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Automation and basic techniques in medical microbiology / / Santi M. Mandal and Debarati Paul
Automation and basic techniques in medical microbiology / / Santi M. Mandal and Debarati Paul
Autore Mandal Santi M.
Pubbl/distr/stampa Gateway East, Singapore : , : Springer, , [2022]
Descrizione fisica 1 online resource (213 pages)
Disciplina 616.9041
Soggetto topico Medical microbiology
Microbiology - Technique
Microbiologia mèdica
Metodologia de la ciència
Soggetto genere / forma Llibres electrònics
ISBN 1-0716-2372-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intro -- Preface -- Acknowledgements -- Contents -- About the Authors -- 1: Good Laboratory Practices -- 1.1 Introduction -- 1.2 Basic Record and Lab Note Book -- 1.3 Laboratory Safety Equipment -- 1.4 Biosafety Levels and Practices -- 2: Automation in Medical Microbiology -- 2.1 Introduction -- 2.2 Applications of Automation -- 2.3 Advantages and Disadvantages -- 2.3.1 Advantages of Using Auto-analysers -- 2.3.2 Disadvantages of Automation -- 2.4 Types of Auto-analysers -- 2.5 History of Auto-analysers -- 2.6 Laboratory Automation and Total Laboratory Automation -- 2.7 Types and Applications of Auto-analysers in Microbiology -- 2.7.1 Microbiological Specimen Processor -- 2.7.2 Routine Biochemistry Analysers -- 2.7.3 Immunology-Based Analysers -- 2.7.4 Haematology Analysers -- 2.7.5 Cell Counter -- 2.7.6 Coagulometer(s) -- 2.7.7 Additional Instrument for Haematology-Based Methods -- 2.7.8 Other Miscellaneous Analysers -- References -- 3: Manual and Automated Characterization of Multi-antibiotic-Resistant (MAR) Bacteria -- 3.1 Introduction -- 3.2 Types of Antibiotic Sensitivity Tests -- 3.2.1 Kirby-Bauer Disc Diffusion Method -- 3.2.2 The Minimum Inhibitory Concentration (MIC) Method -- 3.2.3 RAPD PCR Analysis -- 3.2.4 Multiplex PCR -- 3.2.5 Padlock PCR and Microarray Analysis -- 3.2.6 Real-Time PCR for Quantitative Data -- References -- 4: Rapid Microbial Genome Sequencing Techniques and Applications -- 4.1 Introduction -- 4.2 WGS Techniques -- 4.3 Data Analysis -- Protocol for WGS (adapted from Gautam et al. 2019) -- 4.4 Applications -- 4.5 Challenges -- References -- 5: Spectroscopy: Principle, Types and Microbiological Applications -- 5.1 Introduction -- 5.2 General Types of Spectra -- 5.2.1 Continuous Spectra -- 5.2.2 Discrete Spectra -- 5.2.2.1 Emission Line Spectra -- 5.2.2.2 Absorption Line Spectra -- 5.3 Principle of Spectroscopy.
5.4 Optical Instruments in Spectroscopy -- 5.5 Is Spectroscopy Different from Spectrometry? -- 5.6 Uses of Spectroscopy -- 5.7 Types of Spectroscopy -- 5.7.1 Ultraviolet and Visible Spectroscopy -- 5.7.1.1 Background -- 5.7.1.2 Principle -- 5.7.1.3 Applications of UV-Vis Spectroscopy -- 5.7.1.3.1 Spectroscopy in Environmental Analysis -- 5.7.1.3.2 UV-Vis Spectroscopy for Water Analysis and Environmental Applications -- 5.7.1.3.3 Spectrophotometric Analysis of Bacterial Water Contaminants -- 5.7.1.3.4 Spectrophotometers for Chlorine and Flouride Quantification -- 5.7.1.3.5 UV-Vis Spectroscopy for Geological Studies Linked to Water Contamination -- 5.7.1.3.6 Other Applications -- 5.7.2 Infrared Spectroscopy -- 5.7.2.1 Introduction -- 5.7.2.1.1 Molecular Vibrations and Vibrational Frequency -- 5.7.2.1.1.1 Vibration of Diatomic Molecules -- 5.7.2.1.1.2 Vibrational Transitions -- 5.7.2.1.1.3 Types of Vibrations (Sharma 2007) -- 5.7.2.2 Instrumentation -- 5.7.2.2.1 Source -- 5.7.2.2.2 Sample Types and Preparation -- 5.7.2.2.3 Various Types of Detectors Used -- 5.7.2.3 FTIR (Fourier Transform IR Spectrometers) -- 5.7.2.4 Advantages of FTIR -- 5.7.2.5 Applications of IR Spectroscopy -- 5.7.3 Mass Spectrometry -- 5.7.3.1 The Mass Spectrometer -- 5.7.3.2 The Nature of Mass Spectra -- 5.7.3.3 The Working Principle of a Mass Spectrometer -- 5.7.3.4 Applications of Mass Spectrometry -- 5.7.3.4.1 Analysis of Biomolecules -- 5.7.3.4.2 Analysis of Glycans -- 5.7.3.4.3 Analysis of Lipids -- 5.7.3.4.4 Analysis of Proteins and Peptides -- 5.7.3.4.5 Analysis of Oligonucleotides -- 5.7.4 Nuclear Magnetic Resonance (NMR) Spectroscopy -- 5.7.4.1 NMR Spectrum -- 5.7.4.2 NMR Spectrometers -- 5.7.4.3 Applications of NMR -- 5.8 Applications of Spectroscopy in Microbiology -- References -- 6: MALDI-TOF MS for Bacterial Identification -- 6.1 Introduction.
