blotting and their types

1. Blotting techniques
AYYA NADAR JANAKI AMMAL COLLEGE
Department of Microbiology
M.Veeralakshmi
18PY21
II Msc, Microbiology

2. What is blotting
 Blotting is the technique in which nucleic acids or proteins are
immobilized onto a solid support generally nylon or
nitrocellulose membranes.
 Blots are techniques for transferring DNA , RNA and proteins
onto a carrier so they can be separated.
 The method is involves separation,transfer and hybridization.
.

3.  . The southern blot is used to detect the presence of a
particular piece of DNA in sample. Southern blot named after
Sir Edwin Southern Developed in 1975 .
 The DNA detected can be a single gene, or it can be part of a
larger piece of DNA such as a viral genome.
 This technique is hybridization or blotting.

6. Pri nciple
• Hybridization: It is the process of forming a
doublestranded DNA molecule between a single-
stranded DNA probe and a single-stranded target
DNA.
• There are 2 important features of hybridization:
• The reactions are specific-the probes will only
bind to targets with a complementary sequence.
• The probe can find one molecule of target in a
mixture of millions of related but non-complementary
molecules.

7. Overall steps of blotting
• .DNA Fragmentation
• Agarose Gel Electrophoresis
• Depurination (optional)
• Neutralization
• Blotting
• Prehybridization and Hybridization
• Removal of Unbound Probe
• Autoradiograph

8. materials
• Solutions:
1) 0.25N HCl Stock HCl is 12N 20.8ml of HCl 979.2ml of
ddH2O = 1 Liter
2) Solution D Denature solution 1.5M NaCl 87.75g 0.5M
NaOH 20.00g ddH20 to 1 Liter
3) Solution N Neutralizing solution 0.5M Tris 60.50g, 1.5M
NaCl 87.75g , 1mM EDTA 0.372g ddH2O to 1 Liter pH to
7.5
4) 20 X SSC 3.0M NaCl 175.30g 0.3M NaCitrate 88.2g
ddH20 to 1 Liter ,pH to 7.0.

10. DNAfragmentation
• DNA is digested by one or several restriction
enzymes ( bacterial enzymes )
• cut at specific sequence (restriction site)

11. Agrogel electrophoresis
• Restriction fragments are separated electrophoretically
by size on agarose gel.
• • DNA fragments migrate into gel toward the anode
(+ve electrode) under the influence of electric field
because it is negatively charged

12. De-purination
• When DNA fragments is > 15 kilobases, it is too hard
to be transferred to filter.
• The gel is treated with dilute acid (0.2 M HCl for 15
minutes) to have smaller pieces can trans.

13. Neutralization:
• DNA is placed into an alkaline solution containing
0.5mM NaOH to denature the dsDNA into ssDNA
and neutralize the acid in previous step.
• Function of Neutralization :
(1) improve binding of the –ve charged DNA to
+ve charged filter
(2) ssDNA strands for hybridization
(3) destroy any remaining RNA present in the
sample

14. Neutralization

15. Blotting
• Setps:
I-Cover gel with nitrocellulose paper.
II-Cover nitrocellulose paper with thick layer of
paper towels.
III-Compress apparatus with heavy weight.
IV-ssDNA binds to nitrocellulose at same position it
had on the gel.
• V-Vacum dry nitrocellulose at 80 C to permanently
fix DNA in place or cross link (via covalent bonds) the
DNA to the membrane.

16. Setup of blotting

17. Hybridization
• Incubate nitrocellulose sheet with a minimal quantity
of solution containing 32P-labeled ssDNA probe.
• Probe sequence is complementary to the DNA of
interest.

18. Removal of Unbound Probe
• Unbound probe is washed off.

20. Autoradiograph
• is an image on an x-ray film
•The location of the probe is revealed by converting a
colorless substrate to a colored product that can be seen
orgives off light which will expose X-ray film.
•The bands indicate the number and size of the DNA
fragments complementary to the probe.

22. Application of southern blotting
• Identify specific DNA sequences in DNA samples
• Isolate desired DNA for construction of rDNA.
• Identify mutations, deletions and gene rearrangements.
• In GMOs, used for testing to ensure that a particular section of DNA
of known genetic sequence has been successfully incorporated into
thegenome of the host organism.
• Phylogenetic analysis
• To determine the number of copies of a particular DNA sequence
• In DNA Fingerprinting for:
– Paternity & Maternity tests
– Forensics
– Personal/ Bio identification

23. Diagnosis of human disease
• Detect point mutation, gene rearrangement or gene
amplification
–Mutated gene change in the size (hemophilia A)
–Gene rearrangement change in size and pattern (leukemia)
–Amplification increase in gene copy number (Charcot-Marie-
Tooth syndrome

24. Main functions
• Detect the specific DNA sequence (gene) of
interest.
• Determine the length of the restriction
fragment carrying the sequence.
• Detect the restriction site.

25. Disadvantages of southern blotting
• More expensive than most other tests.
• Complex and labor-intensive.
• Time consuming an combersome.
• Requires a large amount of targeted DNA.

27. Intro of northern blotting
• The northern blot is a technique used in molecular
biology to study gene expression by detection of
RNA (or isolated mRNA) in a sample.
• Developed by Alwnie and his colleagues in 1979.
• This method was named for its similarity to the
technique known as a Southern blot.

