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According to question we know the formula for calculating the concentration of protein by taking the reference BSA we generally use the following formula
y= 0.052(X) - 0.120 |
Now, we have to find the “x” value
X for concentration of unknown sample (protein) in mg/ml
y= 0.052 X - 0.120
0.052 X=y+0.120
X=y+0.120/0.052
Here, y=0.5
X=0.5+0.120/0.052
X=0.5+2.307
X=2.807 mg/ml(concentration of protein) |
The following curve presents the relationship between BSA concentration and OD at 595 or 600 nm....
I forgot to put down that the observance (=OD) at 280nm is 0.679A Experiment 8: Bradford assay and UV-method for determination of protein concentrations Materials - An ice bucket with ice, your purified sample, three visible plastic cuvettes for Bradford assay, one UV plastic cuvette for UV-method, a piece of parafilm, a Vis-spec, a Lab Quest, Bradford reagent, white tape (share), a sharpie. Bradford assay (reference 21) 1. Add 990 uk Bradford assay reagent to a plastic cuvette 2. Blank...
1. You have generated the following standard curve after a Bradford Assay to measure Absorbance vs samples of known BSA concentrations. Now you need to determine the amount of protein in two mitochondria samples taken from fish, one taken from fish under normal conditions and the other taken from fish under oxidative stress. The absorbance reading for the normal fish fraction was A595=175, and the absorbance reading for the stressed fish fraction was A595= 275 Bradford Assay Standard Curve y...
4) You have been given the job of designing an experiment to test the effects of an inhibitor on the coronavirus polymerase. Assume you have a stock solution containing purified polymerase protein. You want to know how much polymerase protein you have in the stock solution. To do this, you will use the Bradford Assay. If you mix 50L of polymerase protein stock solution with 100L of water, perform the Bradford Assays and get a resulting OD 595mm of 0.6,...