Protein synthesis is one of the most fundamental biological processes. To start off‚ a protein is made in a ribosome. There are many cellular mechanisms involved with protein synthesis. Before the process of protein synthesis can be described‚ a person must know what proteins are made out of. There are four basic levels of protein organization. The first is primary structure‚ followed by secondary structure‚ then tertiary structure‚ and the last level is quaternary structure. Once someone understands
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Lipid Panels Case Study Subject #1 This fifty year old man that has no apparent health problems has a low ‘HDL’ of 30mg/dl. That’s not a good thing because he’ll be more likely to develop heart disease or have a heart attack/stroke. Anything over 60mg/dl is considered to be optimal. He is border line high for LDL’s of 160mg/dl‚ the ideal number is 100mg/dl or lower. That number tells me he is at greater risk to heart disease and/or heart attack. Better diet and exercise would help him tremendously
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and the quantification of albumin and casein were performed and analyzed after extraction of the said proteins from their respective sources. Isolation of proteins was initiated by the breakage of the cell wall / membranes in three different ways. Homogenization of invertase‚ albumin and casein were achieved via grinding process‚ addition of 1M acetic acid and acidification by 0.1M hydrochloric acid correspondingly. Extraction of invertase and casein involved precipitation through the utilization of
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Protein Misfolding Brittany Mascarenhas (ID: 20471654) Corey Nixon Biol 130 Tuesday October 23‚ 2012 In an organism‚ almost every dynamic function relies on proteins. A protein ’s function is a direct result of their intricate folding‚ the simplest level of which is the sequence of amino acids. (Fitzpatrick et al‚ 2011). Each amino acid has a unique characteristic because of the physical and chemical properties in their side chains‚ which affects the function of a protein
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DENATURATION OF PROTEINS Abstract The experiment was done to be able to understand how various denaturants such as HCl and NaOH affects proteins. It was observed that different denaturants act upon or denature protein differently. This was determined using the principle of viscometry. An Ostwald viscometer was used to measure the viscosity of the prepared native‚ blank‚ denatured native and blank with denaturant solutions. The time required for the said solutions to pass through the viscometer
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Abstract This experiment aimed to study the effect of various denaturants on albumin and casein protein extracts through viscosity measurements. 5 mL samples of native and denatured protein solutions were prepared‚ using -mercaptoethanol‚ urea and SDS as denaturants for albumin‚ and NaOH‚ NaCL‚ HCL‚ -mercaptoethanol‚ urea and SDS for casein. 5 mL blank solutions for each denaturant used were also prepared. The viscosity of the solutions were determined using Ostwald viscometer. ________
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Characterization of Proteins‚ aims to isolate casein from milk and albumin from egg; to explain the methods employed for protein extraction; to apply spectrophotometric methods in characterizing and quantifying extracted casein and albumin. The experiment was divided into 2 parts; the extraction of Albumin from egg and the determination of protein concentration via the Warburg-Christian method and Bradford Assay method. In the first part‚ egg white underwent the addition of a weak acid‚ disruption of
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substitutes; fats; free foods; combination foods; fast foods; and alcohol. Carbohydrate Counting When you eat a healthy meal or snack‚ it is usually a mixture of carbohydrate‚ pro- tein‚ and fat. However‚ your body changes carbohydrate into glucose faster than it changes protein and fat into glucose. It is the carbohydrate that makes your blood glucose level go up. In carbohydrate counting‚ you count foods that are mostly carbohydrate. These include starches (breads‚ cereals‚ pasta)‚ fruits and fruit
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BIOL 1F90 Expt. #1: Protein Quantification Student Name: Carlos Osorio Student ID: 5220710 Lab Section: 34 Date Experiment Performed: Sept. 26th‚ 2012 Lab Partners: K. Cloutier J. Yang ABSTRACT Protein concentration analysis is primarily done through an accepted form commonly referred to as the Bradford Protein Assay. The main purpose of this experiment was to observe and record the various protein samples’ absorbency values through the calibrated readings of a spectrophotometer
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living creatures‚ work together in a certain process that is crucial to existence: the formation of proteins. Although all species differ from each other in various ways‚ the processes by which proteins are synthesized are the same in all. Protein synthesis is a very complex process. In order to understand the process‚ there some basics that are essential for cells to create the proper proteins. DNA is a very long and double-stranded molecule that contains coding‚ through four nitrogen bases (adenine
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