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pubmed-article:1582257pubmed:abstractTextA double-labeling approach was applied to nonisotopic in situ hybridization with individual cosmid and plasmid clones, using digoxigenin or biotin as label and a combination of two separate enzymatic labeling methods. Probe labeling was achieved by nick translation, followed by tailing of the probe by terminal deoxynucleotidyl transferase. The double-labeling method, in conjunction with an improved detection protocol, provides for a higher signal intensity than that obtainable with single-labeled probes.lld:pubmed
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pubmed-article:1582257pubmed:articleTitleChromosomal in situ hybridization with double-labeled DNA: signal amplification at the probe level.lld:pubmed
pubmed-article:1582257pubmed:affiliationDivision of Human Biology and Human Genetics, University of Kaiserslautern, FRG.lld:pubmed
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pubmed-article:1582257pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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