From the gel electrophoresis, we found that the PCR product was about 600 bps. Spectrometric analysis helped us to find the concentration of amplified DNA which was about 65 μL/mL. The next step was to produce digoxigenin-UTP labelled RNA probe by in vitro transcription of PCR amplified tau DNA with T7 RNA polymerase. About 4 μL of template DNA was added to a sterile, RNase-free reaction vial. The total sample volume was made up to 13 μL by adding water.
Then 5mL of HCl was added to copper to completely remove all traces of zinc. Once the bubbling had stopped, the rest of the liquid was decanted away from the copper. Then the copper recovery set up was put together using tubing, Buchner funnel, filter paper and suction flask. Then the filter paper was weighed before placing it in the funnel and wetted down. The aspirator was turned to medium high, and then the copper was poured onto wetted filter paper.
The purpose of this lab is to focus on how to make zinc iodide in a different way using compounds instead of elements, which are barium iodide and zinc sulfate. We will see if the reaction between these two compounds will occur and make a prediction by writing a chemical equation. The procedures for this lab are to place a small test tube inside a 50mL beaker and weigh it. Then, using a spatula, add 0.45±0.03 g of zinc sulfate heptahydrate into the small test tube and record the mass. After that, dissolve the sample in 2 mL of deionized water and shake the test tube for 1 to 1 ½ minutes to dissolve the solid.
Burst the cellular membrane and the nuclei What is the name of the process used to amplify DNA? Polymarse Chain Reaction How is the amplified DNA sorted? By size What # did the DNA profile match? #3 Why was Greg’s DNA profile in CODIS? Because all forensic scientists are required to have their DNA in CODIS Toxicology Lab: Where is vitreous humor normally located?
5mL of acidified water will be measured, using a graduated cylinder, and will be transferred to the R tube, and will be immediately vigrously mixed with the reactants. Once the solution turns to an orange or red-brown color, a pipet will be used to quickly remove 30 drops of the solution, then transferred to the C tube, and the mixing will resume until the solution is close to room temperature. The solution will be filtered into the P tube, and the solution that is left in the R tube should be washed three times with 1mL of acidified water each time. The water should then be poured into the P tube, leaving the solid in the R tube. Using a test tube holder, heat the R tube over the Bunsen burner, moving the tube in a circular motion until all the water has evaporated.
We now slowly pour the solution into a funnel with filter paper. The extract along with 2 pieces of Iodine are added to a new beaker and left for 10 minutes. Finally to determine if the lab was successful, three tests are conducted for Iodine, Iodide and triiodide. The objective is to produce a tincture of iodine by extracting iodide and other components from seaweed. Warm up Activity 1.
-Use the titrations of the following chemical reactions: NaHCO3 + HCl (aq) NaCl (aq) + H2O (l) + CO2 (g) 2HCl (aq) + Na2CO3 (s) 2NaCl (aq) + H2O (l) + CO2 (g) Experimental procedure- Two Erlenmeyer flask must be labeled “unknown 1 and unknown 2”. Assure that all containers used are dried and cleaned properly. Two bigger flask are labeled “waste” according to each unknown. A pipette is set up and primed with HCl. The two unknown solids are weighed to a mass of 0.15g each.
The liquid of homogenate was filtered into a beaker through Miracloth (2 layers cloth) to remove large plant components and 1 ml of the filtrate was transferred to a conical tube. 8.4 g of ammonium sulfate was slowly added to the 40 ml of the filtrate as it was stirred on a stir plate for 15 min to achieve 37% saturation (210g/L of solution). The solution was then centrifuged at a speed of 9000 x g at 4oC for 15 min to sediment the proteins. The resultant supernatant 1 was transferred to a beaker with 1 ml transferred to a conical tube and the obtained pellet 1 was resuspended in 4 ml of distilled water and transferred into a dialysis bag to remove the salt. Then, 3.4 g of ammonium sulfate was slowly added to the supernatant 1 as it was stirred for 15 min to achieve 50% saturation (85g/L of solution).
It's time justice put the emphasis of our criminal justice system back on protecting the victim rather than the accused. Any criminal on death row has almost always committed another crime to add onto their punishment. DNA testing and other methods of modern crime scene science can now effectively eliminate most uncertainty as to a person's guilt or innocence. Death penalty pros states that “DNA testing is over 99 percent effective. And even if DNA testing and other such scientific methods didn't exist, the trial and appeals process is so thorough it's next to impossible to convict an innocent person”.
You may spool the DNA on your glass rod or pipette tip. 10. Spool the DNA by dipping a pipette tip or glass right where the extract layer and alcohol are in contact with each other. With your tube at eye level, twirl the rod and watch as DNA strands collect. Data: | Amount Added or Obtained | Initial Color | Purpose | Buffer | 10 ml | blue | Break through the cell membrane | Strawberry | 1 | red | Subject tested