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INTERNATIONAL SCHOOL
NAME:AZMATH NAFISA
CLASS: XII
BIOLOGY INVESTIGATORY PROJECT
TOPIC: DNA FINGER PRINTING
CERTIFIC
ATE
This is to certify that Azmath Nafisa ,a student of
class XII has successfully completed the project
under the guidance of Miss Jyotimaryee Swain
during the academic year 2022-2023 in partial
fulfilment
of biology practical examination conducted by
CBSE.
INTERNAL EXTERNAL
EXAMINER EXAMINER
PRINCIPAL
ACKN
OWLE
In the accomplishment of this project successfully,
many people have best owned upon me their
DGEM
blessings and the heart pledged support, this time I
ENTto thank all the people who have been
am utilizing
concerned with the project.
Primarily I would like to thank God for being able
to complete this project with success. Then I
would like to thank my principal Dr. Swarupa
Nanda and biology teacher Miss Jyotirmayee
Swain, whose valuable guidance has been the ones
that helped me patch this project and make it full
proof success her suggestions and her instructions
has served as the major contributor towards the
completion of this project.
Azmath Nafisa
XII
CONTE
NT
Introduction
Principle of DNA fingerprinting
Applications of DNA fingerprinting
Advantages and disadvantages
Uses of DNA fingerprinting
Uses of DNA fingerprinting in Forensic
Science
Conclusion
Bibilography
INTRO
DUCTI
1980 – American researches discovered
non-coding regions of DNA.
ON
1984- Professor Alec Jeffreys developed
the process of DNA profiling.
1987- First conviction based on DNA
evidence.
"DNA fingerprinting is a procedure that shows
the hereditary cosmetics of living things. It is a
strategy for finding the distinction between the
satellite DNA areas in the genome.“
DNA profiling, DNA testing, DNA
examination, Genetic profile, DNA
distinguishing proof, genetic fingerprinting,
and genetic investigation are a portion of the
mainstream names utilized for DNA
fingerprinting. This technique was invented by
Alec Jeffreys in 1984.
PRINCIPL
E OF DNA
FINGERP
The human genome consists of innumerable small
noncoding sequences which are inheritable and
repeatedly present. They can be separated from the
bulk DNA as satellite upon performing density
gradient centrifugation and thus known as satellite
DNA. They can be categorized into either
microsatellites or microsatellites depending on the
length, base composition and tandemly repetitive
units. These satellite DNAs show polymorphism
and this polymorphism is the basis of DNA
fingerprinting. The repeat regions can be divided
into two groups based on the size of the repeat–
variable number tandem repeats (VNTRs) and
short tandem repeats. These repeats act as genetic
markers and every individual inherits these repeats
from their parents. Thus, every individual has a
particular composition of VNTRs and this is the
main principle of the DNA fingerprinting
technique.
DNA
FINGERof organic example blood, spit,
1.Collection
PRINTI
buccal swab, semen, or solid tissue.
NGextraction.
2.DNA
STEPS absorption or PCR intensification.
3.Restriction
4.Agarose gel electrophoresis slim
electrophoresis or DNA sequencing.
Interpreting outcomes
THE
PROCE
Sample collection, DNA extraction, absorption or
intensification and investigation resultsSS are OF
significant advances. DNA
Stage 1: Sample Collection
FINGE
DNA can be acquired from any bodily sample or
liquid. Buccal smear, salivation, blood,RPRIN
amniotic
liquid, chorionic villi, skin, hair, body liquid, and
TING
different tissues are significant kinds of samples
utilized.
Stage 2: DNA Extraction
We need to initially get DNA. To play out any
genetic applications, DNA extraction is one of the
most significant advances. Great quality and
amount Of DNA expands the conceivable
outcomes of getting better outcomes.
You can utilize DNA extraction strategies enrolled
beneath,
1.Phenol-chloroform DNA extraction strategy
2.CTAB DNA extraction strategy
3.Proteinase K DNA extraction strategy
In any case, we emphatically prescribe utilizing a
ready to go DNA extraction unit for DNA
fingerprinting.
The immaculateness and amount of DNA ought to
be ~1.80 and 100ng, individually to play out the
DNA test. Filter the DNA utilizing the DNA
sanitization unit, if necessary.
From that point onward, measure the DNA
utilizing the UV-Visible spectrophotometer.
Furthermore, perform one of the accompanying
strategies recorded underneath.
Stage 3: Restriction Absorption, Enhancement
or DNA Sequencing
Three regular strategies are utilized:
1.RFLP based STR investigation:
Everyone has genetic sequences called variables
number tandem repeats, or VNTRs –The VNTRs
make the different sized RFLPs.
2.PCR based investigation
If there is only a small amount of DNA
available for DNA Fingerprinting – augment
the amount of DNA using a technique called
PCR. PCR is doing DNA replication in a test
tube.
Like all DNA polymerases.
Taq polymerase can only add to the 3’ end
of an existing nucleotide.
A DNA primer that is complementary to
the template is used to supply that 3’ end.
Stage 4: Analysis of Results
As we examined, utilizing the southern blotting,
agarose gel electrophoresis, narrow
electrophoresis, ongoing intensification, and DNA
sequencing, the outcomes for different DNA
profiling can be gotten in which rt-PCR and
sequencing are much of the use in forensic
science.
Stage 5: Interpreting Results
By looking at DNA profiles of different examples,
varieties and likenesses between people can be
distinguished. Outstandingly, the whole procedure
is presently nearly automatic. We don't need to do
anything, the computer gives us conclusive
outcomes.
APPILIC
ATION
OF DNA
• Utilizing the DNA fingerprinting strategy, the
FINGERP
natural personality of an individual can be
RINTING
uncovered. For approving one's character,
there is no other preferable alternative over
DNA fingerprinting.
• Gravely harmed dead bodies can be
distinguished.
• It is utilized to detect maternal cell
contamination.
• One of the significant downsides of pre-birth
determination is maternal cell tainting. The
amniotic liquid or CVS test contains the
maternal DNA or maternal tissue, once in a
while. Contamination expands the opportunity
of false-positive outcomes, particularly
onaccount of carrier recognition. Utilizing
VNTRs and STRs markers with PCR-gel
electrophoresis, maternal cell tainting can be
recognized during pregnancy hereditary
testing.
• One of the most significant uses of the current
strategy is in the crime scene examination and
criminal check. The example is gathered from
the crime site which could be salivation,
blood, hair follicle, or semen. DNA is
removed and investigated against the suspect,
utilizing the two markers we clarified
previously. By coordinating DNA band
designs criminal's connected to wrongdoing
can be built up.
ADV
ANT
ADVANTAGES:
AGE
1.It is an easy and painless method for the subject
S It is less invasive then taking a blood
being tested.
AND
sample
DISA
2. It is an affordable and reliable technique
3. ItDVA
can be conducted in a relatively short amount
NTA
of time
4. Anyone at any age can be tested with this
GES
method without any major concerns
HY