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- https://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 pleaseFluorescence in-situ hybridisation (FISH) analysis can be performed on fixed pathological tumour sections. Briefly outline why interphase FISH is used on fixed material from a solid tumour, rather than metaphase FISHA 47-year-old obese female complains of pain in her right wrist, with tingling and numbness in the thumb and index and middle fingers for the past 2 weeks. She has been frustrated because the pain causes her to drop her hair-styling tools. A. What are possible 5 differential diagnosis for this case and why? B. What diagnostic testing would support this diagnoses and why? Need detailed answer of both subparts Don't copy from cheggg or internet I match ur answer line If your answer matched I write plagraise answer in comment box
- The following three questions are related to this patient scenario: A 65-year-old male HIV patient is using continuous intravenous (IV) antibiotic infusion to manage a kidney infection and he develops a 103° F fever. Cultures of blood, the IV needle tip, and the insertion site revealed large round cells that reproduced by budding. a. What is your preliminary identification of the infecting organism? b. How might the antibiotic treatment have affected this patient? c. What do the findings suggest about the cause of the fever?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 .…I AM TRYING TO IDENTIFY THIS UNKNOWN. IMAGE 1 HAS TWO PICTURE OF CATALASE TEST AND BLOOD AGAR TEST. I BELIEVED THAT THIS IS " S. PYOGENES. SO I DID A BACITRACIN TEST ON IT. IMAGE 2 SHOWS BACITRACIN TEST IMAGE. ** PLEASE HELP ME IDENTIFY IF THIS IS S. PROGENES AFTER LOOKING AT ALL THE THREE. BACITRACIN SHOULD BE THE CONFIRMATION TEST. IF YOU THINK THAT THIS IS S. PYOGENES AFTER LOOKING AT THE BACITRACIN TEST, THEN PLEAE EXPLAIN HOW DID YOU FIGURE IT OUT FROM THE CONFIRMATION THAT THIS IS S. PYOGENESE FROM BACITRACIN TEST. NEED VALID REASON WHY YOU BELIEVE IT IS S. PYOGENES
- B ut of 1 e flag us page In Canada, facilities that participate in sterile compounding follow guidelines provided by USP Chapter , NAPRA and this professional association: Select one: O a. CAPT Q b. CPTEA O C. FDA O d. CSHP FS Q Search F6 - F7 F8 L F9 m |--- ■■■ 8 + Time left 21:19: F10 Next pageMany ELISAs that are used to identify the presence of antibody to viruses have a 3rd control (along with negative and positive). In between the rows of wells coated with antigen, are rows of cells coated with tissue culture used to grow the virus. In other words, patient serum is added to wells that contain antigen along with wells that contain tissue culture. Why do you think this might be necessary?The plaque assay plate below was made from a dilution of 10-7 and 0.1 ml of the dilution was plated on the cell monolayer. What is the virus titer in PFU/ml? Note: 10e1 means 10 to the first power, etc. Select all answers that apply.
- This is homework not a test! From NTSA case study https://static.nsta.org/case_study_docs/case_studies/cystic_fibrosis.pdf Please help with questions 2, 3 and 4 of part four 2. "The successful use of gene therapy to cure SCID syndrome (2000) is hoped to be a permanent cure for those patients because a good copy of the problem gene was inserted into the patients' blood stem cells in the bone marrow (hematopoietic stem cells). Once white blood cells enter the blood stream they have a limited life span, on the order of a few week to months. The blood stem cells are the cells that create more white blood cells to replace those that are lost. If the gene was only inserted into the circulating mature white blood cells, the patient would only be temporarily cured until those cells were used up or died." The current gene therapy approaches to cure CF involve inserting a functional CFTR gene into the mature epithelial cells of the lungs. In light of the preceding paragraph, do you think that…hi, can I please get help on a case study on nueroanatomy I have been struggling for a couple of hours now and can't seem to understand the study to answer the following questions. is there any way or format that i can get help. I would really appreciate it. thanks! 1. Based on the information in the case, what is the most likely neuroanatomic location for a single lesion that can explain all of the patient’s symptoms and signs? In your own words, explain how you arrived at that localization. 2.What are some possibilities for the nature of the lesion (e.g., stroke, tumor, trauma, etc.)? In your own words, explain your rationale for these options. 3. How does the laboratory data and neuroimaging demonstrate the actual lesion for the patient? Describe how you interpret the data in your own words. 4.How was the patient was treated, and how did they subsequently fare? Describe the treatment plan in your own words.A researcher wants to compare the pathogenicity of a mutant pathogen relative to wild type in an animal model. The mutant is marked with the constitutive expression of a foc gene that turns colonies blue on X-gal agar. The input ratio of the experiment Dilue/white colonies) was 10:1. The output ratio of the infection experiment tant to d type was 1-100 a. What is the CI? Show your work. 1. Define the Cr and describe what it measures in your answer Which of these genotypes does better during infection, the mutant or the wild-type?