Fluorescence in situ Hybridization (FISH)

Protocols and Applications

Häftad, Engelska, 2016

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Fluorescence in situ Hybridization (FISH) belongs to that special category of well-established molecular biology techniques that, since their inception a few decades ago, have succeeded in keeping a prominent position within the constantly expanding list of laboratory pro- dures for biomedical research and clinical diagnostics.

Produktinformation

Utgivningsdatum2016-08-23
Mått178 x 254 x 26 mm
Vikt873 g
FormatHäftad
SpråkEngelska
SerieMethods in Molecular Biology
Antal sidor451
FörlagHumana Press Inc.
ISBN9781493957248

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Medicinsk genetik inom Medicin
Biovetenskap inom Naturvetenskap och teknik
Biokemi inom Naturvetenskap och teknik

Core Techniques.- Fluorescence in situ Hybridization (FISH), Basic Principles and Methodology.- Fluorescence In Situ Hybridization on DNA Halo Preparations and Extended Chromatin Fibres.- Detection of Nascent RNA Transcripts by Fluorescence In Situ Hybridization.- Fluorescence In Situ Hybridization Analysis of Formalin Fixed Paraffin Embedded Tissues, Including Tissue Microarrays.- Fluorescence in situ Hybridization (FISH) on Tissue Cryosections.- Multiplex Fluorescence in situ Hybridization (M-FISH).- Optical Mapping of Protein–DNA Complexes on Chromatin Fibers.- 3D-FISH on Cultured Cells Combined with Immunostaining.- Technical Advancements and Novel Adaptations.- The Comet-FISH Assay for the Analysis of DNA Damage and Repair.- Direct In Situ Hybridization with Oligonucleotide Functionalized Quantum Dot Probes.- LNA-FISH for Detection of MicroRNAs in Frozen Sections.- Chromosome Orientation Fluorescence In Situ Hybridization or Strand-Specific FISH.- Combinatorial Oligo FISH: Directed Labeling of Specific Genome Domains in Differentially Fixed Cell Material and Live Cells.- Simultaneous Visualization of FISH Signals and Bromo-deoxyuridine Incorporation by Formamide-Free DNA Denaturation.- CryoFISH: Fluorescence In Situ Hybridization on Ultrathin Cryosections.- Characterization of Chromosomal Rearrangements Using Multicolor-Banding (MCB/m-band).- Visualizing Nucleic Acids in Living Cells by Fluorescence In Vivo Hybridization.- Translational FISH: Applications for Human Genetics and Medicine.- Quality Control in FISH as Part of a Laboratory’s Quality Management System.- FlashFISH: “Same Day” Prenatal Diagnosis of Common Chromosomal Aneuploidies.- FISH for Pre-implantation Genetic Diagnosis.- PNA–FISH on Human Sperm.- POD-FISH: A New Technique for ParentalOrigin Determination Based on Copy Number Variation Polymorphism.- Sequence-Based High Resolution Chromosomal Comparative Genomic Hybridization (CGH).- ImmunoFISH on Isolated Nuclei from Paraffin-Embedded Biopsy Material.- Fluorescence In Situ Hybridization on 3D Cultures of Tumor Cells.- Simultaneous Ultrasensitive Subpopulation Staining/Hybridization In Situ (SUSHI) in HIV-1 Disease Monitoring.- Protocols for Model Organisms.- Detection of Prokaryotic Cells with Fluorescence In Situ Hybridization.- FISH as a Tool to Investigate Chromosome Behavior in Budding Yeast.- FISH on Chromosomes Derived from the Snail Model Organism Biomphalaria glabrata.- Fluorescence in situ Hybridization with Bacterial Artificial Chromosomes (BACs) to Mitotic Heterochromatin of Drosophila.- Three-Dimensional Fluorescence In Situ Hybridization in Mouse Embryos Using Repetitive Probe Sequences.- Fluorescence in situ Hybridization (FISH) for Genomic Investigations in Rat.- Fluorescence In Situ Hybridization on Early Porcine Embryos.- FISH on 3D Preserved Bovine and Murine Preimplantation Embryos.

From the reviews:“Fluorescence in situ hybridization (FISH) has been widely adopted to enable the study of uncultured target cells. This book shows many more applications in cytology. Relatively few chapters are devoted directly to microbiological applications; the strong theme of the book describes methods targeting chromosomes. … Protocols on 3-D FISH may have useful material for microbiologists, e.g. studies on biofilms. … I would suggest this is for microbiological libraries … .” (Jonathan Porter, Microbiology Today, November, 2011)