Paul.xu at 16:13, 22 January 2017

2017-01-22T16:13:45Z

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'''Bradford Reagent (5X concentrate)'''

100 mg     Coomassie Brilliant Blue G-250 47 ml         Methanol (100%) 100 ml     Phosphoric Acid (85%) QS to 200 ml with H2O

•    NOTE: Coomassie must be dissolved in the methanol FIRST before the other ingredients are added.

For protein concentration analysis •    The BioRad protein assay reagent is the same as the Bradford reagent so we make our own instead of busying it and it works just as well •    We cut all our volumes in half so use 50 μl of protein dilution and 2.5 ml of Bradford reagent •    I usually choose 5 μl of protein sample diluted in 45 μl of water as a starting point because my yields are usually pretty good •    We use a 1 mg/ml BSA solution for our standard •    I have set up an Excel spreadsheet to determine the concentration from the absorbance

Sample set-up:

Sample    Protein    Water    Bradford reagent Blank    0 μl    50 μl    2.5 ml 0.2 mg/ml BSA    10 μl    40 μl    2.5 ml 0.4 mg/ml BSA    20 μl    30 μl    2.5 ml 0.6 mg/ml BSA    30 μl    20 μl    2.5 ml 0.8 mg/ml BSA    40 μl    10 μl    2.5 ml Sample 1    5 μl    45 μl    2.5 ml Sample 2    5 μl    45 μl    2.5 ml Sample 3     5 μl    45 μl    2.5 ml

For Excel Spreadsheet:

DF  is the dilution factor of your lysate (i.e. 5 μL of lysate would be a DF of 10) Conc (mg/ml) is the concentration of the diluted sample T Conc (mg/ml) is the concentration of your lysate μl/20 μg and μl/50 μg is the amount of lysate needed for 20 μg and 50 μg of protein repectively

The spreadsheet is set up so that all you have to do is enter the Abs values for your standards and the Abs and DF values for your samples, then it will calculate the rest.
[[Category:Buffer Recipe]]
== Incompatible Substances /Amount Compatible ==

The concentration listed below is the maximum amount of material which can be present in the protein sample without causing interference in the standard protocol when 20 ul protein sample is used for Bradford assay.

 '''Buffer Systems''' ACES, pH 7.8 100 mM N-Acetylglucosamine in PBS, pH 7.2, 100 mM Bicine, pH 8.4 100 mM Bis-Tris, pH 6.5 100 mM Calcium chloride in TBS, pH 7.2 10 mM CelLytic B Reagent undiluted, no interference CHES, pH 9.0 100 mM Cobalt chloride in TBS, pH 7.2 10 mM EPPS, pH 8.0 100 mM Ferric chloride in TBS, pH 7.2 10 mM Glycine 100 mM HEPES, pH 7.5 100 mM Imidazole, pH 7.0 200 mM MES (0.1 M), NaCl (0.9%), pH 4.7 undiluted MES, pH 6.1 100 mM MOPS, pH 7.2 100 mM Nickel chloride in TBS, pH 7.2 10 mM PBS; Phosphate (0.1 M), NaCl (0.15 M), pH 7.2, undiluted PIPES, pH 6.8 100 mM Sodium acetate, pH 4.8 180 mM Sodium bicarbonate 0.1 M Sodium citrate, pH 4.8 or pH 6.4 200 mM Sodium Citrate (0.6 M), MOPS (0.1 M), pH 7.5, undiluted Sodium phosphate 0.1 M TBS; Tris (25 mM), NaCl (0.15 M), pH 7.6, undiluted Tricine, pH 8.0 100 mM Triethanolamine, pH 7.8 100 mM Tris 2.0 M Tris (25 mM), Glycine (192 mM), pH 8.0, undiluted Tris (25 mM), Glycine (192 mM), SDS (0.1%), pH 8.3, 1:2 dilution Zinc chloride in TBS, pH 7.2 10 mM Buffer Additives Ammonium sulfate 1.0 M Aprotinin 10 mg/L Asparagine 10 mM Cesium bicarbonate 0.1 M Glucose 1.0 M Glycerol 10% Guanidine•HCl 3.5 M Hydrochloric Acid 0.1 M Imidazole, pH 7.0 200 mM Leupeptin 10 mg/L Phenol Red 0.5 mg/ml PMSF 1 mM Sodium azide 0.5% Sodium chloride 5.0 M Sodium Hydroxide 0.1 M  Beyotime Institute of Biotechnology Sodium orthovanadate in PBS, 1 mM Thimerosal 0.01% Sucrose 10% TLCK 0.1 mg/L TPCK 0.1 mg/L Urea 3.0 M 3.0 M Detergents Brij®-35 0.125% Brij®-52 0.031% CHAPS 5% CHAPSO 5% Deoxycholic acid 0.050% Nonidet P-40 (Igepal CA-630) 0.5% N-Tetradecyl-N 0.125% Octyl ®-glucoside 0.5% Octyl ®-thioglucopyranoside 3% SDS 0.125% Span® 20 0.5% Triton® X-100 0.125% Triton® X-114 0.125% Triton® X-305 0.5% Triton® X-405 0.5% Tween® 20 0.062% Tween® 60 0.1% Tween® 80 0.062% Chelating agents EDTA 100 mM 100 mM EGTA 2 mM 2 mM Sodium citrate, pH 4.8 or pH 6.4 200 mM Reducing & Thiol Containing Agents 2-Mercaptoethanol 1.0 M Ascorbic acid 50 mM Cysteine 10 mM Dithioerythritol (DTE) 1 mM Dithiothreitol (DTT) 5 mM Potassium thiocyanate 3.0 M Solvents Acetone 10% Acetonitrile 10% DMF 10% DMSO 10% Ethanol 10% Methanol 10% Note: This is not a complete compatibility chart. There are many substances that can affect different proteins in different ways. One may assay the protein of interest in deionized water alone, then in buffer with possible interfering substances. Comparison of the readings will indicate if an interference exists. Note: Reagents that change the pH of the assay or contains high levels of detergents will interfere with the Bradford assay.

BradFord Assay - Revision history

Paul.xu at 16:13, 22 January 2017