate primary or secondary antibodies have
been added.
  4 Make sure that antibody is conjugated to a fluorochrome. If not,
confirm that appropriate fluorochrome-conjugated secondary is
being used.
  5 Confirm that secondary antibody is active – has it been used
successfully with other primary antibodies?
  6 Make sure that correct secondary antibody is being used, which
will recognize your primary antibody.
  7 If the fluorochrome used is Phycoerythrin or Allophycocyanin-
based, make sure that the product has not been frozen.
  8 Is the target antigen present on test tissue? Check literature for
antigen expression and incorporate a positive control of known
antigen expression alongside test material.
  9 Does antibody recognize antigen in test species? Check that
antibody cross-reacts with species being used. Not all antibodies
will cross-react across species.
10 Confirm that correct laser is being used to excite fluorochrome,
and that correct channel is being used to analyze emissions.

PE antibody does not stain   1 PE conjugate may have been frozen. If so, purchase another vial
but same FITC antibody gives of antibody.
good results   2 Paraformaldehyde (PFA) may be a problem. Breakdown of PFA
may release methanol, which will affect staining. Make up fresh
paraformaldehyde. Cells can be analyzed immediately without
fixing.

CH A PTER 5 31


Non-specific staining   1 Non-specific staining may be due to autofluorescence. Solution:

check levels of autofluorescence by including a tube of cells only
(i.e. without any antibody) into your panel.
  2 Certain cells express low affinity Fc receptors CD16/CD32, which
bind whole antibodies via Fc region. For mouse cells, dilute
antibody in SeroBlock FcR (Product Codes BUF041 A/B).
  3 Non-specific staining may be due to the secondary antibody.
Select a secondary antibody that will not cross-react with target
tissue.
  4 Make sure that sufficient washing steps have been included.
  5 Titrate test antibody carefully. Non-specific staining may be
reduced at lower antibody concentrations.

Weak staining   1 Weak staining may be due to overdilution of antibodies. Confirm

that antibodies are used at the correct concentration by titrating
antibodies before use.
  2 Weak staining in indirect staining systems may be due to
prozoning effect, where highly concentrated antibodies may give
weak results. Titrate antibodies carefully.
  3 Weak staining may be due to an excess cell number. Adjust cell
population to recommended density.
  4 Weak staining may be due to the antigen expression. Check
literature for expected levels of expression.
  5 If antigen expression is weak, select an antibody that is
conjugated to a brighter fluorochrome.
  6 Weak staining may be seen if using a cross-reacting antibody
rather than one specific for the target species.
  7 Incubation time and temperature with either primary or
secondary antibody should be optimized.

Unusual scatter profiles   1 Make sure that cells are used as fresh as possible. Profile may be
showing dead cells and debris.
  2 Activation methods may affect scatter characteristics of cells.
  3 If you are using lysing solution, confirm that this is fresh and has
been made up correctly.

Unexpected staining   1 Some reagents may affect certain antigens and, therefore, may
need reviewing e.g. EDTA will affect some platelet markers.
  2 Lysing solutions may affect certain antigens. Select a method
that does not interfere with antigen detection.
  3 Some antigens are expressed intracellularly and, therefore, cell
permeabilization methods may be required. Check manufacturer’s
datasheet for correct permeabilization reagent.

32 CHAPTER 5
Recommended reading
Flow Cytometry: A Practical Approach, 3rd Edition. (Practical Approach Series).
Edited by M.G. Ormerod. Oxford University Press (2000)

Flow Cytometry: Clinical Applications.

Marion G. Macey. Blackwell Scientific Publications, Oxford (1994)

Flow Cytometry: First Principles, 2nd Edition.

Alice L. Givan. Wiley (2002)

The Handbook – A Guide to Fluorescent Probes and

Labeling Technologies, 10th Edition.
Richard P. Haugland. Invitrogen – Molecular Probes (2005)

Immunophenotyping. Carleton C. Stewart and Janet K.A. Nicholson, Editors.

John Wiley & Sons (2000)

Introduction to Flow Cytometry, First Paperback Edition.

James V. Watson. Cambridge University Press. (2004)

Practical Flow Cytometry, 4th Edition.

Howard M. Shapiro. Wiley Liss (2003)

Alexa Fluor® and Pacific Blue™ are trademarks of Molecular Probes Inc., OR, USA
Cy containing products or portions thereof are manufactured under license from Carnegie Mellon
University under U.S. Patent Number 5,268,486 and related patents
Cy® and CyDye® are registered trademarks of GE Healthcare Limited
DyLight® is a registered trademark of Thermo Fisher Scientific and its subsidiaries
FACS™ (Fluorescence Activated Cell Sorter) is a trademark of Becton, Dickinson and Company, CA, USA
IRDye® Infrared Dyes are a registered trademark of LI-COR Biosciences
Leucoperm™ is made for AbD Serotec by AN DER GRUB Bio Research GmbH

33
 Primary and secondary antibodies
Wide range of species, formats, and labels

Accessory products for flow cytometry

, blocking, and calibration
Fluorescence labeling kits and standards

Antibody production and conjugation

From 10 mg to 10 g
Formulated to your specifications

Custom monoclonals in just 8 weeks

Intelligent in vitro screening protocols
“No antibody – No charge” guarantee

www.abdserotec.com/flowcytometry

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Fax: +1 919 878 3751 Email: [email protected]
Email: [email protected]

Worldwide Tel: +44 1865 852 700

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Email: [email protected]

LIT.FLOW.MAY.2014.1 © Bio-Rad Laboratories Inc 2014. All rights reserved. Published by AbD Serotec, A Bio-Rad Company. Endeavour House,
Langford Business Park, Langford Lane, Kidlington, Oxford OX5 1GE, UK.