Report subject: Serum protein electrophoresis. Report No.: 1. Serum Protein Electrophoresis (SPEP) Introduction: The serum protein electrophoresis (SPEP) test measures specific proteins in the blood to help identify some diseases. And its uses an electrical field to separate the proteins in the blood serum into groups of similar size‚ shape‚ and charge. And here we’ll use gel electrophoresis which indicate that blood serum is placed on special paper treated with agarose gel and exposed to an
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major dietary sources of each. a. Proteins b. Carbohydrates c. Fats . Janine made this statement: “… if your brain doesn’t get carbs—well‚ glucose‚ anyway—you get really cranky. You have to have enough carbs.” Find out if Janine is right. How does the nervous system use glucose? . Janine also said: “If you eat way too much protein and not enough carbs you can ruin your kidneys forever because of all the nitrogen you have to process breaking down the protein.” Find out if Janine is right about
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in the fragmentation of the DNA. Protein glycosylation may be an additional damaging factor . In the attempt to repair DNA‚ poly(ADP-ribose) polymerase (PARP) is overstimulated. This diminishes cellular NAD+‚ and subsequently ATP‚ stores the depletion of the cellular energy stores ultimately results in beta cell necrosis. Although streptozotocin also methylates proteins ‚DNA methylation is ultimately responsible for beta cell death‚ but it is likely that protein methylation contributes to the functional
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Denaturation of proteins involves the disruption and possible destruction of both the secondary and tertiary structures. Since denaturation reactions are not strong enough to break the peptide bonds‚ the primary structure (sequence of amino acids) remains the same after a denaturation process. Denaturation disrupts the normal alpha-helix and beta sheets in a protein and uncoils it into a random shape. Denaturation occurs because the bonding interactions responsible for the secondary structure (hydrogen
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The Isolation‚ purification and identification of Proteins assayed From Bovine Liver Using SDS Gel Electrophoresis‚ Mass Spectroscopy and Western Blotting Abstract The purpose of the experiment was to isolate and recognize varying protein solubilization and assaying methods by using bovine liver protein. The experiment implicated the impact of different types of solvents like ethanol‚ water‚ PBS‚ PBS+1% Triton x-100‚ and PBS+2% SDS on protein solubilization. Bradford and Ghosh/Dumbroff methods
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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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Receptor Protein Protein that binds to a specific single molecule‚ enabling the cell to respond to the signal molecule. i.e. The muscles of a person exercising can not contract without receptor proteins and signal molecules that tell the muscles when to contract and when to relax. Second Messenger Signal molecule produced in response to the binding of a chemical signal. Acts as a signal molecule in the cytoplasm. Signal Molecule Carries information throughout the body and to other
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Objectives: 1) To study and understand the steps for extract bacteria plasmid DNA. 2) To measure the concentration and purity of extracted DNA by using spectrometric method and agarose gel electrophoresis method. 3) Determine the size of extracted DNA by using agarose gel electrophoresis method. Materials and Methods: (Refer to UDEE2124 lab manual from page 7 to page 10) Results: (I) Spectrophotometric Determination of DNA A260 = 3.923
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EXPERIMENT NO. 15 PROTEIN CHARACTERIZATION BY ELECTROPHORESIS Abstract The molecular weights of protein extracts were assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). Two sets of four protein samples‚ standard bovine serum albumin (BSA)‚ invertase‚ egg albumin‚ and casein‚ were prepared; one set containing β-mercaptoethanol (BME) while the other did not. These were then analyzed through SDS-PAGE with 12.5% resolving gel‚ prepared using 2 M Tris-HCl at pH 8
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of Muscle Proteins to Infer Evolutionary Relationships of Mammals‚ Fish and Birds Abstract This experiment used electrophoresis to examine the makeup of muscle proteins from two mammals (cow‚ Bos taurus; bear‚ Ursus americanus)‚ two aves (chicken‚ Gallus gallus; turkey‚ Meleagris gallopavo)‚ and two fish (King Salmon‚ Oncorhynchus tshawytscha; Albacore Tuna‚ Scombridae unclassified). The hypothesis was that as species have diverged evolutionarily‚ the makeup of their muscle proteins has also
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