6.2 MALDI: Sample Preparation and Analysis -- 6.2.1 Sample Preparation -- 6.2.2 Protein Digestion -- 6.2.3 MALDI/MS Analysis -- 6.3 Uses of MALDI-TOF -- 6.4 MALDI-TOF MS-Based Antimicrobial Susceptibility Testing -- 6.4.1 Detection of Antibiotic Degradation -- 6.4.2 Identification of Biomarker for Detecting Antibiotic-Resistant Strains -- 6.4.3 Phenotypic Antibiotic Resistance Analysis of Bacterial Strains -- 6.5 Advantages and Limitations -- 6.6 Challenges -- References -- 7: Enzyme-Linked Immunosorbent Assay (ELISA) -- 7.1 Introduction -- 7.2 Indirect ELISA -- 7.2.1 Steps of Indirect ELISA -- 7.3 Direct or Sandwich ELISA -- 7.3.1 Steps of Double Antibody Sandwich (DAS) ELISA -- 7.3.2 Steps of Triple Antibody Sandwich (TAS) ELISA -- 7.4 Competitive ELISA -- 7.5 Radioimmunoassay (RIA) -- 7.5.1 Steps of RIA -- 7.6 Automated ELISA -- References -- 8: Isolation of Normal Microbiota from the Human Body and Microbial Identification -- 8.1 Introduction -- 8.2 Collection of Samples from Various Parts of the Body -- 8.3 Biochemical Tests for Identification of Bacteria -- 8.3.1 Carbohydrate Fermentation -- 8.3.2 Indole Production Test -- 8.3.3 Methyl Red Test -- 8.3.4 Voges-Proskauer Test -- 8.3.5 Citrate Utilization -- 8.3.6 Urease Test -- 8.3.7 Catalase Test -- 8.3.8 Coagulase Test -- 8.3.9 Lactophenol Cotton Blue -- 8.4 Rapid Multitest Systems -- 8.4.1 Automated Validation of Every Result (VITEK) System for Microbial Identification -- 8.4.2 Biolog: Phenotype Microarrays -- 8.4.3 Electromigration Techniques -- 8.4.4 MIDI Sherlock System for FAME Analysis -- 8.5 Computer-Aided Gene Analysis for Identification of Microbes -- 8.5.1 Ribosomal RNA Gene Sequencing -- 8.5.2 Phylogenetic Analysis -- 8.5.3 Generating Multiple Sequence Alignments -- 8.6 Conclusion -- References -- 9: Microarrays and Its Application in Medical Microbiology -- 9.1 Introduction.
9.2 Basic Principle -- 9.3 Immobilization Strategies Used for Preparing Microarrays -- 9.4 Manufacture of the Different Components of Microarrays -- 9.4.1 Oligonucleotide Synthesis -- 9.5 Properties of Fluorescence and Fluorophores -- 9.6 Measuring Fluorescence -- 9.7 Labelling Samples for Analysis of Gene Expressions -- 9.8 Labelling Strategies -- 9.8.1 Labelling Bacterial Transcripts -- 9.9 Labelling Samples for Gene Expression Microarray -- 9.10 Calculating Label Density in Probe -- 9.11 Steps for Microarray Hybridization -- 9.12 Different Slide Types for Microarray -- 9.13 Comparing Automated and Manual Hybridization (Table 9.2) -- 9.14 Imaging for Microarray System -- 9.15 Optical System for Imaging in Microarray -- 9.16 Detector System, Amplifier System and Digital Resolution for Imaging in Microarray -- 9.17 Scanners and Excitation Light System for Microarray -- 9.18 Data Analysis in Microarray -- 9.19 Normalization of Data for Correcting Experimental Variation Between Slides -- 9.20 Visualizing of Data and Clustering -- 9.21 Troubleshooting During Microarray-Based Experiments -- 9.22 Applications of Microarrays -- 9.23 Limitations of Microarray Technique -- 9.24 Conclusion and Future Direction -- References -- 10: Immunotechnology -- 10.1 Introduction -- 10.1.1 Monoclonal Antibodies: Purification and Concentrate -- 10.1.1.1 Principle -- 10.1.1.2 Method -- 10.1.2 Concentrate the Purified Antibody -- 10.1.3 Analysis and Quality Assurance -- 10.1.4 Preparation of Separation Gel -- 10.1.5 Preparation of Protein Sample and Loading -- 10.1.6 Staining and Distaining of the Gel -- 10.1.7 Quality Assurance -- 10.2 Immunoelectrophoresis -- 10.2.1 Protocol -- 10.3 Western Blotting -- 10.3.1 Required Material -- 10.3.2 Protocol -- 10.3.3 Blocking of Membrane -- 10.3.4 Binding of Primary Antibody -- 10.3.5 Binding of Secondary Antibody.
