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BIOCHEMISTRY EXPERIMENT SSheng Zhao ( 赵晟 ) WWeb for lecture slides : http://teaching.ewindup.info EEmail/QQ /MSN/gchat: shengzhao@seu.edu.cn or windupzs@gmail.com MMobile:18551669724 or 13675130010 Principle + Practice Logic analysis
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Introduction From public criticism: some schools teach current students by past knowledge to face the future world. How to face the future ?: deal with the real world. How to deal with the real world? Data and facts Professor John Ross: fighting with rumors using the data and facts on Sina Weibo, the Chinese Twitter. As foreign students: conduct ex periments carefully and no cheat on exam. Principle + practicelogic analysis
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Introduction Biochemistry: Biology Chemistry Molecular level Biologic structures and functions. Major methods: Laboratory assays Interdisciplinary
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Examination for Biochemistry class 1.Class participation: 20% Lecture and experimental training, logic analysis, and experiment reports. 2.Experiential exam: 10% Perform a specified experiment independently. 3.Exam on biochemistry theory (Lecture): 70%
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Preview. Wear the white coat. Be on time. Reagents back to place after usage. Welcome for any question. Finish report in class. Clean the room after class. Requirement
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1.Title; 2.Principle ; 3.Procedures(simple) ; 4.Results and analysis; 5.Conclusions. Report (Weibo/Twitter style)
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Using the pipette
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Adjustable : 0.5-2ΜL, 2-20ΜL, 20-200ΜL, 100-1000ΜL, 1000- 5000ΜL
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Usage : 1.Select the right pipette and tips 2.Holding of pipette 3.Sampling 4.expelling of liquid 5.Discharge the pipette tip
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Class syllabus by logic Protein quantification: Folin phenol (Lowry) assay Ion exchange chromatography for the mixed amino acids Transamination Protein purification Gel filtration chromatography Sodium dodecyl sulfate-Polyacrylamide gel electrophoresis (SDS-PAGE) Serum triglyceride (TG) measurement Plasmid DNA extraction, restriction enzyme digestion, and agarose gel electrophoresis Enzyme Km Serum glutamic-pyruvic transaminase (ALT) measurement (Exam!) Protein analysis Nucleic acid analysis Protein function Lipid analysis
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Class syllabus by real experiments 1.Introduction and Protein quantification: Folin phenol (Lowry) assay 2.Protein purification: Gel filtration chromatography 3.Plasmid DNA extraction, restriction enzyme digestion, and agarose gel electrophoresis 4.Enzyme Km 5.Transamination 6.Sodium dodecyl sulfate-Polyacrylamide gel electrophoresis (SDS- PAGE) 7.Ion exchange chromatography for the mixed amino acids 8.Serum triglyceride (TG) measurement 9.Serum glutamic-pyruvic transaminase (ALT) measurement (Exam!)
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PROTEIN QUANTIFICATION: FOLIN PHENOL (LOWRY) METHOD Folin phenol (Lowry) assay Usage of spectrophotometer Plotting of standard curve
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Common methods for protein quantification 1.UV Spectrophotometry 2.Lowry assay 3.Coomassie brilliant blue -G250
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Folin phenol (Lowry) assay Step 1 Under alkaline condition protein reacts with Cu and forms complex Dark blue A 650 In a certain range the strength of the color is proportional to protein concentration. Complex reduce the phenol reagents Step 2
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Spectrophotometry Lambert―Beer law : In optics, the Lambert―Beer law relates the absorption of light to the properties of the material through which the light is travelling.
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Advantage Simple and sensitive (25-250 μg) Disadvantage Time consuming , interfered by a wide variety of chemicals Sensitivity: 5 µ g/ml , Measurement range: 25~250 µg/ml
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1.Use the standard solution. 2.Measure the absorption at a certain wave length. 3.Plot the standard curve: absorbance as ordinate and the protein as horizontal coordinate. Standard curve
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Cross the zero point A is between 0.05 ~ 1.0 650nm 0.125 0.25 0.375 0.5 0.625 mg
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Procedure ( 7 tubes ) 1234567 Standard solution —0.20.40.60.81.0— Measured sample ——————1.0 H2O1.00.80.60.40.2—— A5555555 Mixing, 10min at RT B0.5 Mixing, 30min, 650nm Absorption Protein content (μg) A 650nm
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REPORT Title Principle Procedure Results and analysis tube1234567 A Standard curve
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