Blotting Techniques

BLOTTING TECHNIQUES
By:
A.ADAIKALA ARUL
RAJANATHAN
e-mail : rajanathan027@gmail.com
• Professor Sir Edwin
Southern, Professor of
Biochemistry and Fellow of
Trinity developed this
method in 1975.
• Southern won the Lasker
Award for Clinical Medical
Research prize for the
method of finding specific
DNA sequences he
Professor Sir Edwin developed more than 30
Southern years ago. The technique is
known as DNA transfer or
'Southern blotting'
What is blotting?
• Blots are techniques for transferring DNA ,
RNA and proteins onto a carrier so they
can be separated, and often follows the
use of a gel electrophoresis. The Southern
blot is used for transferring DNA, the
Northern blot for RNA and the western blot
for PROTEIN.
TYPES OF BLOTTING
TECHNIQUES
Blotting technique
Southern Blot Northern Blot Western blot

It is used to detect DNA. It is used to detect RNA. It is used to detect protein.
Blotting sheet
• Whatman 3MM paper is
the world’s most widely
used blotting paper. This
acceptance and usage is
due to the high quality,
purity and consistency that
are relied upon by
researchers doing
Southern, Northern and
Western transfers.
• 3MM paper is now available
in the most widely used
sizes. A medium thickness
paper (0.34 mm) is used
extensively in
electrophoresis for lifting
of sequencing gels.
Creating the Sandwich
The sandwich consists of :

filter paper
Nitrocellulose membrane,
gel matrix
another piece
of filter paper
Cont……
• Cut two pieces of filter paper and a piece of
nitrocellulose membrane to an appropriate size, and
soak them in transfer buffer..
• Place a piece of buffer soaked filter paper over the
gel.
• Flip the gel over, Place the buffer soaked
nitrocellulose membrane against the exposed gel.
• Place the second piece of buffer soaked filter
paper on the nitrocellulose membrane (covering it)
• Check to see that there are no bubbles between
the membrane and the gel.
SOUTHERN BLOTTING
• This method Involves separation,
transfer and hybridization.
• The Southern blot is used to detect the
presence of a particular piece of DNA in
a sample.
• The DNA detected can be a single gene,
or it can be part of a larger piece of
DNA such as a viral genome.
• The key to this method is Hybridization.
• Hybridization - Process of forming a
double-stranded DNA molecule between
a single-stranded DNA probe and a
single-stranded target patient DNA.
PRINCIPLE
1. The mixture of molecules is separated.
2. The molecules are immobilized on a matrix.
3. The probe is added to the matrix to bind to
the molecules.
4. Any unbound probes are then removed.
5. The place where the probe is connected
corresponds to the location of the immobilized
target molecule.
APPARATUS
Steps in southern blotting
1.The DNA to be analyzed,
such as the total DNA of
an organism, is digested
to completion with a
restriction enzyme.
2.The complex mixture of

fragments is subjected to
gel electrophoresis to
separate the fragments
according to size.
CONT…….
3.The restriction fragments

present in the gel are
denatured with alkali and
transferred onto a
nitrocellulose filter or nylon
membrane by blotting.
 This procedure preserves

the distribution of the
fragments in the gel,
creating a replica of the gel
on the filter.
CONT…….
4. The filter is incubated
under hybridization
conditions with a
specific radiolabeled
DNA probe.
 The probe hybridizes to
the complementary DNA
restriction fragment.
CONT…….
 5. Excess probe is
washed away and the
probe bound to the
filter is detected by
autoradiography,
which reveals the
DNA fragment to
which the probe
hybridized.
An Example
APPLICATIONS
• Southern blots are used in gene discovery ,

mapping, evolution and development studies,
diagnostics and forensics.
• In regards to genetically modified organisms,
Southern blotting is used for testing to
ensure that a particular section of DNA of
known genetic sequence has been successfully
incorporated into the genome of the host
organism.
APPLICATIONS
• Southern blots allow investigators to
determine the molecular weight of a
restriction fragment and to measure relative
amounts in different samples.
• Southern blot is used to detect the presence
of a particular bit of DNA in a sample
• analyze the genetic patterns which appear in a
person's DNA.
• analyze restriction digestion fragmentation of
DNA or a biological sample
Northern Blotting
• Northern blotting is a technique for
detection of specific RNA sequences.
Northern blotting was developed by
James Alwine and George Stark at
Stanford University and was named
such by analogy to Southern blotting.
Steps involved in Northern blotting
1. RNA is isolated from
several biological
samples (e.g. various
tissues, various
developmental stages of
same tissue etc.)
* RNA is more
susceptible to
degradation than DNA.
CONT…….
2. Sample’s are loaded

on gel and the RNA
samples are separated
according to their size
on an agarose gel .
 The resulting gel

following after the
electrophoresis run.
CONT…….
3. The gel is then

blotted on a nylon
membrane or a
nitrocellulose filter
paper by creating the
sandwich
arrangement.
CONT…….
4. The membrane is placed