10.4 Determination of Cell Number -- 10.4.1 Required Material -- 10.4.2 Method -- 10.5 Immunofluorescence Assay -- 10.5.1 Principle -- 10.5.2 Immunofluorescence Technique -- 10.5.3 Labelling of Antibodies with Fluorochromes -- 10.5.4 Detection of Fluorochrome-Labelled Reagent -- 10.5.5 Selection of Fluorochrome -- 10.5.6 Materials -- 10.5.7 Blocking Buffer -- 10.5.8 Dilution Buffer -- 10.5.9 Fixative Solution -- 10.5.10 Immunostaining -- 10.5.11 Immunofluorescence Staining Method -- 10.5.12 Uses -- References -- 11: Advances in Microscopy -- 11.1 Introduction -- 11.2 Light Microscopy -- 11.2.1 Physical Properties of Light -- 11.2.2 Reflection -- 11.2.3 Transmission -- 11.2.4 Absorption -- 11.2.5 Refraction -- 11.2.6 Diffraction -- 11.2.7 The Human Eye -- 11.2.8 Polarization -- 11.2.9 Fluorescence -- 11.2.10 Important Concepts in Microscopy -- 11.2.11 Contrast -- 11.2.12 Magnification -- 11.2.13 Sensitivity -- 11.2.14 Simple Theory of Microscopy -- 11.2.15 Metric Units Used in Microscopy -- 11.2.16 Light Microscopes -- 11.2.16.1 The Compound Light Microscope -- 11.2.16.2 Inverted Microscope -- 11.3 Dark Field Microscope -- 11.4 Phase Contrast Microscopy -- 11.5 Differential Interference Contrast Microscopy (DIC) -- 11.6 Fluorescence Microscopy -- 11.6.1 Fluorescent Antibody Technique or Immunofluorescence -- 11.6.2 Identification of Chromosome -- 11.6.2.1 Fluorescence In Situ Hybridization (FISH) -- 11.7 Polarization Microscopy -- 11.8 Confocal Microscopy -- 11.9 Electron Microscopy -- 11.9.1 Introduction -- 11.9.2 Transmission Electron Microscope (TEM) -- 11.9.3 Scanning Electron Microscope -- 11.9.4 Scanning Tunneling Microscope (STM) -- 11.9.5 Atomic Force Microscope -- 11.9.6 Sample Preparation for Light Microscope -- 11.9.6.1 Wet Mount Method -- 11.9.7 Histological Techniques -- 11.9.8 Sample Preparation for Electron Microscope.
11.9.9 Sample Preparation of TEM and SEM.
Record Nr. UNINA-9910561300603321
Mandal Santi M.  
Gateway East, Singapore : , : Springer, , [2022]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Bacterial Adaptation to Co-resistance / / edited by Santi M. Mandal, Debarati Paul
Bacterial Adaptation to Co-resistance / / edited by Santi M. Mandal, Debarati Paul
Edizione [1st ed. 2019.]
Pubbl/distr/stampa Singapore : , : Springer Singapore : , : Imprint : Springer, , 2019
Descrizione fisica 1 online resource (VII, 322 p. 50 illus., 27 illus. in color.)
Disciplina 630
Soggetto topico Ecologia microbiana
Agriculture
Microbial ecology
Molecular ecology
Biodiversity
Cell biology
Microbial Ecology
Molecular Ecology
Cell Biology
Soggetto genere / forma Llibres electrònics
ISBN 981-13-8503-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 1. Plasmids: The necessary Knowledge Wealth for Encountering Antibiotic-Resistance menace -- Chapter 2. Disinfectants amend the expression of membrane bound efflux transporters to augment antimicrobial resistance -- Chapter 3. Knowledge gaps and research needs in bacterial co-resistance in the environment -- Chapter 4. Microbial resistance to Antibiotics -- Chapter 5. Do non-medical uses of antibiotics develop cross-resistance in clinical pathogens? -- Chapter 6. Biofilms in antimicrobial activity and drug resistance -- Chapter 7. GAntimicrobial resistance in microbes: Mode of action of TolC like protein and their mechanism of regulating stress resistance and physiology -- Chapter 8. Efflux mediated co-resistance -- Chapter 9. Biofilm and Antibiotic resistance in Acinetobacter baumannii -- Chapter 10. Mechanism of bacterial co-resistance -- Chapter 11. Antibiotics and Microbial Antibiotic Resistance in Soil -- Chapter 12. Microbial adaptation and resistance to pesticides -- Chapter 13. Antimicrobial agents used in food preservation or as agricides and effect on microbes in developing antimicrobial resistance -- Chapter 14. Molecular Mechanisms of Action and Resistance of Antimalarial drugs -- Chapter 15. Management and control of antimalarial drug resistance.
Record Nr. UNINA-9910373917303321
Singapore : , : Springer Singapore : , : Imprint : Springer, , 2019
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui