Prepare 100ml of TBST using 10% Tween 20 and 10x PBS (Final 1x PBS and 0.05% Tween 20). Could you please show and explain the calculations?
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- (MB = methylene blue) What is the concentration of the sample of the substance with the reporter absorbance of 0.40 at 595 nm?2 a. You are trying to purify protein C from a mixture of proteins noted in the above Table. If you had only one type of column to choose from, which one would allow you to purify protein C with the least number of contaminants? Size exclusion column Ion exchange column Affinity chromatography using glucose as the bait Affinity chromatography using NAD as the bait Please explain why you chose the column above based upon the properties of the column AND the proteins in the Table.2. For the serial dilution, your stock solution must have a concentration of 3.5 mg/mL. How much diluent must be added to the 5.3 mg/mL red cell to prepare the stock solution? Show pertinent solution/s. How much of the diluent must be added to tube 2 if 200uL Red cell suspension is added? Show pertinent solutions. What are the initial concentrations used for tubes 3, 5, and 6? Show pertinent solutions.
- 3. How many milliliters would you need to prepare a 10-2 dilution from a 10ml starting culture?1. When can gelatin be utilized in culture media preparation? 2. Why should Erlenmeyer flasks hold not more than 60% of their capacity? 3. Why is a lower concentration of NaOH or HCl used for titration while a solution with higher concentration is used for adjusting the pH of the remaining medium?2. During digestion, what happened to the sample analyte during this process? Provide the chemical reaction if possible. 3. On the analysis, what is the importance of calibrating the machine? What happened to the analyte during the analysis of AAS?
- 1. What volume of sterile water for injection (diluent) must be added to reconstitue the powder? 2. How many mL of the reconstituted cefazolin is needed to prepare the final product?6. Using a balance with a sensitivity of 4 mg, an acceptable weighing error of 5% and cherry syrup as the solvent for tartar emetic, how could you obtain the correct quantity of tartar emetic to fill the prescription?1. In the preparation of the standard curve for protein analysis, 50 mnBSA (bovine serum albumin) dissolved in H2O to a final volume of 5mL was used as stock solution. What is the weight of BSA in 0.1 mL ofstock solution? In 0.2 mL? The mentioned aliquots (#9) which were diluted with enough water to a final volume of 1 mL were assayed colorimetrically and yielded the following absorbance readings: mL stock mL H2O Absorbance0.2 0.8 0.1000.4 0.6 0.2000.6 0.4 0.3000.8 0.2 0.4001.0 0.0 0.500 i. Tabulate mg BSA vs. absorbance readingii. Draw the curve where mg BSA is on x-axis and absorbance ony-axis (use graphing paper).iii. Calculate the slope of the curveiv. If a sample solution has an absorbance of 0.332, determinemg protein of the sample.
- 3. Discuss the advantage and disadvantage of Wijs method of iodine value determination. What non-titrimetric method can be used to determine the iodine value of edible oil? Discuss its basic principles and general methods involved.The diffusivity of amino acids in polyacrylamide gel is approximately 1x10^-9 cm2./s calculate the initial flux of amino acids, give an instantaneous gradient of (20g/cm 3 )/8cm Why is polyacrylamide gel is used in electrophoresis?3. Calculate the total volume of the diluent that you are going to use if you have prepared a 3% red cell suspension using 0.5 mL of pRBC.