User:Melissa Novy/Notebook/CHEM-571/2012/09/05

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(UV-Vis Analysis)
(Notes)
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==Notes==
==Notes==
* Please refer to [[User:Keyun_Wang/Notebook/Experimental_Biological_Chemistry_I/2012/09/05|Keyun Wang's entry]] for observations on making and centrifuging Au/BSA solutions.
* Please refer to [[User:Keyun_Wang/Notebook/Experimental_Biological_Chemistry_I/2012/09/05|Keyun Wang's entry]] for observations on making and centrifuging Au/BSA solutions.
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* Please refer to [[User:Dhea_Patel/Notebook/Experimental_Biological_Chemistry_Notebook/2012/09/05|Dhea Patel's entry]] for volumes and calculations used in remaking the Au/BSA solutions.
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Revision as of 14:12, 11 September 2012

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Objectives

  • Prepare serial dilutions of 0.1 M Tris buffer stock solution at the following concentrations: 10 mM, 1 mM, 100 μM, 10 μM.
  • Remake Au and BSA stock solutions to check for contamination.
  • Resuspend Au/BSA fibers in different concentrations of pH 8 or 10 Tris buffer.

Au/BSA Fibers

  • Protocol for Resuspending Au/BSA Fibers
    1. Au/BSA solutions were centrifuged at 3000 rpm, 25°C, for 5 min, such that the fibers formed a pellet at the bottom of the centrifuge tube.
    2. 1 mL of 10 mM pH 8 Tris buffer was added to each pellet and pipetted up and down to resuspend the fibers.
    3. Step two was repeated with Tris buffer at concentrations of 1 mM, 100 μM, and 10 μM on fibers with arbitrary Au/BSA mole ratios.
    4. Steps 2 and 3 were repeated with pH 10 Tris buffer.
  • UV-vis spectroscopy was conducted on the resuspended fiber solutions.

UV-Vis Analysis

Image:9-5-12_Absorbance_AuNP-BSA_Tris_Buffer.JPG

  • Absorbance of AuNP/BSA fibers resuspended in Tris buffer at concentrations of 100 μM, 10 μM, 1 mM, and 10 mM and pH of 8 or 10.

Notes

  • Please refer to Keyun Wang's entry for observations on making and centrifuging Au/BSA solutions.
  • Please refer to Dhea Patel's entry for volumes and calculations used in remaking the Au/BSA solutions.


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