BME103:T930 Group 2 l2

BME 103 Fall 2012	Home People Lab Write-Up 1 Lab Write-Up 2 Lab Write-Up 3 Course Logistics For Instructors Photos Wiki Editing Help
OUR TEAM Error creating thumbnail: Unable to save thumbnail to destination Ryan Sullivan Research Development Scientist Error creating thumbnail: Unable to save thumbnail to destination Miriam Y Acosta PCR Machine Engineer Error creating thumbnail: Unable to save thumbnail to destination Ryan Keeney PCR Machine Engineer Error creating thumbnail: Unable to save thumbnail to destination Juliana Ramos Experimental Protocol Planner Error creating thumbnail: Unable to save thumbnail to destination Aaron Cornejo Experimental Protocol Planner LAB 2 WRITE-UP Thermal Cycler Engineering Error creating thumbnail: Unable to save thumbnail to destination Our re-design is based upon the Open PCR system originally designed by Josh Perfetto and Tito Jankowski. System Design Our new and improved PCR Machine encompasses a redesign where we improved the inner materials of the machine. By doing so, we can decrease the time it takes to duplicate the DNA samples, thanks to the new material, which is more insulating and responds more quickly to heat changes. Now, the PCR can be more effective and produce more samples in a given span of time. The modified PCR will also feature a larger capacity tube block. This will also make better efficiency and use of time. With the new tube block more tubes samples will be duplicated during a single run of the PCR. Finally, better quality wires and wire harness will be implemented in the new design. This is to facilitate the assembly and disassembly of the PCR, due to the previous version having very tight and hard to work with wiring. Key Features In addition, we made a change in the top lid of the Open PCR. We made one of the sides transparent to facilitate the tightening of the samples when they are placed in the rack. This way, one can easily see through the transparent side to check when the plate is secured on top of the sample lids. This will eliminate the possibility of over tightening which can damage the tubes and samples. Also, the new design will feature a side panel that is on a hinge. This is to make easier the access to the internal parts of the machine. The previous version had screws connecting the panels that were near impossible to work with. Finally, The other side panel will have a clip similar to that of a vaccum cleaner in which one can wind a long cord around. This makes is possible to have a longer power cord on the PCR machine. Instructions The instructions for use of the updated PCR are similar to the first. The larger tube block requires no further instructions. Also, the transparent side of the lid doesn't change any of the istructions, but rather makes the step of tightening the lid screw more simple. Similarly, having the higher quality wire harness makes no changes, but makes any instructions on disassemby and assembly much more simple. Finally the cord clip has the simnple instructions of winding a cord. Again, the addition of the hinged side panel does not add any new special instructions. Error creating thumbnail: Unable to save thumbnail to destination The main focus of the PCR is to be simple to use and have an easy, user-friendly interface. Our goal was to not to over complicate the system, but rather improve it. For that reason we have kept such instructions as the software interface and cycling the same. Protocols Materials Supplied in the Kit Amount Open PCR Machine 1 10 μM Forward Primer 16.0 μL 10 μM Reverse Primer 16.0 μL GoTaq Master Mix 800.0 μL dH2O 764.8 μL Eppendorf Tubes 16 Fluorimeter 1 Teflon Glass Slides 16 Allen Wrench 1 Operations Manual 1 Supplied by User Amount Screwdriver 1 Template DNA (20ng) 3.2 μL Micro-Pipetter 16 Camera Phone 1 PCR Protocol 1. Gather materials and assemble as shown in apparatus/manual 2. Label provided tubes with a number to indicate its sample. 4. With the micropipette, place the forward/reverse primer into the indicated tube. 5. Use a clean micropipette to place the master mix into the DNA/primer mixture in the tubes. 6. Transfer the 16 Eppendorf tubes containing DNA and Mix into the Open PCR Machine. 7. Open PCR program and input the number of cycles: 30. 8. Set the temperature and times into the program. - Denaturing temperature to 95°C. Time to 30 seconds. -Annealing temperature to 57°C. Time to 30 seconds. -Extending temperature to 72°C. Time to 30 seconds. 9. Close lid to commence process. 10. Start program. 11. When PCR is complete, ensue to the DNA Measurement Protocol shown below. DNA Measurement Protocol 1. Create 8 DNA template samples that will be the focus of the investigation and place them in the PCR Machine allowing them to complete the process and replicate. 2. Transfer each sample independently into its designated Eppendorf Tube with the 400mL buffer completely. Ensure that a single pipette is used per sample. 