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1. Serologic techniques

2. Learning Objective
The students should be able to:
1. List material and equipment for serological tests
2. Collect, preserve and prepare serological specimens
3. Run complement inactivation procedure and state
its importance
4. Run serial dilution, determine end point and titer.

3. Outline
1. Introduction
2. Materials necessary for basic serologic tests
3. Collection, preparation and preservation of
serologic al tests
4. Shipment of serological specimens
5. Complement inactivation
6. Dilution and Serial dilution

4. 1. Introduction
 Dilution is the act of making a weaker solution
from a strong solution.
 Serial dilution The systematic re-dilution of a
fluid number of times is called a Serial dilution
 Titer is the reciprocal of the highest dilution
showing a positive reaction
 Complement is a group of non-immunoglobulin
plasma proteins that are sequentially activated by
Ag–Ab complexes

5. Types of glassware include:
 Test tubes
 Glass slides
 Serological pipette with a size of 10ml, 5ml, 2ml
and 1ml.
2. Materials necessary for basic
serologic tests

6. 2. Materials necessary for basic
serologic tests
Glassware
 Dirty glassware easily affects serological tests.
 After using all the glassware (test tube, beaker,
pipette, etc) they should be soaked in detergent
for several hours and rinsed several times in tap
water.
 Finally, allow drying by placing in a dry oven or
dust free place. Test tubes and pipettes should
not be scratched or broken, which will interfere
with the reading of a test.

7. Glassware's and plastic wares

8. Constant Temperature Device
 Incubators and water baths are used in
serological tests. These materials are
electrically operated and have thermostat that
hold the temperature within the required
limits. These devices should be checked prior
to use by a thermometer.
2. Materials necessary for basic
serologic tests

9. Rotating Machine
 Rotating machines are required to facilitate
antigen antibody reactions. Such machines have
a flat plate, which rotate at a prescribed rate of
speed. A knob located on the front of the
machine controls the number of revolutions per
minute.
2. Materials necessary for basic
serologic tests

11. 3. Collection, Preparation And
Preservation Of Specimens
For Serologic tests
A.Types of Specimens
 Specimens that are used for serologic test
include: serum, plasma and cerebrospinal
fluid.
 Serum or plasma samples could be obtained from
venous blood, which can be collected by the
laboratory personnel.
 CSF should be collected by a physician or

12. B. Serum or plasma sample collection
 Collect 2-3ml of venous blood from a patient
using a sterile syringe and needle.
 If serum is required, allow the whole blood to clot
at room temperature for at least one hour,
 Centrifuge the clotted blood for 10 minutes at
2000 rpm.
3. Collection, Preparation And
Preservation Of Specimens
For Serologic tests

13. B. Serum or plasma sample collection
 Transfer the serum to a labeled tube with a
paster pipette and rubber bulb.
 Plasma samples are obtained by treating fresh
blood with anticoagulant,
 Centrifuge and separate the supernatant.
3. Collection, Preparation And
Preservation Of Specimens
For Serologic tests

14. B. Serum or plasma sample collection
 The specimen should be free from hemolyzed blood.
 Finally, seal the specimen containing tube; the tube
should be labeled with full patient's identification
(age, sex, code number, etc).
 The test should be performed within hours after
sample collection, if this could not be done preserve
it at -20oc.
2. Collection, Preparation And
Preservation Of Specimens
For Serologic tests

15.  Most health center and clinic laboratories are
limited in the diagnostic procedures that can be
carried out and have to ship serologic specimens
to other laboratories.
 Before shipment, the following things should be
considered.
 Don't ship whole blood unless the tests to be
performed require whole blood.
 Don't inactivate serum or plasma.
4. Shipment of serological
specimens

16. Serum, plasma, and CSF should be handled as
follows:
 Collect and process specimens under sterile
conditions.
 Ship specimens by the fastest route as soon after
collection as possible.
 Don't ship whole blood unless the test to be performed
required whole blood.
 Remove cells from plasma and clot from serum before
shipment.
4. Shipment of serological
specimens

17. Serum, plasma, and CSF should be handled as
follows:
 Don't inactivate serum or plasma before mailing.
 Keep the specimen and packing container in the
refrigerator until time of shipment.
 Shipment is requires several days preserve by
refrigeration in transit. First, freeze the
specimen; then pack and ship in a well-insulated
container with dry ice.
4. Shipment of serological
specimens

18.  Complement is a group of non-immunoglobulin
plasma proteins that are sequentially activated
by Ag–Ab complexes (or directly by microbial
constituents) and cause irreversible damage to
membrane of cellular target
5. Complement inactivation

19.  Some tests need inactivated serum. Others do
not.
 Inactivation may be important since complement
promotes lysis of erythrocytes and can contribute
to false test results in tests using RBCs.
 Some complement components may also cause
false agglutination in some tests.
5. Complement inactivation

