Talk:In situ hybridization

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What about:

In Situ Hybridization - the localization of specific mRNA or DNA species in tissues, cells or chromosomes using nucleic acid probes.

Nucleic acid hybridization techniques rely upon the fact that complementary sequences of single-stranded nucleic acid species spontaneously re-anneal, under appropriate conditions, to form a double-stranded hybrid (duplex). Since it is possible to incorporate isotopic or non-isotopic markers into nucleic acids, either enzymatically or photochemically, we can use these labelled nucleic acid molecules as probes to study the distribution or level of expression of specific genes or gene transcripts.


In situ hybridization, or hybridization histochemistry, was introduced in 1969 (Buongiorno-Nardelli MAW et al. Nature, 225: 946-7; John, HL et al. Nature, 223: 912-3). The basic technique uses the fact that DNA or RNA (probes) will undergo hydrogen bonding to complimentary sequences of DNA or RNA in the cells or organisms (Hybridization).With the help of these probe DNAs or RNAs, the target gene or mRNA be visulized. In Situ Hybridization can be used to view the location of nucleic acidsequences (genes) in situ (ie. in their native location in the cell or nucleus).

Assessment comment

The comment(s) below were originally left at Talk:In situ hybridization/Comments, and are posted here for posterity. Following several discussions in past years, these subpages are now deprecated. The comments may be irrelevant or outdated; if so, please feel free to remove this section.

The test is used to identify RNA sequences and not DNA sequences in a peice of tissue. That is because tyhe probe used and the target identified must be single-stranded. please correct.

Last edited at 10:32, 8 November 2006 (UTC). Substituted at 18:49, 29 April 2016 (UTC)