Name : Terry-Ann Poorman Id# : 27120454 Lab# : 1 Lab Instructor: Mrs. Bryan Title : Aim : Discussion Questions: 1) What are the types of urine specimens? Random specimen This type of specimen is used for microscopic and chemical analysis. As the name suggest this sample can be a randomly collected specimen and at an unspecified times. This is often more convenient for the patient. A random specimen is suitable for most screening purposes. Random specimens can at times give an inaccurate view of a patient's health, this can be due to whether the specimen is too diluted and analytic values are unnatural. Being that there aren’t any precise method for how the collection of this specimen should be carried out, avoiding the introduction of contaminants …show more content…
Pediatric specimens This is a sterile specimen can be retrieved by catheterization or suprapubic aspiration. The specimen can be collected by fixing a soft, clear plastic bag with adhesive to the general area of both boys and girls. Catheterized specimen This specimen is collected under sterile conditions where a hollow tube is passed through the urethra into the bladder. Midstream “clean catch” specimen The reduced incidence of cellular and microbial contamination causes midstream urine to be the preferred specimen for culture and sensitivity testing. Patients should first cleanse the urethral area and void the first portion of urine in the toilet. This reduces the incidence of contamination of the urine specimen. This method can be carried out anytime, whether day or night. 2) List the different urine preservatives and the advantages and disadvantages of each. • Refrigeration Advantages: Doesn't interfere with chemical tests Disadvantages: 1) raises specific gravity by hydrometer 2) Precipitates amorphous phosphates and urates. 3) Prevents bacterial growth for only 24hrs • Saccomanno fixative Advantages: 1) preserves cellular
The last step of dissection made them trace the vas deferens to the urinary bladder. As a final step to the whole lab, the lab groups then removed all dissection pins, cleaned the dissection tools, placed the Neovison vison in a
During my clinical preceptorship at New York Presbyterian Hospital, many patients that came into the hospital with urinary retention a catheter was inserted to determine the amount of urine in their bladder or post-void residual (PVR). Many patients later developed pain and a urinary tract infection or Community Acquired Infection secondary to frequent cauterization. Therefore, the gap identified was related to a knowledge deficit of the current practice that inserting a
Unknown Lab Report Unknown # 25 By: Jenna Riordan March 19, 2018 Bio 2843 1. Introduction Microbiology is the study of microorganisms found in all different environments throughout Earth, from the hot thermal vents at the bottom of the ocean to the ice at the top of a mountain.
The Unknown Identification Lab was an experiment that provided the opportunity to apply all the tests that were learned in the semester of lab, to identify the two bacterias that remain unknown. Gram- staining and two other tests will be used to identify the unknowns. This experiment is crucial to the understanding of each test, and can benefit in the ability to identify the characteristics of specific bacteria. Having a clearer understanding of the bacteria can further the research of bacteria for medicine, such as antibiotics. The understanding can also help the development of research in the environment.
We hypothesized that men with apparently clinically localized CaP harboring occult metastases would also have elevated plasma levels of components of the uPA system of plasminogen activation that would be associated with a higher risk of biochemical progression despite effective local control of disease. Therefore, to determine the relationship of the major components of the uPA system with established markers of CaP presence, invasion, metastasis, and progression, we studied pre- and postoperative plasma levels of uPA and uPAR in patients with clinically localized CaP who underwent radical prostatectomy, patients with CaP metastases to regional lymph nodes, patients with newly diagnosed CaP metastases to bone, and healthy men. The availability of pre- and
After graphing this data, part two needed to be completed. To start, 5 different test tubes were filled with 3 drops of 5 different patients blood followed by 5 drops of deionized water. Next, 5 drops of Barium Hydroxide was placed in each tube to clear proteins and cell membranes for an accurate reading could be made. Blood Clots also interfere with the readings of glucose, so 1 drop of Heparin was placed in each tube to prevent blood clots. The tubes were mixed and centrifuged.
Elijah Brycth B. Jarlos IX-Argon 1. Multicellularity is a condition of an organism to have multicellular cells. An example of a organism who has multicellular cells are plants, animals, and humans. The main reason of why scientists have a hard time finding a good set of existing organisms to compare. Is neither the first set of organisms which is being compared is dying as fast as the second specimen is being examined or they just can’t find the right species.
The addition signs for each test on serum 2216 illiterates how concentrated the molecule is like purple for example was the most concentrated due to the amount of addition signs in the table. For Macromolecule test 1 and 2 the sample was diluted. Both the concentration and decreased by an equal set of intervals. The volume of distilled water is what was added and the results illustrate how deeply colored each concentration was. Each cup was diluted with the test pertaining to it with a syringe that explain the volume and the concentration is from heating or mixing the sample throughout the investigation.
Tn 4351 was originally isolated from bacteroides fragilis [30] . The transposon was successfully introduced into Cytophaga succinicans, Flavobacterium meningosepticum, Flexibacter canadiansis, Flexibacter strain SFI and Sporocytophaga myxococcoides by conjugation [25]. Tn 4351carries two antibiotic resistance gene. One of the codes for resistance to erythromycin and clindamycin which is expressed in bactroides but not in E.Coli. The other gene codes for resistance in tetracycline and is expressed in aerobically grpwn E. coli, but not in anaerobically grpwn E. coli or in bacteroides.
Leah Romero 10/30/2017 Conclusion Lab 3 Chem 102L In lab 3, fundamentals of chromatography, the purpose was to examine how components of mixtures can be separated by taking advantage of different in physical properties. A huge process in this lab was paper chromatography, which was used to isolate food dyes that are found in different drink mixes. The different chromatograms of FD&C dyes were compared to identify which dyes are present in each of the mixes.
The objective of the sludge lab was to determine how many different pure substances were in the sludge by using the methods and techniques we have learned throughout the year. We had to pick separation methods so we could separate our sludge and then test characteristic properties on our separated liquids and solids. This experiment made us use our knowledge on characteristic properties to pick the ones we should test to help us identify our pure substances. Characteristic properties are properties that help identify a solid or liquid. Each solid or liquid has a certain density, boiling point, solubility, flammability, so if you know what each one is then you can use that information to help you identify your solid or liquid.
One of the most prevalent method being Saliva Drug Test. Saliva provides a non-invasive and quick specimen for drug testing. A Saliva Drug Test ranges from detection of alcohol to cannabis, HIV antibodies to steroids. Saliva Drug Test enables a screening in a very short detection time period. They are designed to tell if someone has recently used a drug.
After a gram stain was done unknown #257 was identified as a gram positive organism because when observed under the microscope the organism appeared purple with cocci in clusters. The organism was also catalase positive which means that it produced enzyme catalase and bubbled when hydrogen peroxide was added to it. Three test were conducted based on the result of the gram staining procedure. Blood agar with a Novobiocin disk was chosen as well as DNase (DNA) and Mannitol Salts (MSA) agar. The Blood agar is a bright red, opaque plate and the streaking or the inoculation technique was a modified streaking for isolation with a heavy quadrant one.
In such cases, the sample can be retrieved by aspiration with another needle or picked up with a fine wooden stick or by tapping the hub against the slide.
Then the last alternative form of animal testing is microdosing. Microdosing involves minuscule amounts of a test substance are given to human volunteers so researchers can track how said