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in situ hybridization |
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hybridization /hy·brid·iza·tion/ (hi″brid-ĭ-za´shun) 1. crossbreeding; the act or process of producing hybrids. 3. formation of a heterokaryon by fusion of two somatic cells, usually of different species. 4. in chemistry, a procedure whereby orbitals of intermediate energy and desired directional character are constructed. in situ hybridization molecular hybridization used to analyze prepared cells or histologic sections in situ in order to analyze the intracellular or intrachromosomal distribution, transcription, or other characteristics of specific nucleic acids. molecular hybridization formation of a partially or wholly complementary nucleic acid duplex by association of single strands, in order to detect and isolate specific sequences, measure homology, or define other characteristics of one or both strands. in situ [L.] in its normal place; confined to the site of origin. in situ hybridization see in situ hybridization of nucleic acid. in situ hybridization A method for localizing a sequence of DNA, mRNA, or protein in a cell or tissue; the use of a DNA or RNA probe to detect a cDNA sequence in chromosome spreads or in interphase nuclei or an RNA sequence of cloned
bacterial or cultured eukaryotic cells; ISH is used to map gene sequences to chromosomal sites and detect gene expression. See cDNA, Chromosome, CISH–Chromogenic in situ hybridization, DNA sequence, Eukaryote, FISH–Fluorescent in situ
hybridization, GISH–Genomic in situ hybridization, Gene expression, Gene mapping, Hybridization, Immunoblotting, Interphase, Probe. Cf Southern blot. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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New models include chemically resistant ceramic top stirrer hotplates, which are available in two large sizes, and sophisticated metal top digital models with excellent temperature control for applications such as in-situ hybridisation, microarraying, and the fixing of microscope slides. Donor age and the frequency of disomy for chromosomes 1,13,21 and structural abnormalities in human spermatozoa using multicolour fluorescence in-situ hybridisation. With regard to technology, hybridisation techniques tend to be the major technologies utilised in the field of pharmacogenomics, and fluorescence in-situ hybridisation (FISH) continues to be widely used due to its ability to detect a variety of chromosomal and genetic aberrations such as molecular translocation deletions specific to each entity of haematological malignancies in a single non-dividing interphase cell. |
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