the detailed study of Immunofluorescence , fluorescent antibody and its application. Especially made for B.Sc, M.Sc and pHD students.
The medical and immunological aspect is covered in this Presentation. For more such presentations please mail: kuldevraj21@gmail.com
2. Lets dive into
basics
• Antibodies are proteins produced by the immune system
in response to infection.
• They are an important part of the body's defence system
as they work to destroy disease-causing organisms (such
as viruses or bacteria) and block them from infecting
human cells.
• These antibodies bind with
antigens ( foreign material entered
in body,which can cause infection)
3. What is
Fluorescence
Fluorescence is a property of a material to
absorb light at one wavelength and emit light of
longer wavelength when it is illuminate by light
The fluorescence can be visualized by
fluorescence microscopy
4. Immunofluorescence
Immunofluorescence is a technique allowing the visualization
of a specific antigen by binding a specific antibody chemically
conjugated with a fluorescent dye such as fluorescein
isothiocyanate (FITC).
Specific antibodies are labeled with a
compound that make them glow when
observed microscopically under
ultraviolet light
6. Direct Immunofluorescence
• Single antibody i.e. primary antibody is used that is
chemically linked to a fluorochrome.
• If the antigen is present, the primary antibody directly
reacts with it and fluorescence can be observed under the
fluorescent microscope
Primary antibody is an
Immunoglobulin(protein) which has affinity
towards antigen
7. Direct Immunofluorescence
• This method uses a single antibody that is
chemically linked to the fluorochrome.
• The antibody recognize the target
molecule ( antigen) and binds to it
• The fluorochrome it carries can be
determined by microscopy
8. 2. FLUOROCHROME
LABELED ANTIBODIES
ARE THEN ADDED TO THE
SLIDE.
• FIXING OF SPECIMEN
(ANTIGEN) INTO THE
SLIDE.
3. INCUBATION AND CAREFUL
WASHING WITH WASH BUFFERS LIKE
PBS TO REMOVE OTHER COMPONENTS
EXCEPT FOR THE COMPLEX OF
ANTIGEN AND FLUOROCHROME-
LABELED ANTIBODY.
4. OBSERVED UNDER A
FLUORESCENCE
MICROSCOPE.
Steps for
visualization
9. Indirect Immunofluorescence
• This technique employs two types of antibodies primary
antibody is not labeled, it binds to the desired antigen
• A secondary antibody, which is labeled with fluorochrome is
added. It has affinity towards primary antibody.
• It binds to the Fc region of primary antibody which has already
combined to the antigen.
• Thus, by using fluorescent microscopy antigen can be detected
10. STEP 1
Fixing of a known
antigen on a slide.
STEP 4
Incubation and
careful washing with
PBS.
STEP 5
Incubation and
careful washing
again with PBS
STEP 2
The specimen to be
tested is applied to the
slide.
STEP 3
A secondary antibody
( fluorescently
labeled) is added.
STEP 6
Observed under the
fluorescence
microscope.
STEP BY STEP FLOWCHART
11. Used in the detection of autoantibodies that cause
auto immune disorders.
1
Significance of Indirect
immunofluorescence
4
3
2 Single fluorochrome-labeled antibody can be used
for detecting many Ag-Ab interactions
Multiple secondary antibodies can bind to the Fc
region of primary antibody which amplifies the
fluorescence signal
More sensitive than direct immunofluorescence test.
12. Applications of
immuno-
fluorescence
used on cell
sections to
determine
presence of
different
biological
molecules
visualization of
cytoskeletons
such as
intermediate
filaments.
diagnosis of
syphilis,
amoebiasis,
leptospirosis,
toxoplasmosis,
and other
diseases.
detection of
rabies virus
antigen in
the skin
smear
to study
distribution of
biological/non
biological
molecules in
tissue
For DNA
labeling
(combination
with non
antibody
method)
detection
and
localization
of a wide
variety of
antigens
7
14. Dyes used for Antibody labeling
Fluorescei
n
Rhodamine AlexaFluor 532-SE
532 nm
573 nm
498 nm
15. Quantification methods
Once the desired antigen is detected using immunofluorescence, following
methods are employed for their quantification
• Flow cytometry
• fluorescence-activated cell sorter (FACS)