20.  Complement components can be inactivated by
of three mechanism
 Spontaneous decay
 Enzymatic degradation of C4, C3 and C5
rapidly decay
 Stoichiometric inhibition
5. Complement inactivation

21.  The complement in serum must be inactivated
usually by stoichiometric inhibition for most
serological testing.
 To inactivate complement, place tubes of serum
in hot water bath (56c) for 30min
 If the protein complement is not inactivated it will
promote lysis of the red cells and other types of
cells and can therefore produce invalid results
5. Complement inactivation

22.  Complement is also known to interfere with
certain tests for syphilis.
 Serum samples to be tested more than 4 hours
after inactivation should be reheated at 560c for
10 minutes and allowed to cool to room
temperature
5. Complement inactivation

23.  Dilution is the act of making a weaker solution
from a strong solution.
 Adding a diluent such as water or saline,
which contains none of the material being
diluted, is used to do this.
6. Dilution

24. Dilution techniques
 Dilutions can be used in the laboratory to change
the concentration of the body fluids, such as serum
so that it is consistent with the range of an assay.
 Making dilutions can also be necessary to prepare
reagents and standards.
 Dilution has two parts: diluents and solute.
6. Dilution

25.  A dilution involves adding of a substance, the
diluent to other substances, the solute.
 Dilutions show the relative amount of the solute
in the dilute solution.
 It is an indicator of concentration, not volume.
6. Dilution

26.  For a 1:10 dilution, the dilution factor is 10. For a :
b dilution the dilution factor is b.
6. Dilution

27. Technique
 Two liquids of very different compositions (density,
or surface tension) is required
 An exact volume of concentrated solute is added to
a calibrated flask or container, and then diluent is
added to the required volume.
 Adequate mixing must take place to ensure
homogeneity
6. Dilution

28. E.g.,
if you want to prepare 1:10 dilution
 Take 1 ml solute
 Take 9 ml solvent
 Then mix
1st
2nd
6. Dilution

29.  When a solution is diluted with water, its
concentration is decreased and its volume is
increased. But the total amount of solute remains
constant.
 Mathematical expressions of the dilutions are;
CiVi = CfVf Where, Ci is initial concentration
Vi is initial volume.
Cf final concentration
Vf is final volume.
6. Dilution

30. Serial dilutions
 Serial dilutions are a unique type of dilution
techniques.
 In serial dilution, all dilutions, except the 1st are
prepared from the previous dilution and all
dilutions made after the initial dilution are the
same.
6. Dilution

31.  Serial dilutions are used to prepare sets of
standard solutions and are also used to
prepare patient's samples to analyze
components that can exist over a wide
concentration range, such as antibody titers.
6. Dilution

32. 0.1 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5
0.5 0.5
initial
Tube 1 2 3 4 5 6 7 8 9 10
Dilution 1:10 1:20 1:40 1:80 1:160 1:320 1:640 1:1280 1:2560 1:5120
Dilution
factor 10 20 40 80 160 320 640 1280 2560 5120
0.5
0.9 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0.5
6. Dilution

33. An example of the serial dilution is as follows: -
 Into each of ten test tubes is measured 0.5 ml of
saline 1/2 ml of serum is placed in the 1st tube and
mixed.
 Since there is 0.5 ml of serum in a total volume of
1.0 ml; a 0.5:1 or a 1:2 dilution exists in the first
tube.
6. Dilution

34.  Now, 0.5 ml of this solution is removed and mixed
with the 0.5 ml of saline in the 2nd tube; this gives
another 1:2 dilution, but since the 0.5 ml of solution
put into the 2nd tube is already a 1:2 dilution of the
serum, the dilution of serum in the 2nd tube is one
half that of the 1st tube or 1/2 of ½ =1/4 or 1:4.
 This and, by applying the above reasoning, the
dilutions of serum are found to be (1/2)10 = 1/1024
or 1: 1024 in the 10th tube.
6. Dilution

35. Try the following problems
 For ASO titer, tube 1 contains 0.8ml 0f saline,
tubes 2 to 5 contain 0.5ml of saline; 0.2ml of
serum is added to tube 1, and serial dilutions
using 0.5ml are carried out in the remaining
tubes. What is the dilution in each tube?
 Explain the shipment of specimen and
complement inactivation.
Review questions

36. Reference
1. Tizard. Immunology an introduction,4th edition
,Saunders publishing,1994
2. Naville J. Bryant Laboratory Immunology and
Serology 3rd edition. Serological services
Ltd.Toronto,Ontario,Canada,1992
3. Mary Louise .Immunology and Serology in
Laboratory medicine 3rd edition