The polymerase chain reaction is a laboratory process in which a specific sequence of deoxyribonucleic acid (DNA) is amplified producing many copies of the specific DNA sequence. However, their must be components such as (DNA template, primers, DNA polymerase, deoxyribonucleotide triphosphates (dNTP’s), buffer solution, and magnesium chloride salt solution) are required to carry out the process which undergoes through three major stages to make the copies of DNA segment. First stage is denaturation, after that annealing, then extension. However, this can be done if and only if the 3’ and 5’ ends are known, this helps in initiating DNA synthesis in which it is ensured that two short oligonucleotides acts as primer will anneal onto DNA strands. Polymerase chain reaction process is used as a diagnostic and research tool due to the fact that it can be done within a few hours which makes it a rapid assay.
The polymerase chain reaction is made in an automated machine called thermocycler which can increase and decrease the temperature quickly. The components are mixed together in a tiny volume tube. In
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The process can be used for early diagnosis such as test for genetic disease, infectious disease, and cancer. Furthermore, the quantitative polymerase chain reaction use molecular finding to identify the disease instead of the physiological symptoms. It can detect the AIDS virus within the first few weeks after infection. Also it can identify the number of specific sequence of DNA present in a sample. This can help in diagnostic of disease as well as in the researches. Both the quantitative and qualitative polymerase chain reaction can distinguish the genes involved in the development of cancer, which can helps in the treatment due to the fact that these genes are able to determine the progression of the disease and an impact in the effectiveness of the
The STR length contrast is what is used to differentiate individuals. Gel electrophoresis then uses the STRs to create a DNA profile. The gel electrophoresis separates the STRs depending on their length and the pattern is then shown in fluorescent gel creating the profile. These profiles are then used by scientist to compare patterns between evidence and or suspects to determine a match or not a match.
The Solid sequencing platform, produced by Technologies/Applied Biosystems (ABI), performs sequencing by ligation method. Similar like the Roche 454 library preparation, genomic double strand DNA were sheared into small pieces and ligated with two types of adatptors P1 and P2 on two ends. One end with P1 adaptor binds onto the surface of the magnetic bead and emulsion PCR takes place to amplify single nucleotide fragment. Then the oil was washed out and four fluorescent labeled di-bases probes were added into the beads mixture. By matching the 1st and 2nd position of the template by di-base probes, fluorescence was detected and the extra tail with fluorescent probe is cleaved out.
A laser hits the fluorescent colors to deliver light which is recognized by a confocal scanner. The scanner then creates a computerized picture from the energized microarray. The advanced picture is further handled by particular programming to change the picture of every spot to a numerical reading. The way toward measuring quality expression by means of cDNA is called expression analysis or expression profiling. By finding which genes in cancer cells are mutated, scientists can better analyze and treat growth.
Group 2 Hela Essay Henrietta Lacks was a normal, young African American woman who lived a simple life by taking care of her family, including her husband (and also her first cousin) Dale, and their five children. Not long after she delivered her fifth child, Henrietta developed an aggressive cervical cancer caused by the sexually transmitted disease, HPV, which quickly caused her to lose her fight and pass away, yet her death and cancer cells also had a new beginning in the aspect of science: her cells taken from a biopsy continued to divide and became one of the most important cell lines in medical history.
DNA Fingerprinting Using Agarose Gel S. Aaron Sowards Bio 122 Lab 04 Brianna Adanitsch Jakob Lester Minhenga Ngijoi 2/21/18 Dr. Chad R. Sethman Abstract DNA fingerprinting is the process of analyzing an individual’s DNA base-pair patterns. The DNA fingerprinting lab involved identifying the suspect using Agarose Gel and Polymerase Chain Reaction. It was found that suspect two s DNA matched the crime scene DNA.
It has become a powerful tool in the criminal justice system, it provides conclusive evidence that can link a suspect to a crime, help free individuals who have been wrongfully convicted of crimes, and identify victims of crimes who are deceased. DNA evidence is analyzed through a PCR (polymerase chain reaction) this method allows for the smallest specks of any type of DNA. (Staff) In the criminal justice system, there are many ways that DNA evidence is used in we use it to Identify suspects, DNA evidence collected from a crime scene is sent off and compared to DNA samples collected from suspects or from a DNA database. To determine if a suspect's DNA matches the DNA found at the crime scene.
What is the term for the random arrangement of homologous pairs of chromosomes during the first division of meiosis? Independent Assortment 5. What role does the Polymerase Chain Reaction (PCR) play in producing a DNA Profile? PCR amplifies the regions of DNA with short tandem repeats and uses primers with fluorescent labels. This works by replicating the region of DNA several times.
4. Molecular Diagnosis Parasite nucleic acids are identified by using the polymerase chain reaction (PCR). Even though this technique may be somewhat more susceptible than microscopy, it is of restricted effectiveness for the diagnosis of acutely ill patients in the standard healthcare setting. PCR results are often not obtainable rapidly enough to be of value in establishing the diagnosis of malaria infection. PCR is mostly beneficial for verifying the species of malarial parasite after the diagnosis has been recognized by either microscopy or RDT.
Introduction On October 19th 1992 witnesses believed they saw twenty three year old Laura Houghteling leave her Bethesda home, not knowing in fact that it was Hadden Clark, a part time gardner who worked for the Houghteling family. What would follow this sighting, and the subsequent missing persons report of Laura Houghteling would be a fascinating murder investigation which would lead to a precedent setting conviction and the capture of a serial killer. This report will investigate the method of Mitochondrial DNA analysis through the DNA typing method of RFLP or Restriction Fragment Length Polymorphism. The report will explore the mechanisms of the technique itself along with the benefits and limitations of the technique. This case is
The unknown #257 tested positive for the enzyme DNase. Lastly, Mannitol Salt Agar (MSA) was used to test for isolation and differentiation. The streaking technique used is streaking for isolation. The unknown #257 tested positive for mannitol fermentation which means the organism is
DNA in Forensic Science DNA is the carrier of genetic information in humans and other living organisms. It has become a very useful tool in forensic science since it was discovered. In forensic science, DNA testing is used to compare the genetic structure of two individuals to establish whether there is a genetic relationship between them. One example of the use of DNA in forensic science that is important in biology today is comparing a suspect’s DNA profile to DNA that was discovered at a crime scene.
The DNA gathered by the group bore positive results only on Test for Deoxyribose; compared to the standard solution, which bore positive results on all chemical tests, namely, Test for Deoxyribose, Test for Phosphate, Test for Purines, and test for Pyrimidines. Introduction Nucleic Acid is one of the essential biochemical molecules
Finally, the amplified DNA regions are compare using a gel. DNA Profiling
This can be tested by simply mixing the serum of suspected individual which contain the antibodies with the antigens of specific bacteria the accumulation of clumps confirms the presence of particular bacterial infection.[2] This test can be performed in various ways including slide agglutination reaction, tube agglutination reaction, indirect agglutination inhibition reactions etc. Another important practical application involves blood group test of