bacterial inhibitors abolish the most bacteria. In the future‚ people will choose the most effective bacterial inhibitor; therefore‚ they save both money and time. If the disinfectants are applied to the bacteria‚ then the zone of inhibition will increase because disinfectants are antimicrobial agents that are applied to non-living objects‚ and a petri dish is a nonliving
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Life Science Lab. A. Arnold Tuesdays @ 2:30 September 30th‚ 2011 Lab Report: Nuclear and Cell Division. PART A: Stages of Mitosis in my own words. 1. Interphase: DNA has formed already‚ but it remains in the simple form of chromatin. Chromatins are structures that are loosely coiled in the cell.3 I also observed during my lab that this was the only stage where I could still see a nucleus and nucleolus intact within the cell; this is because it’s the only stage where the nuclear membrane has
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Lab report for Experiment #2: Extraction Your Name: Name of TA: Lab Partner’s Name: Lab Section: Title: Experiment #2: Extraction Purpose: What is the purpose of this lab? In your OWN words! Observations: Weighed out 3.2568 grams of chemical mixture that was yellow in color. Dissolved dry chemicals in 38 ml CH2Cl2 with gentle heating. Poured the yellow solution into sep funnel. Added 10 ml CH2Cl2 to flask to rinse‚ poured solution into sep funnel. Added 15 ml 3 M
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the bacteria are unable to convert squalane into squalene for use in the hopanoid biosynthesis pathway. Another possibility is that the bacteria are using other materials than squalane as a preferred substrate in this pathway‚ as they would require less energy to convert into the necessary compounds. Despite the lack of temperature-dependent effects‚ the consistent significant increase in growth in samples treated with squalane indicates that this compound provides some benefit to the bacteria. In
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this lab was to determine the density of water and an unknown liquid. Density is defined as the mass of a substance divided by its volume. It is an intrinsive property of matter and is used to specifically characterize substances. III. Procedure: 1.We massed an empty 10mL graduated cylinder to the nearest .01g. 2.Then‚ we filled the graduated cylinder with 4.0-5.0 mL of distilled water‚ 3.massed it to the nearest 0.1 ml and 4. recorded the data. Then to determine the density of the unknown liquid;
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Introduction When plant and animal cells are placed in a hypotonic environment‚ osmosis will occur. The structure of these cells determines the response to the difference in gradient‚ whether this be lysis (the explosion of cells due to the sudden increase in water pressure within the cell) in animal cells or turgor pressure (the pressure created by the increase in water pressure within the cell) in plant cells. Turgor pressure prevents further osmosis‚ which causes the water potential outside the
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September 23‚ 2012 Introduction: Bacteria are everywhere. Some can be seen with the naked eye and some require a microscope but how do we distinguish one kind of bacteria from another? To answer this question‚ we were required to complete three bacterial labs that helped us to understand what microorganisms are and how to identify and classify them. Thus‚ the main purpose of this project is to identify our unknown microorganisms‚ more specifically‚ our unknown bacteria. There are many ways to distinguish
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’Neil 2002). The particular conditions that had to exist for this to apply were that the population had no mutation‚ had no natural selection‚ was a large population‚ had only random mating‚ and had no migration. For the cases to follow later in the lab‚ Cases 1 and 2 exemplify Hardy-Weinberg conditions. All of the others either have selection or not enough members in the population‚ which will be the most-closely observed
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1. Introduction Microscopy is an essential technique not only in cell biology but natural science as a whole. We compared different types of microscopic techniques ‚ according to the specimen used and the scope of the experiment. Two specimens‚ stained and unstained‚ containing CHO cells‚ were prepared‚ examined and analyzed under the microscope using bright field (HF)‚ dark field (DF) and phase contrast (PH) settings. In addition‚ the four phases of cell division cycle were estimated.. Bright
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Evolution Lab Report Marcos Chapa July 3‚ 2013 BIO 101 Rebecca Avants The purpose of the lab I have conducted is to analyze how altering the finch’s environment would affect the evolution of the finches by isolating each population of finches from each other‚ placing them each on a different island. This influence on the species by the environment is called allopatric speciation. One population of the finches that are located Darwin Island‚ which is 1 km‚ and the other population of finches
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