3.3 Microarrays 39
Action/ExplanationComponents Cycle
Heat together to
95°C:
Ds DNA, Primer and
heat-stable Taq
polymerase
Double-stranded
DNA separates at
95°C:
Strands separate
Cool to 54°C:
Primer has bases
complementary to
some on ss DNA;
hence anneals with
ss DNA
Heat to 75°C,
optimum temp for
Taq polymerase:
Taq polymerase
becomes active and
ss DNA extends and
ds DNA forms
ss DNA becomes ds
DNA
ie quantity of DNA
now double
F I R S T C Y C L E
Ds
DNA
Primer Taq polymrase
SS
DNA
SS
DNA
All three continue
to be heated
together to 95°C in
second cycle:
Ds DNA, Primer and
heat-stable Taq
polymerase
New double-
stranded DNA
separates at 95°C:
Strands separate
Cool to 54°C:
Primer has bases
complementary to
some on ss DNA;
hence anneals with
ss DNA
Heat to 75°C,
optimum temp for
Taq polymerase:
Taq polymerase
becomes active and
each of the two ss
DNA extends and
four ds DNA form
ss DNA becomes
ds DNA
ie quantity of DNA
now double,
become 4 times in
second cycle
S E C O N D C Y C L E
Fig. 3.4 Diagrammatic representation of PCR