University of Oxford Computing Laboratory MSc Computer Science Dissertation Automatic Generation of Control Flow Hijacking Exploits for Software Vulnerabilities Author: Sean Heelan Supervisor: Dr. Daniel Kroening September 3‚ 2009 Contents List of Figures v List of Tables vii List of Code Listings ix Acknowledgements xi Abstract 1 1 Introduction 3 1.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 1.2 Motivation . . .
Premium Central processing unit
Procedure: Day 1: Buffer preparation First‚ the buffer was prepared by using the formula as follows: Figure 1: Calculation for prepare 0.5 M Tris buffer at pH 6.8 3.033 g of Tris was weighed and placed in 400 mL beaker. Then‚ 25 mL of distilled water was added into the beaker that contained Tris. The mixture was dissolved using the stirring rod‚ and then the magnetic stirring bar was placed in the beaker for further dissolve when measuring the pH. The pH meter was used to measure the solution
Premium Chemistry Water Chemical reaction
to measure the absorbance of catecholase in solutions with different concentrations of potato juice and phosphate buffers. Absorbance of the enzyme catecholase was at an optimum level when pH was close to neutral. When pH was acidic or basic‚ the catecholase was less effective. Also‚ when there was a higher concentration of potato juice and a lower concentration of phosphate buffer‚ absorbance of the enzyme increased. Introduction According to Edmund J. Stellwag‚ in his article "Enzyme" an
Premium PH Buffer solution Enzyme
of pH on invertase activity is the primary objective of the experiment. Dinitrosalicyclic acid (DNS) Assay method is utilized to monitor the enzymatic activity of invertase. Invertase was subjected to different pH (3.87‚ 4.0‚ 5.5‚ 7.3 and 10.55) of buffer solution and was observed under 540 nm absorbance using spectrophotometer. After observation and analysis‚ a peak (optimum pH) was observed by plotting absorbance versus pH. INTRODUCTION Enzymes are proteinaceous catalysts‚ which speed up the
Free PH Buffer solution Enzyme
at a carbon fiber microdisk electrode(CFE) was developed for the determination of nicotine. Effects of detection potential‚ concentration and pH value of the phosphate buffer‚ and injection time as well as separation voltage were investigated. Under the optimized conditions: a detection potential of 1.20 V‚ 40 mmol/L phosphate buffer(pH 2.0)‚ a sample injection time of 10 s at 10 kV and a separation voltage of 16 kV‚ the linear range obtained was from 5.0×10–7 mol/L to 1.0×10–4 mol/L with a correlation
Premium Buffer solution Tobacco PH
the appropriate buffer solution to each. ( I will be testing pH 4‚5‚7‚8‚8.8 and 10) 3. Add 4cm³ of distilled water and 4cm³ of the appropriate buffer solution to 6 control test tubes labelled CA-CF to see if the pH alone will affect anything. 4. Place all test tubes in a water bath (40-45oC) and put the 1cm x 1cm squares of film in to them and start the stop clock. 5. From time to time‚ check if the squares have cleared and note down the times. 6. Repeat 3 times. Results pH buffer Actual pH Time for
Premium Enzyme PH Buffer solution
OBJECTIVE: The experiment was carried out to investigate the effects of the increase in the enzyme concentration on the rate of reaction. By using self investigative and experimental skills‚ the experiment was done in order to determine how the rate of reaction will be altered‚ whether it will increase‚ decrease or remain constant when the different concentration of enzymes added. INTRODUCTION: Enzymes are produced naturally in plant‚ animal‚ and microbial cell. There are thousands of different
Premium PH Oxygen Buffer solution
[Accessed 22 Oct. 2014]. Inkling.com‚ (2014). Inkling. [online] Available at: https://www.inkling.com/read/marks-medical-biochemistry-lieberman-marks-4th/chapter-45/i--plasma-proteins-maintain [Accessed 13 Oct. 2014]. Media.lanecc.edu‚ (2014). Chemical Buffer Systems and Acid-Base Balance. [online] Available at: http://media.lanecc.edu/users/driscolln/RT127/Softchalk/Acid_Base_Lesson/Acid_Base_Lesson4.html [Accessed 13 Oct. 2014]. Research.vet.upenn.edu‚ (2014). Milk Urea Nitrogen. [online] Available at:
Premium PH Buffer solution Blood
Abstract A buffer is a solution that resists changes in pH when H+‚ OH-‚ or H20 is added. By using standard lab equipment‚ a lab pro diagnostic tool‚ and acidic and basic solutions‚ the pH can be found. By recording the pH while adding a base or an acid gradually to a buffer solution you can find the capacity of each buffer to resist drastic changes in pH. The best buffers will keep a solution from becoming either too acidic or basic with the addition of a strong base or acid. Introduction The
Premium Acid dissociation constant Sodium hydroxide PH
determine technique accuracy in calculating the actual concentration of an acetaminophen elixir. Five standard solutions of acetaminophen and an acid buffer solution were created and analyzed with a potentiostat to determine the peak anodic voltage and current during the scanning process. Three solutions of Tylenol®—containing acetaminophen—and acid buffer were then created and scanned at the same scan rate as the five standard solutions. Additionally‚ the most concentrated standard solution was scanned
Premium Buffer solution Electrochemistry Arithmetic mean