Principles and Techniques of Biochemistry and Molecular Biology 7th Edition
- نویسنده(ها): Biswanath Dinda
- ویرایش: 7
- سال انتشار: 2010
- تعداد صفحات: 761 صفحه
- تعداد فصل ها: 18 فصل
- فرمت فایل: PDF رنگی
- حجم فایل فشرده: 8.01 مگابایت
99,000 تومان
Principles and Techniques of Biochemistry and Molecular Biology 7th Edition
کتاب اصول و تکنیک های بیوشیمی و بیولوژی مولکولی ویرایش 7 هفتم Principles and Techniques of Biochemistry and Molecular Biology 7th Edition یکی از کتاب های مرجع ارزشمند بیوشیمی و زیست شناسی مولکولی برای دانشجویان علوم پزشکی و بیوشیمی که توسط دو تن از اساتید شیمی Keith Wilson , John Walker واکر ویلسون تالیف و نوشته شده است. این کتاب بهترین و پرفروش ترین کتاب در مقطع کارشناسی می باشد مقدمه ای بر تکنیک های کلیدی تجربی از سراسر علوم زیست شناسی و شیمی است. منحصر به فرد تئوری ها و شیوه هایی را که رشته های زیست شناسی و پزشکی را در اختیار دارند، تطبیق می دهد و به طور جامع بیوشیمی و زیست شناسی مولکولی پوشش می دهد. این نسخه، مطالعات موردی، نشان دهنده ارتباط اصول و تکنیک های تشخیص و درمان بیماران فردی است. پوشش شامل بخش هایی در مورد سلول های بنیادی، فصل های مربوط به تکنیک های ایمنی شناختی و تکنیک های طیف سنجی و فصل های اضافی در مورد کشف و توسعه دارو و بیوشیمی بالینی است.
دانلود کتاب اصول و تکنیک های بیوشیمی و بیولوژی مولکولی واکر ویلسون ویرایش 7 هفتم به دانشجویان پزشکی و بیوشیمی به عنوان مرجعی ارزشمند پیشنهاد می شود.
مشخصات کتاب:
Principles and Techniques of Biochemistry and Molecular Biology 7th Edition
فهرست مطالب و عناوین فصل های کتاب
1 Basic principles 1
K. WILSON
1.1 Biochemical and molecular biology studies 1
1.2 Units of measurement 3
1.3 Weak electrolytes 6
1.4 Quantitative biochemical measurements 16
1.5 Safety in the laboratory 35
1.6 Suggestions for further reading
2 Cell culture techniques 38
A. R. BAYDOUN
2.1 Introduction 38
2.2 The cell culture laboratory and equipment 39
2.3 Safety considerations in cell culture 43
2.4 Aseptic techniques and good cell culture practice 44
2.5 Types of animal cell, characteristics and maintenance in culture 49
2.6 Stem cell culture 61
2.7 Bacterial cell culture 68
2.8 Potential use of cell cultures 71
2.9 Suggestions for further reading
3 Centrifugation 73
K. OHLENDIECK
3.1 Introduction 73
3.2 Basic principles of sedimentation 74
3.3 Types, care and safety aspects of centrifuges 79
3.4 Preparative centrifugation 86
3.5 Analytical centrifugation 95
3.6 Suggestions for further reading
4 Microscopy 100
S. W. PADDOCK
4.1 Introduction 100
4.2 The light microscope 103
4.3 Optical sectioning 116
4.4 Imaging living cells and tissues 123
4.5 Measuring cellular dynamics 126
4.6 The electron microscope (EM) 129
4.7 Image archiving 133
4.8 Suggestions for further reading
5 Molecular biology, bioinformatics and basic techniques 138
R. RAPLEY
5.1 Introduction 138
5.2 Structure of nucleic acids 139
5.3 Genes and genome complexity 145
5.4 Location and packaging of nucleic acids 149
5.5 Functions of nucleic acids 152
5.6 The manipulation of nucleic acids – basic tools and techniques 162
5.7 Isolation and separation of nucleic acids 164
5.8 Molecular biology and bioinformatics 170
5.9 Molecular analysis of nucleic acid sequences 171
5.10 The polymerase chain reaction (PCR) 178
5.11 Nucleotide sequencing of DNA 187
5.12 Suggestions for further reading
6 Recombinant DNA and genetic analysis 195
R. RAPLEY
6.1 Introduction 195
6.2 Constructing gene libraries 196
6.3 Cloning vectors 206
6.4 Hybridisation and gene probes 223
6.5 Screening gene libraries 225
6.6 Applications of gene cloning 229
6.7 Expression of foreign genes 234
6.8 Analysing genes and gene expression 240
6.9 Analysing whole genomes 254
6.10 Pharmacogenomics 259
6.11 Molecular biotechnology and applications 260
6.12 Suggestions for further reading
7 Immunochemical techniques 263
R. BURNS
7.1 Introduction 263
7.2 Making antibodies 273
vi Contents7.3 Immunoassay formats 283
7.4 Immuno microscopy 291
7.5 Lateral flow devices 291
