Please provide a detailed solution for the following question You have constructed a standard curve from BSA protein for a Bradford Assay. The curve has 0, 1, 2, 3, and 4 ug protein in 50 µl water. You have an unknown protein with a concentration somewhere between 1-5 mg/mL. What serial dilution series should you use to guarantee at least two dilutions of your unknown fall below 3 ug (linear portion) on the standard curve? For example, would 1/2 x 1/2 x 1/2 (3 2-fold dilutions) be sufficiently dilute that two of the dilutions would give values within the linear portion of the standard curve?
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- You are given a container with Na3PO3 that is reportedly contaminated. You are asked by your supervisor to determine the percent purity of that sample in order to know the next measures to be taken by the plant. The following are the procedures that you need to do: a. Dissolve sample weighing 1 g in 35 mL water. b. Prepare solution with 45 mL 3% w/v HgCl2, 30 mL 10% w/v C2H3NaO2 and 10 mL CH3COOH. c. Digest sample then filter then rinse the precipitate that weighs 0.2857 g. d. Compute for the % purity.If pH (± 0.5 pH units) strips were used to determine the equivalence point at pH=8.5. What is the relative error (%) in pH at the equivalence point? I assumed it should be 0.5/8.5 * 100 = 5.88, rounded to 5.9 for sig figs. but I got the answer wrong. Please help and let me know how to solve this.FT-IR technique can be utilized for the analysis of unknown analytes by matching it with__________. Both choices are correct Commercial library/database Reference standard
- Use the following information collected from a SIZE-EXCLUSION CHROMATOGRAPHY experiment to answer the questions below. MW Standards Molecular Weight (kDa) Elution Volume (mL) blue dextran 1000 85 myoglobin 17.2 200 TIM 53.3 178 hemoglobin 62.2 156 IgG 140 122 ATCase 307.9 94 Prepare a graph showing the linear relationship between log function of molecular weight against Ve/Vo. The R2value must be 0.9 or higher. What is the linear equation from the standards given? What is the R2value?if you perform QC for sodium on a chemistry analyzer and the value is greater than 2SD above the mean. This is the second day that this level of control has been >2SD for that analyte. You mixed the vial and repeated. QC was still "out". It is time to troubleshoot. What do you do?An HPLC method was developed for the separation and determination of ibuprofen in blood samples. A 3.00 mL blood sample dissolved in 70.00 mL solvent was prepared and 10.0 mL was injected into the HPLC. Standard ibuprofen solutions were also run.Calculate the ibuprofen present in the 3.00 mL blood sample The following data were obtained. Table po itoo: Ibuprofen concentration, mg/ml0.50 1.0 2.0 3.0 Blood sample Peak area (Right column)5.29.617.419.911.4
- You are provided with a stock standard with a concentration of 100 mg/L, and a solution of unknown concentration. Prepare calibration standards using a 10 mL volumetric flask and a 1 mL piston pipette, and measure on the UV/Vis spectrophotometer (400 nm). Determine the concentration of the unknown after a 1:40 dilution, and provide the concentration of the initial solution. i need to learn how to do the calculations and draw a calibration curve to find concentration of unknown sample after i find the absorbances.Felodipine calcium channel blocker standard (0.251mg/ml) and felodipine sample (0.245mg/ml) solutions were prepared and injected to the HPLC. The peak area of felodipine standard is 275428 and the sample is 272982. The potency (purity) of felodipine standard is 98.9%. What is the assay percentage of felodipine? a. 102.23 b. 98.71 c. 101.07 d. 100.42Tim is interested in analyzing for Pyraclostrobin (pesticide) in strawberries using QuECHers method for extraction and clean up before analysis with HPLC-uv. The concentration of the Pyraclostrobin in the fruits that he sampled is thought to be between 1-10 ng pesticide per g fruit fresh weight. The HPLC-uv instrument he is using has a LoQ of 5 ppb for Pyraclostrobin. Tim is starting out with 500 mg of the sliced fruit
- Methodology: Make schematic diagram for the procedure below B. % SO3 determination Dry the soluble sulfate sample at 100° C for 1-2 hours, and cool in desiccator. Weigh out 0.5 – 0.7 g (± 0.3 mg) duplicates sample. Transfer to 400-mL beakers. Dissolve each in 200 mL of dist. H2O + 4 mL of 6 m HCl. Precipitant is prepared by dissolving 1.3 g BaCl2 ∙ H2O in 100 mL water. Filter if solution is not perfectly clear. Heat the BaCl2 solution and sulfate sample solution nearly to boiling, and then add the entire amount to the HOT sulfate sample solution while stirring vigorously. Wash stirring rod with distilled water and include washings in your final mixture. Digest by letting stand 1-2 hours. Overnight standing is acceptable. Filter through an ash less filter paper of fine porosity (Whatman no. 42). Slowly pour the supernatant liquid through the filter paper.How would i perform a serial dilution of 1/2 and 1/4 if i have 7.5mL of an unknown protein, the final volume is 0.5mL and the known protein standard is 100 microgram/mL?A 10 ml of ascorbic acid (MW=176.1) injection was transferred to a 100 ml volumetric flask and made up to volume with deionized water. A 20 ml of the diluted injection was transferred to a conical flask and titrated with Iodine VS using starch mucilage as the indicator. The iodine solution was standardized against a solution of sodium thiosulfate primary standard (MW=248.2). Results: Weight of sodium thiosulfate used to prepare 100 mL primary standard solution = 2.501 g Volume of thiosulfate solution required to titrate 25 mL of Iodine solution = 24.83 mL Volume of iodine solution required to titrate 20 mL of the diluted ascorbic acid injection = 21.55 mL Stated content of the injection = 10% w/v Calculate the % of the stated content in the injection. (Round-off your answer to 2-decimal places) Answer = ____%