Difference between revisions of "Lidstrom:BCA assay"

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*Our kit: Pierce BCA Protein Assay Kit (Prod #23225). [http://www.piercenet.com/instructions/2161296.pdf manual]
*Our kit: Pierce BCA Protein Assay Kit (Prod #23225). [http://www.piercenet.com/instructions/2161296.pdf manual]
*Use the microplate procedure
*Use the microplate procedure
*Use the buffer your samples are dissolved in for the diluent.

Revision as of 12:37, 27 May 2013


  • BCA is a general use kit to determine total protein concentration prior to Western blot or other protein analysis
  • Our kit: Pierce BCA Protein Assay Kit (Prod #23225). manual
  • Use the microplate procedure
  • Use the buffer your samples are dissolved in for the diluent.


  • BCA reagent A
  • BCA reagent B
  • 96 well plate
  • Microcentrifuge tubes
  • Microcentrifuge tube rack
  • Microcentrifuge
  • BSA stock (2 µg/ µl)
  • Pipette
  • Pipette tips


  1.  ?? Do you need to turn on the plate reader and warm up the lamp??
  2. Plan & Prepare your samples & dilutions
    1. Make three concentrations of each of in sets of three new microcentrifuge tubes labeled with their dilution or tube number. Full concentration, 2x dilution and 10x dilutions are usually sufficient.
    2. You will need 25 uL of each sample per well. Consider doing technical replicates.
  3. Prepare Standards ( 2 fold dilutions): 2 µg/ µl, 1 µg/ µl, 0.5 µg/ µl, 0.25 µg/ µl, 0.125 µg/ µl
    1. You need at least 1mL of the full-concentration sample (A) to do the dilutions below, so weigh at least 2ug in an eppendorf tube.
    2. Preparing BSA standards for BCA total protein assay
  4. Prepare BCA Working Reagent
    1. For the total volume of working reagent calculate:
      • (# standards (in our case 5) and samples (30 in our case))*(# replicates (2))*(volume of working solution per sample (200 µl))
    2. Prepare working reagent (WR) standards for Pierce kit
    3. To prepare working solution mix 50 parts Reagent A with 1 part Reagent B (ie. 50 ml Reagent A plus 1 ml Reagent B)
  5. Prepare your Microplate
    1. Pipette 25 µl of each standard or unknown sample replicate into the designated microplate well
    2. Add 200 µl of the WR to each well and mix plate thoroughly on a plate shaker for 30 seconds
    3. Incubate plate at 37C for 30 minutes
    4. Remove plate and measure the absorbance at 562 nm on a plate reader
    5. Subtract the average 562 nm absorbance measurement of the Blank standard replicates from the 562 absorbance of al the individual standard and unknown
    6. Prepare a standard curve by plotting the average Blank=corrected 562 nm measurement for each BSA standard vs. its concentration in µg/µl. Use the standard curve to determine the protein concentration of each unknown sample

Re-using standards

  • One way to save time would be to re-use standard samples you had prepared previously. Amanda smith has tested samples that were stored in the fridge (hence no freeze-thaw cycles) for several weeks and they worked the same.


Page set up by Janet 5/2013