28. Steps of northern blotting
• No need to digest RNA with restriction enzymes.
• Extraction of RNA:
The RNA sample can be:
i. total RNA isolated from particular samples
• ii. RNA containing poly(A) tails, i.e: messenger
RNA(mRNA)

29. Cont….
• Extraction of total RNA from a homogenized
tissue sample or from cells.
• mRNA isolated through the use of oligo (dT)
cellulose chromatography to isolate only those
RNAs with a poly(A) tail.

30. Gel electrophoresis
• RNA samples are then separated by gel electrophoresis.
• In gel electrophoresis the mixture of mRNA molecules
separated/denatured to small fragments/molecules according to
their size using an electric field.
• Formaldehyde :
Formaldehyde is used to unfragment the branched RNA
molecule to simple linear one and to prevent it form coiling
again.

32. Blotting
• The transfer or blotting is the step in which the mRNA from
the electrophoresis gel will be transferred onto a nylon
membrane.
• Traditionally, a nitrocellulose membrane is used, although
nylon or a positively charged nylon membrane may be used.
• Nitrocellulose typically has a binding capacity of about
100μg/cm, while nylon has a binding capacity of about 500
μg/cm. Many scientists feel nylon is better since it binds more
and is less fragile.
• RNA,s will be covalently link to membrane.

33. Blotting setup for northern

34. Hybridization
• In molecular biology hybridization means the process
of forming a double stranded nucleic acid from joining
two complementary strands of DNA (or RNA).
• Incubate membrane with labeled DNA or RNA probe
with target sequence

36. Washing And Visualization
• Wash Nylon from excess of probe & dry.
• Place Nylon sheet over x-ray film.
• X-ray film darkens where the fragments are
complementary to the radioactive probes.

37. Advantages/Application
• Observe a particular gene's expression pattern
between tissues, organs, developmental stages,
environmental stress levels, pathogen infection, and
over the course of treatment.
• Used to show overexpression of oncogenes and down
regulation of tumorsuppressor genes in cancerous
cells.
• Detecting a specific mRNA in sample, used for
screening recombinants which are successfully
transformed with transgene.
• mRNA splicing studies

39. Main functions
• Detect mRNA transcriptional activity
• Quantifying the transcription
• Determine the size of the mRNA
• Determine mRNA level

41. • Western blotting is a widely used analytical
technique in molecular biology to detect
specific protein in a sample of tissue
homogenate or extract.
• It works on the principle of gel
electrophoresis.
• Proteins are separated based on their size on
polyacrylamide gel

42. Cont….
• The method originated in the laboratory of
Harry Towbin at the Friedrich Miescher
Institute, Switzerland in 1979.
• The name western blot was given to the
technique by W. Neal Burnette and is a play on
the name Southern blot.

44. Sample Preparation

45. Gel Electrophoresis
• Electrophoresis is commonly used method for
separating proteins on the basis of size, shape or
charge.
• In Gel electrophoresis, protein of sample extract are
separated according to their molecular weight.
I-Samples are loaded into separate wells
II-Run at 200 volts for 30-40 minutes
III-Running Buffer (pH 8.3)

48. Protein transfer
• On completion of the separation of proteins
by polyacrylamide gel electrophoresis, the
next step is to transfer the proteins from the
gels to solid support membrane.

49. Protein staining
• After gel electrophoresis, it may be necessary to
confirm that all the proteins in the gel have been
completely eluted.
• Proteins are usually stained with dyes such as
coomassie blue, silver stain, or deep purple.

51. Blocking
• For meaningful results, the antibodies must bind
only to the protein of interest and not to the
membrane.
• Non-specific binding (NSB) of antibodies can be
reduced by blocking the unoccupied sites of
membrane with an inert protein or non-ionic
detergent.
• Blocking agents should possess greater affinity
towards membrane than the antibodies.

52. Blocking agents
• The most common blocking agents are:
a) Bovine serum albumin(BSA)
b) Non-fat milk
c) Casein
d) Gelatin
e) Dilute solution of Tween 20

53. Labeling with Primary Antibody
• forms an antibody-protein complex with the
protein of interest with specific Antibody.
• Labeling with Secondary Antibody:
Is conjugated to HRP (horseradish
peroxidase)
Acts as antibody against primary antibody
Antigens can be visualized through
colored reaction

55. washing
• Unbound antibodies can cause high
background and poor detection.
• Hence Washing the blot removes unbound
antibodies from the membrane.
• A dilute solution of tween-20 in TBS or PBS
buffer is commonly used for washing

56. Protein detection
• After the unbound probes are washed away,
the western blotting is now ready for
detection of the probes that are labeled and
bound to the protein of interest.
• Enzymes such as alkaline phosphatase(AP), &
Horse-radish peroxidase(HRP) are widely used
in detection of proteins

59. Analysis and imaging
• This is the last & major step of the western blotting
technique.
• Detection of signals, using either X-Ray film, scanners
or a CCD, results in one or more visible protein bands
on the membrane image.

61. application
• Analysis Of IgG Fractions purified from human plasma.
• Diagnosis of HIV by ELISA, involves the western blotting
technique.
• Western blotting technique is also used to Detect Some Forms
Of Lyme Disease.
• Western blotting technique is used in Definitive Test For BSE,
which is commonly know as Mad cow disease.
• Confirmatory Test For Hepatitis-B involves western blotting
technique.
• Western blotting test is used in the Analysis Of Biomarkers
such as hormones, growth factors & cytokines.
• This technique is also employed in The Gene Expression
Studies.