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- Following is the data and notice that it is a terrible idea to culture hMSCs longer than 10 days. You’re strongly Days # cells0 50001 75002 125003 125004 218005 287006 530007 1143008 1653009 19200010 19200011 11680012 8950013 8830014 78300 Part1 You are working for a start-up that is pursuing a clinical trial. The trial involves grafting hMSCs intopatients suffering from interveterbral disc disease using a degradable polymer scaffold. You are going to 3Dprint a porous cylindrical scaffold that is 2 cm in radius and 1 cm in height (matching the dimensions of adegenerated disc). Assume a porosity of 50%. You will fill available volume of the scaffold with hMSCs at adensity of 1 million cells per cm3. Based on the data above, what starting number of cells will you use andhow long will it take you to get enough cells for the trial? Part2The trial is a failure (patients did not report any reduction in back pain). Your team wants to try againusing 85% hMSCs and 15% nucleus pulposus cells .…Explain the two major drawbacks of phenotypic testing methods that require culturing the pathogen.Write a detailed description of the following plate 1- blood Agar plate 2-PEa Agar Plate
- Topic: Stoma bag. Give in points and easily understand and also a picture of it in wad hospital. What is Stoma Bag? What happens if didn't treat it? How to detect? Example picture stoma bag in a wad? How did it happen? Plan care nursing for stoma bag? anything related to the stoma bag? effect? diagnosis?has been testing many observations is incorrectDiscuss either (a) how allelopathy contributes to the invasiveness of spotted knapweed or (b) the difference between choice and non-choice experiments and how it relates to experiments on hyperaccumulating plants.
- Define the two major drawbacks of phenotypic testing methods that require culturing the pathogen.10:33 , O a 85%I AIATS For Two Year Medic. A 114 /180 (02:51 hr min Mark for Review The chemical substance involved in growth inhibiting activities, is АВА Auxin Gibberellin Ethylene Clear Response IIhttps://youtu.be/w7aIxiZQ60g Multiplexing agglutination https://youtu.be/uWStmyJ5Qc0 This is the multiplexing agglutination. Lab report I don’t really know what to talk about, the data, conclusions and the purpose of this. Need help please
- Discuss the difference between the nontreponemal agglutination test and the treponemal agglutination test. pls make it organize and if possible do it in table form to really show the difference, but if not just make it comprehensive and detailPhytomenadione MEDICATION IN EACH CATEGORY OF DRUGS AND APPLY THE 10 R’S TO MEDICATION Fill out all the the blanks in the table below. CATEGORY 2 : DRUGS USED FOR PEDIA PATIENTS ( Phytomenadione) 10 R’s TO MEDICATION BRIEF DISCUSSION OF EACH OF THE 10R’s TO MEDICATION APPLICATION (Phytomenadione) 1. RIGHT DRUG (Phytomenadione) 2. RIGHT DOSE 3. RIGHT TIME 4. RIGHT ROUTE 5. RIGHT PATIENT 6. RIGHT TO EDUCATE 7. RIGHT TO REFUSE 8. RIGHT ASSESSMENT 9. RIGHT EVALUATION 10. RIGHT DOCUMENTATIONt/Root/Pages/TestTaker/MonitorLaunch.aspx?id%3DE9B80AE3-962E-4628-B79D-A3F06F1CAB72 MonitorLaunchaspx?id%3DE9B80AE3-962E-4628-879D-A3F0EFICABT2-Google Chrone uninoculated tube The medium shown here was inoculated with a bacterium then incubated for 48 hours; an uninoculated control tube is also present for comparison. This particular bacterium gave a for this test. a) O negative result b) O positive result c) O indeterminate result Review Later d) O variable result