FISH article
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multicolor FISH assay for detection of chromosomal abnormalities in sperm cells
Centromere-FISH
42-color M-FISH variant that allows the detection of chromosomal abnormalities in the p- and q-arms of all 24 human chromosomes, except the p-arm of the Y and acrocentric chromosomes
armFISH
very useful for detection, identification, and quantification of microorganisms involved in bioleaching processes
Catalyzed Reporter Deposition-FISH (CARD-FISH)
used to determine the interactions of neuronal populations associated with different behaviors
Cellular Compartment Analysis of Temporal (Cat) Activity by Fish (catFISH)
involves hybridization on binucleated cells in which cytokinesis has been blocked by treatment with cytochalasin B (CB)
Cytochalasin B (CB-FISH)
allows to determine the relative orientation of two or more DNA sequences along a chromosome; useful in assessing chromosomal translocations and inversions
Chromosome Orientation (CO)-FISH
enables recognition of all human chromosome arms on the basis of color and mapping of gene and viral integration site in the context of chromosome arm painting
Combined Binary Ratio (COBRA)-FISH
This protocol is similar to CO-FISH except for the information about the directional organization of telomeric sequences.
Chromosome Orientation and Direction (COD)-FISH
used for specific labeling of genomic sites. It takes advantage of homopurine/homopyrimidine oligonucleotides that form triple helices with intact duplex genomic DNA.
Combinatorial Oligonucleotide (COMBO)-FISH
combination of comet assay and FISH analysis. It is used to detect genome region-specific DNA damage. successfully used to determine the sensitivity of telomeres to damage.
Comet-FISH
makes use of ultrathin cryosections (150 nm thick) of sucrose-embedded cells. The spatial interrelationship of chromosome territories and the genome organization in the cell nucleus has been successfully studied with this technique.
Cryo-FISH
In this FISH, a secondary color is observed since the adjacent colors overlap.
Double Fusion FISH (D-FISH)
used to determine DNA fragmentation levels in sperms
DNA Breakage Detection FISH (DBD-FISH)
BLAST-based FISH simulation program, which can predict the out- come of hybridization experiments
e-FISH
a technique in which DNA fibers or chromatin fibers are released from cell nuclei by salt or solvent extraction and stretched on a microscope slide prior to hybridization
Fiber-FISH
in situ hybridization is combined with flow cytometry for measurement of the telomeric signals from cells in suspension
Flow-FISH
initially used for identification of the 9;22 Philadelphia translocation in peripheral blood and bone marrow cells of CML patients to detect minimal residual disease after bone marrow transplantation
Fusion-Signal FISH
the cells are first permeabilized and then extracted with high salt to remove soluble protein
Halo-FISH
a method for cell cycle-controlled chromosome analysis in human lymphocytes that allows a precise quantification of induced chromosome damage for human biodosimetry
Harlequin-FISH
a combination of standard FISH and indirect or direct immuno- fluorescence. With this technique, the antigens can be visualized within the sample.
Immuno-FISH
more useful for the detection of mRNA and genes on the chromosomes
Locked Nucleic Acids (LNAs)-FISH
the ability to identify several regions or genes simultaneously using different colors; used to analyze specific chromosomal subregions, like centromeres and sub-centromeres
Multiplex (M)-FISH
refers to the simultaneous use of multiple probes in multicolor FISH. This FISH assay was initially designed to screen for multiple microdeletion syndromes in patients with unexplained developmental delay and/or mental retardation.
Multilocus or ML-FISH
first used to measure individual telomere lengths on metaphase chromosomes
Peptide Nucleic ACid (PNA)-FISH