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  2. Fluorescence in situ hybridization - Wikipedia

    en.wikipedia.org/wiki/Fluorescence_in_situ...

    FISH can be incorporated into Lab-on-a-chip microfluidic device. This technology is still in a developmental stage but, like other lab on a chip methods, it may lead to more portable diagnostic techniques. [28] [29] General process of fluorescent in situ hybridization (FISH) used for bacterial pathogen identification.

  3. Flow-FISH - Wikipedia

    en.wikipedia.org/wiki/Flow-FISH

    Flow-FISH (fluorescence in-situ hybridization) is a cytogenetic technique to quantify the copy number of RNA or specific repetitive elements in genomic DNA of whole cell populations via the combination of flow cytometry with cytogenetic fluorescent in situ hybridization staining protocols. [1] [2] [3]

  4. Q-FISH - Wikipedia

    en.wikipedia.org/wiki/Q-FISH

    Quantitative Fluorescent in situ hybridization (Q-FISH) is a cytogenetic technique based on the traditional FISH methodology. In Q-FISH, the technique uses labelled (Cy3 or FITC) synthetic DNA mimics called peptide nucleic acid (PNA) oligonucleotides to quantify target sequences in chromosomal DNA using fluorescent microscopy and analysis software.

  5. In situ hybridization - Wikipedia

    en.wikipedia.org/wiki/In_situ_hybridization

    In situ hybridization (ISH) is a type of hybridization that uses a labeled complementary DNA, RNA or modified nucleic acid strand (i.e., a probe) to localize a specific DNA or RNA sequence in a portion or section of tissue or if the tissue is small enough (e.g., plant seeds, Drosophila embryos), in the entire tissue (whole mount ISH), in cells ...

  6. Cytogenetics - Wikipedia

    en.wikipedia.org/wiki/Cytogenetics

    While radioisotope-labeled probes had been hybridized with DNA since 1969, movement was now made in using fluorescent-labeled probes. Hybridizing them to chromosomal preparations using existing techniques came to be known as fluorescence in situ hybridization (FISH). [22]

  7. Peter M. Lansdorp - Wikipedia

    en.wikipedia.org/wiki/Peter_M._Lansdorp

    During a sabbatical in Leiden University in 1995, Lansdorp developed a novel fluorescent in situ hybridization (FISH) method to measure the length of telomere repeats using novel peptide nucleic acid probes [13] - a method which has since enabled numerous studies and observations in the telomere field.