Character Between Sonny's Blues vs a Rose for Emily Essay

At five minute intervals over the next fifteen minute period, record the color intensity of the solution of each test tube.

6. Repeat with each brand of towel and record the data. Repeat each set of trials at least four times for consistency of data.

Complete the experiment and save the PDF lab report. Do not answer the questions in the PDF lab report. Use the data in the PDF lab report

BEFORE CONDUCTING THE EXPERIMENT - You should already have submitted to your teacher an EXCELLENT Investigation Design that included:

Finally, place the 96 well plates in a CO2 incubator (37ºC) for 24 hours and read on a florescent

5.Wait 5 minutes. During these 5 minutes, set all 4 of the syringe plungers on the gas measuring mechanism at 2mL.

Then, measure the absorbance at the time that was decided as the optimal in step four.

 2.  Douglas has asked to take a sample of 10 sheets of rubber each hour from the extruder and measure the thickness of each sheet.  Based on the average thickness of the sample, operators will decide whether the extrusion process

Remove foam plug from the inoculate flask and pour it into a cuvette. Incubate it at 37°C and the optical density readings at 600nm every 10-15 mins. Pour into the

Use a stopwatch to time 5 cycles and record the time in the data table.

eliminate water within the mixture and to form the desired paper thickness. The material then proceeds to a drying

Empty and clean the test tubes and repeat steps 2-10 again for a second dataset.

The first experiment was Baseline and for that experiment we needed to get three tubes but one of the tubes were already done so the only thing was left is to do test tube two and three and put it together than put it in the spectrophotometer 20. The hypothesis for this experiment

Following that, a blotting sandwich is made by adding blotting buffer to the container and inserting the plastic cassette. Lay a wet fiber pad on the black side of the cassette. On top of that lay a wet blotting paper on the fiber pad and then roll a pen lightly across to get the air bubbles out. Place the gel on top of the previous layer and then lay a wet nitrocellulose membrane on the gel. Another wet blotting paper and fiber pad are placed on top of the gel. Once this is complete, close the cassette and set up the Mini Trans-Blot module. Fill with blotting buffer up to the top and then blot for 2.5 hours at 20V.

7.When water bath is ready, put each test tube into the water bath. Wait 5 minutes.