The standard curve of a biuret assay gave the equation: y=0.4193x. The absorbance for Unknown A = 0.098 and Unknown B = 0.325. Are you equally confident in the accuracy of the protein concentrations you would calculate for samples Unknown A and Unknown B? Briefly explain your answer.
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- A spectrophotometric method for the quantitative determination of the concentration ofPb2+ in blood yields an Ssamp of 0.133 for a 1 mL sample of blood that has been diluted to 6 mL. A second sample is spiked with 1 µL of a 1467 ppb Pb2+ standard and diluted to 6 mL, yielding an Sspike of 0.491. Determine the concentration of Pb2+ in the original sample of blood.You obtained the following raw data when setting up a Bradford standard curve: BSA (mg/ml) Absorbancy 595nm 0 0.225 1 0.310 2 0.420 3 0.510 4 0.610 5 0.720 6 0.810 7 0.915 8 0.950 9 0.980 10 0.990 After blanking against a bradford-dH2O sample, the protein concentration of an unknown sample was determined using the same method and an absorbancy of 0.523 was obtained. Set up a standard curve, excluding outliers (experimental and statistical) and determine the protein concentration in the unknown sample in mg / ml (up to 3 significant figures).The predominate form of caffeine at pH 9.4 is neutrally charged. If nitromethane, a compound often used as neutral marker, was added to the sample and standard CE vials, predict the impact on the electropherogram, the peak areas, and the determination of caffeine, aspartame and benzoic acid concentrations?
- You have carried out an experiment using the spectrophotometry concept. A solutioncontaining compound X is mixed with reagent 1 and then reagent 2. This mixture produces ablue colour whose absorbance (A) could be read at 550 nm. The results are shown below If the standard solution (compound X) used have a concentration of 1 mM: 3. If the absorbance was read using 1 cm diameter cuvettes, calculate the molar extinctioncoefficient for compound X in the solution. State the unit for the coefficient. Assumeeach molecule of X produces one molecule of coloured compoundA 5.00-mL sample of blood was treated with trichloroacetic acid to precipitate proteins. After centrifugation, the resulting solution was brought to pH 3 and extracted with two 5-mL portions of methyl isobutyl ketone containing the lead-complexing agent APCD. The extract was aspirated directly into an air/acetylene flame and yielded an absorbance of 0.527 at 283.3 nm. Five-milliliter aliquots of standard solutions containing 0.400 and 0.600 ppm of lead were treated in the same way and yielded absorbances of 0.396 and 0.599. Find the concentration of lead in the sample in ppm assuming that Beer’s law is followed.What are the parameters that can be used for analytes identification and quantification using Cyclic Voltammetry, respectively?
- 1 mL was taken from the sample filtrate and mixed with 13 mL pure water and 4 mL sulfomolybdic acid and 2 mL dilute SnCI2 solution by adding it, and after waiting for 15 minutes, the absorbance of the resulting solutions against pure water was read at 520 nm. if the function of the calibration graph obtained with standard phosphorus solutions of 0.5-2.5 mg/mL is y= 0.245x + 0.107 and the absorbance of the serum sample is 0.342, how many grams of phosphorus is the amount in the sample?A standard curve for glucose analysis was prepared.The slope (m) was found to be 1.341 while the y-intercept (b) was -0.333. Calculate the concentration (x) of glucose having an absorbance (y) of 0.151. 0.067 0.361 0.858 0.136A spectrophotometer method for the quantitative analysis of Pb2+ in blood uses Cu2+ as an internal standard. A standard containing 1.75 ppb Pb2+ and 2.25 ppb Cu2+ yields a signal of 0.832 for Pb2+ and a signal of 0.351 for Cu2+. A sample of blood is spiked with the same concentration of Cu2+, giving a signal of 0.520 for Pb2+ and 0.289 for Cu2+. Determine the concentration of Pb2+ in the sample of blood.
- A spectrophotometric method for the quantitative analysis of Fe2+ in blood uses Zn2+ as an internal standard. A sample containing Fe2+ and Zn2+ with final concentration of 3.25 ppb and 0.75 ppb, respectively, that yields a signal of 0.423 for Fe2+ and 0.650 for Zn2+. Subsequently, a sample of blood is spiked with Zn2+ to give the same final concentration and yielded a signal of 0.832 for Zn2+ and 0.110 for the unknown concentration of Fe2+. Determine the concentration of Fe2+ in the sample of blood.A 5.00-mL sample of blood was treated with trichloroacetic acid to precipitate proteins. After centrifugation, the resulting solution was brought to pH 3 and extracted with two 5-mL portions of methyl isobutyl ketone containing the lead-complexing agent APCD. The extract was aspirated directly into an air/acetylene flame and yielded an absorbance of 0.569 at 283.3 nm. Five-milliliter aliquots of standard solutions containing 0.400 and 0.600 ppm of lead were treated in the same way and yielded absorbances of 0.396 and 0.599. Please calculate the concentration of lead in the sample in ppm.A student weighed out 0.150 g of protein powder and dissolved it in 100 mL of water (Solution 1). The student then diluted this solution by transferring 1 mL into a 25 mL flask and diluting with water (Solution 2). Finally, 1 mL of that solution was transferred to a test tube and combined with 4 mL Bradford reagent. The absorbance of the solution in the test tube was 0.144. Assuming that the best fit linear line of the standard curve was y=0.04144x+0.01521 (μgmL), calculate the percent protein by mass in the original protein powder.