Transformation of BL21 cells
The following procedures were conducted near the proximity of the Bunsen burner in accordance with aseptic techniques. The procedure is based from the laboratory Transformation protocol.
- Transferred 5 μL of PCR plasmid in two sterilized tubes. One tube will be filled with LB media, the other with SOC media. Both media are from Novagen.
- Added 40 μL of thawed BL21 cells into each tube. The tubes were immediately placed on a VWR analog heatblock at 42°C for 30 sec.
- After the 30 sec. mark, the tubes were submerged in ice. This rapid change in temperatures is a method of heat shock. This is an adequate of method of allowing the cells to incorporate the mutated plasmid into their intracellular matrix.
- Delivered 250 μL of the LB and SOC media using an automatic delivery pipet into the labeled tubes.
- The tubes containing the media were centrifuge for 1 h. at 37°C by Dr. Miller.
- During the latter of the lab period, 2 plates were inoculated for each cell grown in LB and SOC media.
- The first plate was inoculated with 50 μL of the BL21 cell grown in LB; the second plate was inoculate with a greater volume of cells with 200 μL.
- Dhea Patel plated the BL21 cells grown in SOC media.
UV-Vis of Au/lysozyme solution
- During the previous lab period of 10/23/12, the Au/lysozyme solutions were incubated at 50°C. The solutions were observed to this date to exhibit no fibers.
- Mole ratio 100 exhibited a slight purple tint. A UV-Vis scan was taken for this mole ratio. The graph of values are embedded below.
- The low temperature might have not denatured the lysozyme. Therefore, lysozyme could have not efficiently reduced Au (III) ito Au (0). The solution was re-incubated at a higher temperature, 85°C for 4h.
- As advised by Dr. Miller, the solutions were checked during the incubation period. There were observable aggregation as seen below. The photo below is for the mole ratio 170.
UV-Vis scans of Au/BSA