7.6 Epitope mapping 292
7.7 Immunoblotting 293
7.8 Fluorescent activated cell sorting (FACS) 293
7.9 Cell and tissue staining techniques 294
7.10 Immunocapture polymerase chain reaction (PCR) 295
7.11 Immunoaffinity chromatography (IAC) 295
7.12 Antibody-based biosensors 296
7.13 Therapeutic antibodies 297
7.14 The future uses of antibody technology 299
7.15 Suggestions for further reading 299
8 Protein structure, purification, characterisation
and function analysis 300
J. WALKER
8.1 Ionic properties of amino acids and proteins 300
8.2 Protein structure 304
8.3 Protein purification 307
8.4 Protein structure determination 328
8.5 Proteomics and protein function 340
8.6 Suggestions for further reading 351
9 Mass spectrometric techniques 352
A. AITKEN
9.1 Introduction 352
9.2 Ionisation 354
9.3 Mass analysers 359
9.4 Detectors 377
9.5 Structural information by tandem mass spectrometry 379
9.6 Analysing protein complexes 390
9.7 Computing and database analysis 394
9.8 Suggestions for further reading 397
10 Electrophoretic techniques 399
J. WALKER
10.1 General principles 399
10.2 Support media 403
10.3 Electrophoresis of proteins 407
10.4 Electrophoresis of nucleic acids 422
10.5 Capillary electrophoresis 427
10.6 Microchip electrophoresis 431
10.7 Suggestions for further reading 432
11 Chromatographic techniques 433
K. WILSON
11.1 Principles of chromatography 433
11.2 Chromatographic performance parameters 435
11.3 High-performance liquid chromatography 446
11.4 Adsorption chromatography 453
11.5 Partition chromatography 455
11.6 Ion-exchange chromatography 459
11.7 Molecular (size) exclusion chromatography 462
11.8 Affinity chromatography 465
11.9 Gas chromatography 470
11.10 Suggestions for further reading 476
12 Spectroscopic techniques: I Spectrophotometric techniques 477
A. HOFMANN
12.1 Introduction 477
12.2 Ultraviolet and visible light spectroscopy 482
12.3 Fluorescence spectroscopy 493
12.4 Luminometry 507
12.5 Circular dichroism spectroscopy 509
12.6 Light scattering 514
12.7 Atomic spectroscopy 516
12.8 Suggestions for further reading 519
13 Spectroscopic techniques: II Structure and interactions 522
A. HOFMANN
13.1 Introduction 522
13.2 Infrared and Raman spectroscopy 523
13.3 Surface plasmon resonance 527
13.4 Electron paramagnetic resonance 530
13.5 Nuclear magnetic resonance 536
13.6 X-ray diffraction 546
13.7 Small-angle scattering 549
13.8 Suggestions for further reading 551
14 Radioisotope techniques 553
R. J. SLATER
14.1 Why use a radioisotope? 553
14.2 The nature of radioactivity 554
14.3 Detection and measurement of radioactivity 561
14.4 Other practical aspects of counting of radioactivity and analysis of data 573
14.5 Safety aspects 577
14.6 Suggestions for further reading
15 Enzymes 581
K. WILSON
15.1 Characteristics and nomenclature 581
15.2 Enzyme steady-state kinetics 584
15.3 Analytical methods for the study of enzyme reactions 602
15.4 Enzyme active sites and catalytic mechanisms 611
15.5 Control of enzyme activity 615
15.6 Suggestions for further reading 624
16 Principles of clinical biochemistry 625
J. FYFFE AND K. WILSON
16.1 Principles of clinical biochemical analysis 625
16.2 Clinical measurements and quality control 629
16.3 Examples of biochemical aids to clinical diagnosis 640
16.4 Suggestions for further reading 658
16.5 Acknowledgements 659
17 Cell membrane receptors and cell signalling 660
K. WILSON
17.1 Receptors for cell signalling 660
17.2 Quantitative aspects of receptor–ligand binding 663
17.3 Ligand-binding and cell-signalling studies 680
17.4 Mechanisms of signal transduction 685
17.5 Receptor trafficking 703
17.6 Suggestions for further reading 707
18 Drug discovery and development 709
K. WILSON
18.1 Human disease and drug therapy 709
18.2 Drug discovery 718
18.3 Drug development 727
18.4 Suggestions for further reading
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