User:Puja Mody/Notebook/Chem 571: Gold Nanoparticles/2012/11/07

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Bradford Assay

Goals

Procedure

  • A stock solution of 1mg/mL BSA was prepared by adding 10mg of BSA into a 10mL volumetric flask and then filling it with autoclaved water. The actual concentration of the BSA stock was 1.02mg/mL as the actual weighed out BSA added was 10.2mg BSA.
  • In order to determine the concentration of the ADA collected in the fracs, standard solutions had to be made and run through the UV-Vis first. Seven standard solutions were prepared with 1X Bradford Reagent, varying amounts of BSA stock, and autoclaved water. These solutions were analyzed in the UV-Vis from 500-800 nm.
Volume 1X Bradford Reagent Added [mL] Volume BSA Stock Added [mL] Volume Water Added [mL] Conc. BSA [mg/mL]
1.400.030
1.40.0050.0250.003566434
1.40.010.020.007132867
1.40.0150.0150.010699301
1.40.020.010.014265734
1.40.0250.0050.017832168
1.40.0300.021398601


  • The absorbance values at 595 nm of each solution were graphed versus BSA concentration in mg/mL to produce a calibration curve.
  • Using linear regression, the equation of the line was obtained.

Image:Bradford_assay.png

  • Fractions of ADA, made on 2012/10/03 and 2012/11/06, were obtained.
  • 7.5 μL of each fraction was added to 7.5 μL of autoclaved water and 715 μL of 1X Bradford reagent.
    • Fraction #2, obtained in November, was diluted by half, using the same procedure as listed above for the standard solutions, such that its absorbance was below 1.
Sample Name Volume of ADA [mL] Absorbance [] Conc. ADA [mg/mL] Mass of ADA [mg] Moles of ADA [mol] Molar Absorptivity of ADA [mL/mg cm] Molarity [M]
  • When these samples were originally run, they produced absorbances over 1 which resulted in us needing to dilute the solution further. As a result, all solutions were diluted by a half to 715μL of original solution with an additional 715μL of water.


DATA


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