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PCR Troubleshooting Guide

This document provides troubleshooting guidance for common problems that can occur during PCR including no amplicon, low yield, non-specific amplification as smeared or multiple products, bands in negative controls, and reactions that are not reproducible. It lists possible causes for each problem type and recommends actions to address each cause such as optimizing annealing temperature and MgCl2 concentration, checking for primer dimers or inhibitors, increasing template or altering primer concentration.

Uploaded by

Mustafa Khandgawi
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
324 views

PCR Troubleshooting Guide

This document provides troubleshooting guidance for common problems that can occur during PCR including no amplicon, low yield, non-specific amplification as smeared or multiple products, bands in negative controls, and reactions that are not reproducible. It lists possible causes for each problem type and recommends actions to address each cause such as optimizing annealing temperature and MgCl2 concentration, checking for primer dimers or inhibitors, increasing template or altering primer concentration.

Uploaded by

Mustafa Khandgawi
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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PCR Troubleshooting Guide

Problem
No Amplicon

Possible Causes
Error in set up

Error in cycling
Error in gel analysis

Incorrect annealing temperature


Incorrect MgCl2 concentration
Insufficient template
Primer dimers

Primer design error


DNA not clean or contains
inhibitors

Secondary structure in template

Low Yield

Annealing temperature not


optimal
MgCl2 concentration not optimal
Buffer not optimal
Insufficient template
Insufficient primers
Insufficient cycles
Secondary structure in template

GC-rich template

Extension time too short

Long denaturation inactivating


enzyme
DNA not clean or contains
inhibitors

Sample evaporating during


thermal cycling

Actions
Repeat the experiment, checking all reagents
are added in correct volumes. Use master mix to
ensure all components added correctly.
Check program is correct on thermal cycler and
that cycling starts and finishes correctly
Check wells on gel loaded correctly, correct
loading buffer was added to samples, EtBr is
added to gel and UV settings are correct
Run a temperature gradient in 2C increments
Run a MgCl2 gradient of 0.5mM increments
between 1.5 and 4.0mM
Increase template concentration
Increase temperature and/or decrease MgCl2.
Check self complementarity of primers on primer
design software. Redesign primers.
Blast primers. Check primer parameters on
primer design software. Redesign primers
Check template is clean. Check all ethanol was
evaporated from DNA extractions. If inhibitors
are present diluting DNA can improve the
reaction.
Use touchdown PCR, add adjuvant such as
DMSO, BSA or Betaine or use a hot-start Taq
DNA polymerase
Run a temperature gradient in 2C increments
Run a MgCl2 gradient of 0.5mM increments
between 1.5 and 4.0mM
Use a NH4 based buffer instead of KCl based
buffer for greater yield
Increase template concentration
Increase primer concentration
Increase amount of cycles
Use touchdown PCR, add adjuvant such as
DMSO, BSA or Betaine, or use a hot-start Taq
DNA polymerase
Add adjuvant such as DMSO, BSA or Betaine,
or use Thermo-Start DNA Polymerase with High
Performance Buffer.
For long products (>2kb), extension time (in
mins) should be approximately equal to the
number of kb in the amplicon.
Only use a 2 minute denaturation time for
polymerases which do not require a hot-start.
Check template is clean. Check all ethanol was
evaporated from DNA extractions. If inhibitors
are present diluting DNA can improve the
reaction.
Check levels in wells after cycling. Ensure
screw-down lid is pressing firmly on plate. Use
high quality adhesive seals and rigid PCR
plates.

Non-Specific
Amplification
Multiple Products

Priming starting during set up


Annealing temperature not
optimal
MgCl2 concentration not optimal

Overabundance of primer

Run a MgCl2 gradient of 0.5mM increments


between 1.5 and 4.0mM
Use a KCl based buffer instead of a NH4 based
buffer for greater specificity
Blast primers to check specificity. Redesign
primers.
Decrease primer concentration

Overabundance of template

Decrease template concentration

Annealing time too long


Contamination
Priming starting during set up

Decrease time of annealing step


Check no template control (NTC) for bands
Set up reaction on ice or use a hot-start Taq
DNA polymerase
Run a temperature gradient in 2C increments

Buffer not optimal


Primers not specific

Non-Specific
Amplification
Smeared Product

Annealing temperature not


optimal
MgCl2 concentration not optimal
Buffer not optimal
Primers not specific
Overabundance of primer
Overabundance of template
Annealing time too long
Template degraded
Extension time too short

Band in No
Template Control
(NTC) Contamination

Contaminated reagents
Pipettes contaminated
Work area contaminated
Aerosol contamination

Wrong Size Band


Amplified

Contamination
Wrong primers or template added

Different gene form


Reaction Not
Reproducible or
Reaction Stopped
Working

Set up reaction on ice or use a hot-start Taq


DNA polymerase
Run a temperature gradient in 2C increments

Different cycling conditions

dNTPs degraded
Error in set up
Change in component
Inhibitors in template

Run a MgCl2 gradient of 0.5mM increments


between 1.5 and 4.0mM
Use a KCl based buffer instead of a NH4 based
buffer for greater specificity
Blast primers to check specificity. Redesign
primers.
Decrease primer concentration
Decrease template concentration
Decrease time of annealing step
Minimize freeze thawing of DNA. Run template
on agarose gel to check integrity.
For long products (>2kb), extension time (in
mins) should be approximately equal to the
number of kb in the amplicon.
Use a fresh aliquot of reagents
Clean and sterilize pipettes. Use filter tips. Use
different pipettes for pre- and post-PCR.
Clean work bench or move areas. Use a
different area for pre- and post-PCR.
Use a master mix to minimize pipetting steps,
use filter tips, close lids on all tubes and expel
reagents carefully. Change gloves regularly.
Check no template control for bands
Check primers and template vials have been
labeled correctly and selected correctly during
set up.
Check gene for isoforms or splice variants.
Use the same thermal cycler for optimization
and all future experiments. Different cyclers can
vary in ramping speeds and temperature.
dNTPs are very susceptible to freeze thawing.
Replace with a fresh aliquot.
Repeat - checking correct reagents added and
correct thermal cycler program used.
Check any new components that have been
added (eg. new batch of primers)
Decrease template concentration, dilute
template or clean template.

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