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- Types of specimens are given. Match the following to their advantage. A. Less contaminated by bacteria B. No interference C. Assurance of unadulterated specimen based on its temperature D. Better understanding on glucose metabolism E. Does not contain CHO metabolites F. Concentrated G. Collected as needed H. Sterile specimen from a child 1. Midstream Clean Catch 2. Random 3. Drug specimen collection 4. 8-hour specimen 5. Glucose tolerance 6. Pediatric 7.FastingWhat is the clinical significance of ESR determination? Differentiate Wintrobe from Westergreen regarding accuracy of the test in a tabulated order. NOTE: Kindly asnwer all the questions. Thank you!1) Determine the MICS on the simulated microbroth-dilution results from an MIC Assay on Staphylococcus aureus. Legends: PC: Positive Control (No antimicrobial agent) NC: Negative Control (No bacteria) No Growth With Growth µg/mL: 128 64 32 16 8 4 2 1 0.5 0.25 PC NC 2 3 4 5 7 8 9 10 11 12 Amoxicillin A Ticarcillin Piperacillin C D Cefotaxime E Ertapenem F Nalidixic Acid G Ciprofloxacin H Gentamicin а. Fill out the MICS on the table below. MIC Susceptibility to Staphylococcus aureus Antimicrobial Agent (Hg/mL) (Susceptible, Intermediate, or Resistant) Amoxicillin Ticarcillin Piperacillin Cefotaxime Ertapenem Nalidixic Acid Ciprofloxacin Gentamicin B
- Answer the following questions: Therapeutic Classification of Sweet Orange Peel Tincture, USP Indication of Sweet Orange Peel Tincture, USPAnalysis of the pathological constituents GIVE THE FOLLOWING: a. Name of Test/Test Reagent b. Positive Result Blood (Note: Presence of blood in urine is termed as hemolobinuria) To 1 ml of freshly prepared Benzidine solution (sat’d sol’n of Benzidine in glacial Acetic acid) and 10 drops of urine sample. Add 5 drops of 3% H2O2. A positive result is indicated by a blue green color.Brown algal natural products have been used as chemotaxonomic markers (true or false)
- Think of another type of test to determine whrther a person is lactase persistent or nonpersistent. Describe idea in one or two sentences.Cells were incubated with chloroquine for 2 hours before stimulation with lipopolysaccharide (LPS, 1g/ml). Cell viability was measured by staining cells with 3-(4,5-dimethylthiazol-2- yl)-2,5- diphenyltetrazolium bromide. TNF in the culture supernatant and the cell lysate were measured by sandwich ELISA, using specific monoclonal antibodies according to the manufacturer's instructions. To determine the level of cell-associated cytokines, cells were washed with phosphate-buffered saline (PBS) and lysed in a buffer containing 0.5% NP-40. Standard recombinant proteins were also diluted in PBS containing the same concentrations of NP-40 as the cell lysate. Cytokine synthesized were proteolytically cleaved and released into medium. The amount of cytokines in the culture supernatant and the cell lysate were presented. Results for TNF production are shown in Figure1 (Jang et al, 2006). (Cells : PBMC: Human peripheral blood mononuclear cells, monocytes, monocytic lymphoma U-937 and leukemia…Order: metoclopramide 5 mg PO Q6HPatient 30 kg; 3 years oldSupply: 5 mg/5 mLLiterature: 0.1 to 0.2 mg/kg/dose up to four times per day Order: cefotaxime (Claraforan) 0.5 g IM Q6HPatient: 48 lbSupply: 300 mg/ reconstituted solutionLiterature: 100 to 200 mg/kg/day divided Q6H
- Cells were incubated with chloroquine for 2 hours before stimulation with lipopolysaccharide (LPS, lg/ml). Cell viability was measured by staining cells with 3-(4,5-dimethylthiazol-2- yl)-2,5- diphenyltetrazolium bromide. TNF in the culture supernatant and the cell lysate were measured by sandwich ELISA, using specific monoclonal antibodies according to the manufacturer's instructions. To determine the level of cell-associated cytokines, cells were washed with phosphate-buffered saline (PBS) and lysed in a buffer containing 0.5% NP-40. Standard recombinant proteins were also diluted in PBS containing the same concentrations of NP-40 as the cell lysate. Cytokine synthesized were proteolytically cleaved and released into medium. The amount of cytokines in the culture supernatant and the cell lysate were presented. Results for TNF production are shown in Figure 1 (Jang et al, 2006). (Cells : PBMC: Human peripheral blood mononuclear cells, monocytes, monocytic lymphoma U-937 and leukemia…Cyanocobalamin injection to start on Sunday 1000 mcg intramuscularly once a day for 7 days, 1000 mcg intramuscularly once every other day for 7 days, then once every 4 days for another 2 to 3 weeks is recommended. How many mcg are required for a 4 week treatment?State the difference between reducing and non-reducing sugars. Give one test to show the difference between reducing and non-reducing sugars. (Give the indication of positive test, such as color, precipitate formation, etc.)