3. After setting up the fluorimeter, place 2 drops of SYBR Green onto the teflon slide followed by 2 drops of the sample you wish to use. (Again use the same pipette used to transfer the sample) 4. Align up the drop so the light is passing through it. 5. Take pictures of the drop using a camera or smartphone, these will later be uploaded to ImageJ for analysis. 6. Each slide is capable of handling 5 individual samples so simply place the drops in an empty space and repeat the process. 7. Also run drops from the scintillation vial as blanks using the same process. 8. Upload the pictures taken into Image J. 9. To analyze the images subtract the INTDEN measurement form the background from the INTDEN measurement form the drop and repeat for all trials. Research and Development Background on Disease Markers Sample A Sickle Cell Anemia rs35685286 [Homo sapiens] GGATGAAGTTGGTGGT--GAGGCCCTGG[A/G]CAGGTTGGTA--TCAAGGTTACAAGAC Chromosome 11- single nucleotide variation http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=35685286 Sample B Sickle Cell Anemia rs34430836 [Homo sapiens] AGGTGCTAGGTGCCTT--TAGTGATGGC[C/G]TGGCTCACCT--GGACAACCTCAAGGG Chromosome 11- single nucleotide variation http://www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi?rs=34430836 Disease Description Sickle cell anemia is an inherited blood disorder characterized primarily by chronic anemia and periodic episodes of pain. The underlying problem involves hemoglobin, a component of red blood cells. Hemoglobin molecules in each red blood cell carry oxygen from the lungs to body organs and tissues and bring carbon dioxide back to the lungs. In sickle cell anemia, the hemoglobin is defective. After hemoglobin molecules give up their oxygen, some may cluster together and form long, rod-like structures. These structures cause red blood cells to become stiff and assume a sickle shape. Unlike normal red cells, which are usually smooth and donut-shaped, sickled red cells cannot squeeze through small blood vessels. Instead, they stack up and cause blockages that deprive organs and tissues of oxygen-carrying blood. This process produces periodic episodes of pain and ultimately can damage tissues and vital organs and lead to other serious medical problems. Normal red blood cells live about 120 days in the bloodstream, but sickled red cells die after about 10 to 20 days. Because they cannot be replaced fast enough, the blood is chronically short of red blood cells, a condition called anemia. Inheritance Sickle cell anemia is an autosomal recessive genetic disorder caused by a defect in the HBB gene, which codes for hemoglobin. The presence of two defective genes (SS) is needed for sickle cell anemia. If each parent carries one sickle hemoglobin gene (S) and one normal gene (A), each child has a 25% chance of inheriting two defective genes and having sickle cell anemia; a 25% chance of inheriting two normal genes and not having the disease; and a 50% chance of being an unaffected carrier like the parents. Source: http://www.ornl.gov/sci/techresources/Human_Genome/posters/chromosome/sca.shtml Primer Design Sample A rs35685286 [Homo sapiens] Primer--CTCCGGGACCTGTCCAACCAT Reverse Primer-- GAGGCCCTGGACAGGTTGGTA Sample B rs34430836 [Homo sapiens] Primer--ATCACTACCGGACCGAGTGGA Reverse Primer--TAGTGATGGCCTGGCTCACCT Illustration Sample A This image illustrates the primer attaching to the reverse primer. The primer that is created attaches to the section of DNA that is mutated and is then able to be replicated with PCR, because it will allow the Taq polymerase to begin attaching nucleotides. Error creating thumbnail: Unable to save thumbnail to destination Sample B This image illustrates the primer attaching to the reverse primer. The primer that is created attaches to the section of DNA that is mutated and is then able to be replicated with PCR, because it will allow the Taq polymerase to begin attaching nucleotides. Error creating thumbnail: Unable to save thumbnail to destination Bayesian Information Sample A Affected Gene: HBB hemoglobin, beta Population Diversity: About 250 million people, and about 300,000 infants are born with a major hemoglobinopathies every year Probability of having mutation: 4.5%- of the world population [Source: Angastiniotis M, Modell B, Englezos P, Boulyzhenkov V. Prevention and control of hemoglobinopathies. Bull World Health Organ. 1995; 73: 375-386. - See more at: http://www.ispub.com/journal/the-internet-journal-of-biological-anthropology/volume-1-number-2/epidemiology-population-health-genetics-and-phenotypic-diversity-of-sickle-cell-disease-in-india.html#e-44] Sample B Affected Gene: HBD hemoglobin, delta Population Diversity: About 250 million people, and about 300,000 infants are born with a major hemoglobinopathies every year Probability of having mutation: 4.5%- of the world population [Source: Angastiniotis M, Modell B, Englezos P, Boulyzhenkov V. Prevention and control of hemoglobinopathies. Bull World Health Organ. 1995; 73: 375-386. - See more at: http://www.ispub.com/journal/the-internet-journal-of-biological-anthropology/volume-1-number-2/epidemiology-population-health-genetics-and-phenotypic-diversity-of-sickle-cell-disease-in-india.html#e-44]