Testing Cell Transportation Across a Membrane Introduction Cells have the amazing ability to transport certain molecules in or out of their membrane. Some require no energy to do so (passive transport) while others require energy to be processed through (active transport). There is also the transportation of water across a membrane‚ which has its own term of osmosis. Too much of something can be taken in‚ or too little enters. This especially happens to plants‚ who require water (and sun) to live
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3.01 Cell Cycle Lab Report Safety Notes: * Always handle microscopes and glass slides carefully. * Wash your hands after handling the prepared specimens. Materials: * Compound light microscope * Glass microscope slide with prepared onion root tip specimen Purpose: * understand and identify the stages of the cell cycle and mitosis. * apply an analytical technique to estimate the relative length of each stage of the cell cycle. Hypothesis Procedure: I predict that
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The Mammalian Heart Analysis Questions 1. The job performed by the atria is collecting blood‚ while the job performed by the ventricles is pumping blood. Since the atria are thin-walled‚ they must function similar to thin bags that collect the blood. The ventricles have thick walls‚ which allow them to contract strongly to be able to pump blood to the rest of the body. 2. The deoxygenated blood must be pumped to the lungs‚ where it becomes oxygenated prior to be being pumped back to the rest
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Topic 6: Mammalian Pheromones Abstract A pheromone is a chemical signal which is released by one animal and received by another‚ which induce a species specific reaction. Pheromones are detected via chemosensory systems known as the Vomeronasal Organ (VNO). Within a wide range of mammals the VNO is used to elicit a generalized sexual response‚ primarily affecting the reproductive tract. This is seen in most terrestrial mammals who have adapted to sensing volatile chemical signals; the Mouse displays
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Epidermis Cells Aim: To see if rhubarb changes when it is placed in solutions of different concentrations. Introduction: "Plasmolysis in Rhubarb Epidermis Cells" is an experiment to see whether or not rhubarb changed its cell structure when placed within different types or solutions. "A single layer of plant cell is placed on a micrscope slide and either distilled water or 5% NaCl solution is added to the cells. Osmosis will occur resulting in either turgid cells or plasmolysed cells." (www
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Kaur Pure Cultures Lab 1/31/13 Introduction : Pure cultures are made of only one type of organisms and can be used to study their properties. A method used to isolate pure cultures is making a steak-plate‚ which is a dilution process in which culture is spread over an agar plate in a certain manner. Using a loop rod‚ culture was taken from the tube and dragged across area 1 several time‚of the agar. The agar was then turned 90º‚ and the loop was flamed and cooled. Taking some culture from area
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bottom with the root cap‚ then the zone of cell division next is the zone of cell elongation‚ and at the top of the root is the zone of differentiation. To figure out what section of the root has the highest number of cells in mitosis we did an experiment where we found out cells that are closer to the root tip are more likely to be doing mitosis than the cells that are further away from the root tip. Through the experiment‚ we looked at the zone of cell division‚ which is
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Erica Osorio 5057497 Christian Roque and Rogerlio The Mechanisms by which E.Coli Cells Developed Immunities toward Ampicillin due to Plasmid and DNA Consumption U34 Abstract During the ampicillin experiment the ability to transform cells to make them adaptable to their environment was studied. The E.coli bacterial cell was used in order to observe how its DNA was able to change and develop immunity towards ampicillin. In order for this change to occur the use of several
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Purpose: Examine the role of the cell membrane in the cell by disrupting its function using temperature (Biology 107 Laboratory Manual 2014). This will improve the general understanding of optimal growing temperatures and the breakdown of the cell membrane Procedure: Betacyanin solution of a known concentration was diluted to create a dilution series‚ then placed in a spectrophotometer set to 525 nm. The absorbance of the dilution was used to create a standard curve for betacyanin. Discs of living
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was separated into four stages‚ the first being preparation of cell competency. In this stage two vials were placed in ice baths‚ one vial containing 50 µL of E. coli and the other containing a CaCl2 solution. 630 µL of the CaCl2 solution was then transferred to the E. coli vial‚ using a sterile pipet. After tapping the tube to mix the solution‚ it was then returned to the ice bath to continue incubation for at least 10 minutes. The cell competency preparation was carried out by the instructor in this
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