in a dish containing
hybridization buffer
with a labeled probe.
 Thus, it will hybridize to
the RNA on the blot
that corresponds to the
sequence of interest.
5. The membrane is washed

to remove unbound
probe.
CONT…….
6. The labeled probe is

detected via
autoradiography or via a
chemiluminescence
reaction (if a chemically
labeled probe is used).
In both cases this
results in the formation
of a dark band on an X-
ray film.
 Now the expression

patterns of the sequence
of interest in the
different samples can be
compared.
APPLICATIONS
• A standard for the direct study of gene
expression at the level of mRNA (messenger RNA
transcripts).
• Detection of mRNA transcript size
• Study RNA degradation
• Study RNA splicing - can detect alternatively
spliced transcripts
• Study RNA half-life
• Study IRES (internal ribosomal entry site) - to
remove possibility of RNA digestion vs. 2nd cistron
translation.
• Often used to confirm and check transgenic /
knockout mice (animals)
Disadvantages of Northern
Blotting
• Often radioactivity is used. This prevents ease
of performing it, use and disposal. New
methods of non-radioactive detection have
been generated allowing non-radioactive
detection.
• The whole process of northern blotting takes a
long time usually, from sample preparation
through to detection.
• If RNA samples are even slightly degraded by
RNases, the quality of the data and
quantitation of expression is quite negatively
affected.
Cont.....
• The standard northern blot method is
relatively less sensitive than nuclease
protection assays and RT-PCR. The sensitivity
of northern blots may be increased with the
use of nylon positively-charged membranes,
use of a highly specific antisense probe.
• Detection with multiple probes is a problem.
Often, the membranes must be stripped
before hybridization and detection with a
second probe. This is a problem as harsh
conditions are required to strip off probes
from the blot and is also time consuming. Also,
there is a limit to the amount of times a blot
may be stripped.
Western blotting
• Western blotting is an Immunoblotting
technique which rely on the specificity of
binding between a molecule of interest and a
probe to allow detection of the molecule of
interest in a mixture of many other similar
molecules.
• In Western blotting, the molecule of interest
is a protein and the probe is typically an
antibody raised against that particular
protein.
• The SDS PAGE technique is a prerequisite for
Western blotting .
Steps in western blotting
• A protein sample is
subjected to
electrophoresis on
an SDS-
polyacrylamide gel.
• Electroblotting
transfers the
separated proteins
from the gel to the
surface of a
nitrocellulose
membrane.
3. The blot is incubated with a
generic protein (such as milk
proteins or BSA) which binds
to any remaining sticky places
on the nitrocellulose.
4. An antibody that is specific
for the protein of interest
(the primary antibody - Ab1) is
added to the nitrocellulose
sheet and reacts with the
antigen. Only the band
containing the protein of
interest binds the antibody,
forming a layer of antibody
molecules .
5. Following several rinses
for removal of non-
specifically bound Ab1, the
Ab1-antigen complex on
the nitrocellulose sheet is
incubated with a second
antibody (Ab2), which
specifically recognizes the
Fc domain of the primary
antibody and binds it. Ab2
is radioactively labeled, or
is covalently linked to a
reporter enzyme, which
allows to visualize the
protein-Ab1-Ab2 complex.
Applications
• The confirmatory HIV test employs a Western
blot to detect anti-HIV antibody in a human serum
sample. Proteins from known HIV-infected cells
are separated and blotted on a membrane then,
the serum to be tested is applied in the primary
antibody incubation step; free antibody is washed
away, and a secondary anti-human antibody linked
to an enzyme signal is added. The stained bands
then indicate the proteins to which the patient's
serum contains antibody.
• A Western blot is also used as the definitive test
for Bovine spongiform encephalopathy (BSE,
commonly referred to as 'mad cow disease').
• Some forms of Lyme disease testing employ
Western blotting.
DISCUSSION
• http://www.molecularstation.com/dna/southern-
blot/
• http://www.bio.davidson.edu/COURSES/GENOMICS/
method/Southernblot.html
• http://www.med.unc.edu/pmbb/MBT2000/Northern%2
0Blotting.htm
• http://www.bme.gatech.edu/vcl/WesternBlotting/Bac
kground/Introduction.htm
• http://www.bio.davidson.edu/COURSES/GENOMICS/
method/westernblot.html
• http://teachline.ls.huji.ac.il/72320/methods-
tutorial/western/western-blot.html

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BLOTTING TECHNIQUES

Southern Blot Northern Blot Western blot

The sandwich consists of :

2.The complex mixture of

3.The restriction fragments

 This procedure preserves

• Southern blots are used in gene discovery ,

2. Sample’s are loaded

 The resulting gel

3. The gel is then

4. The membrane is placed

5. The membrane is washed

6. The labeled probe is

 Now the expression

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