User:Catherine Koenigsknecht/Notebook/Experimental Biological Chemistry/2011/12/07: Difference between revisions

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==Notes==
==Notes==
This area is for any observations or conclusions that you would like to note.
NOTE: All procedure and results taken from lab partner Tamra, http://openwetware.org/wiki/User:Tamra_L._Fisher/Notebook/Experimental_Biological_Chem/2011/12/07
 


Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.
Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.

Revision as of 10:07, 26 December 2011

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Entry title

Objective

To see if the formation of purple protein fibers can be prevented when removing from heat if a refolding buffer is added first. Also, to see if the solution with fibers from yesterday also has purple solution.

Description

Studying the Effect of Refolding Buffer

  1. Mix 100μL of 2.9mM HAuCl4 and 100μL 17.7μM BSA with 800μL distilled water in a microcentrifuge tube.
  2. Place the tube on a heat block at 80°C for three hours.
  3. Add 500μL 50mM Tris, pH 7.5.
  4. Remove from heat after about 5 min. Observe and take a spectra.

Studying the Fibers and Solutions from Yesterday

  1. Centrifuge the microcentrifuge tube with purple protein fibers from yesterday (ratio=163.842) for 5 min at 13200rpm.
  2. Take a spectrum of the solution (without disturbing the pellet).
  3. Take spectra of other solutions from yesterday.

Data

Studying the Effect of Refolding Buffer

Picture of the microcentrifuge tube with the Au/BSA solution and refolding buffer. No fibers formed when the tube was removed from heat.


A spectrum was taken of this solution, which showed a peak at 534nm:

Studying the Fibers and Solutions from Yesterday

Spectra were taken of different solutions from yesterday:


A zoomed-in spectra shows a shift in peak. The solution that had fibers in it (highest ratio) has a peak around 544nm, and the next highest ratio has a peak shifted to about 533nm. From there the peak barely shifts. The solution with the lowest ratio did not show any purple or pink peaks:


Tube Number Ratio [Au]/[BSA] Wavelength Peak
1 163.842 544nm
2 131.073 533nm
5 65.5367 535nm
6 32.7684 N/A

Notes

NOTE: All procedure and results taken from lab partner Tamra, http://openwetware.org/wiki/User:Tamra_L._Fisher/Notebook/Experimental_Biological_Chem/2011/12/07

Use categories like tags. Change the "Course" category to the one corresponding to your course. The "Miscellaneous" tag can be used for particular experiments, as instructed by your professor. Please be sure to change or delete this tag as required so that the categories remain well organized.