Emulsion pcr

9,648 views 11 slides May 16, 2018
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About This Presentation

Emulsion PCR
One the basic technique of NGS


Slide Content

Emulsion Polymerase Chain
Reaction
Presented by:
Salman Jamil
(2014-bte-012)
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What is Emulsion PCR?
“Emulsion PCR is a PCR variation
that some NGS technologies use to
replicate DNA sequences.
It is conducted on a bead surface
within tiny water bubbles floating on
an oil solution.”
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Principle
The basic principle of ePCR is dilution and
compartmentalization of template molecules in water
droplets in a water-in-oil emulsion.
Each droplet contains a single template molecule and
functions as a micro-PCR reactor.

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Procedure
Fragmentation of DNA
•The sample is fragmented ranging from 300 to
800bp.
Ligation of adapters
•Adapters with one end sticky and one blunt are ligated
with fragments.
•Phosphates are removed from sticky ends to avoid
dimerization.
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Procedure
Formation of clonal bead populations
•Beads coated with
streptavidin are used.
•Beads have primers that
matches the adapters used.
•Each bead is emulsified in a water-in-oil droplet with
PCR reagents (DNA polymerase, primers, buffers,
dNTPs).
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Formation of clonal bead
populations
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Amplification
Denaturation to single strands
•The double stranded DNA's with adapters are
then denatured by heating the DNA up to 95 °C.
Annealing of ssDNA
•The ssDNA is then attached to the beads.
•Reverse strand (bottom strand or 3’-5’ strand) anneal
to the f-primer on bead surface and r-primer anneal
to the forward strand (top strand or 5’-3’ strand)


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Amplification
Extension
•Polymerase amplifies the forward strand (5’-3’)
starting from beads towards the primer site.
•The reverse strand is amplified starting from primer
towards the bead site.
 Cycle
•Each newly formed double-strand is denatured,
allowing for the strand to ligate to another site on the
surface of the bead. Eventually, 1 million copies of
the target is amplified on the surface of each bead.
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Procedure
Emulsion Breaking
•After amplification, the emulsions are broken using
isopropanol and detergent buffer. The solution is
then vortexed, centrifuged, and magnetically
separated.

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