Blood Type Lab Report Sherman Chen 3B Introduction: The purpose‚ nature‚ and expected findings of the activity. In this lab activity‚ we were first asked to find the blood types and then count the number of blood cells. In the first part of the lab‚ we had to find the ABO and Rh blood type of four simulated blood samples. We did this by observing the antigen/antibody reaction in each of the four samples of simulated blood; if there was agglutination it meant that was the blood type. In the
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Exploring the diversity‚ abundance‚ and variability of diatom-associated bacteria in the oligotrophic ocean I. Abstract The ecology of diatoms may be better explained by conceptualizing them as composite organisms consisting of the host cell and its bacterial associates. Our previous investigated diatom-bacterial interactions at the single-cell level found that bacterial assemblages varied substantially even among closely related individual host cells. The bacterial assemblages associated with single
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High or Low Blood Pressure? Purpose: The purpose of this experiment is to compare blood pressure as related to gender and athletic status. Hypothesis: I predict that males have a higher blood pressure than women and athletes have a higher blood pressure than non athletes Background Info: Blood pressure is the amount of force that blood pushes against the inside walls of blood vessels as it passes through. This pressure
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Lab 11 Methodology By using aseptic‚ a little cultured bacteria was inoculated on the TSA agar. A quadric streak was making. Inoculation loop was heated and keep it cold for a while before the next quadratic streak. Six agar plates were observed for 24 hour at temperature of 30ºC. Choose one from the dense colony and make a sub-culture on the new agar plate. The step was repeated to get a single colony‚ which is pure colony. a) Sequestration of bacteria from fish organs Methodology
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The human blood buffer response to increased amounts of acids and bases was determined by titration of a 25.00 mL sample of H2PO4 buffer solution with 0.1 M HCl and 0.1 M NaOH. The volume of 0.1 M HCl is about double of the amount 0.1 M NaOH used to lower/raise the pH of a blood buffer. In this experiment‚ HCl (a strong acid) and NaOH (a strong base) are used as examples of strong acids/bases‚ and the titration with H2PO4 shows the effect on a buffer solution. The assumption was the addition
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Microbiology Laboratory Report Identification of Unknown Bacteria 03/10/05- 04/01/05 Authors: Richard Hendricks‚ Jessica Prebish; NMU Abstract: Broth culture 16 was randomly selected by our group and subjected to qualitative tests for taxonomic identification. The culture did appear homogenous throughout the testing period and is currently retained by Northern Michigan University’s department of Microbiology. We suggest that culture 16 is an example of Escherichia coli. Background: Techniques
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Reyes Mykee Domingo Aaron Santos Ralph Reyes LBYMATB V26B Report Title Of Activity: Yogurt Making Date Performed: October 4‚ 2012 I. Introduction Last October 4‚ the group performed an activity that involved making our own yogurt. The group prepared the materials and followed the procedures to make the said yogurt. In the activity paper that was given‚ it dictated that during the yogurt making process‚ the bacteria underwent fermentation. “Fermentation is any process where microorganisms
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Introduction: During this unknown lab report various test were performed to differentiate microbes from each other and to compare metabolic and biochemical process. The gram stain distinguishes between Gram positive and Gram negative bacteria based on the composition of the cell wall. The Gram stain procedure distinguishes between Gram positive and Gram negative groups by coloring these cells red or violet. Gram positive bacteria stain violet due to the presence of a thick layer of peptidoglycan
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LAB REPORT NUMBER TWO DATE: 3/25/2010 inal attachment Lab Experiment number 11 PURPOSE: To learn the Gram stain technique‚ the reason for the stain‚ and how to identify the results of the organisms stained. MATERIALS: Bunsen burner‚ inoculating loop‚ staining tray‚ glass slides‚ bibulous paper‚ lens paper‚ oil‚ and microscope METHODS: Apply Crystal Violet (Primary stain) for 1 minute. Rinse with D-water Apply Iodine (Mordant) for 1 minute. Rinse with D-water. Apply Alcohol (Decolorize) for
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Glowing Bacteria Lab Introduction- 1. Transformation involves the transfer of genetic information into a cell by directly taking up foreign DNA from its surroundings. This DNA is then incorporated into the host cell’s own DNA. This transformation usually occurs within plasmids‚ small circular DNA molecules separate from its chromosome. After the recipient cell is infected with the DNA‚ the cell will move on with replication‚ producing offspring with traits encoded by the plasmid. These plasmids
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