1. Aminoalkylsilane-treated glass slides as support for in situ hybridization of keratin cDNAs to frozen tissue sections under varying fixation and pretreatment conditions;Rentrop, M.; Knapp, B.; Winter, H.; Schweizer, J.;Histochem J; or non-radioactive products. To use radioactive probes, in situ hybridisation must be performed in a laboratory specifically equipped to use radioactive products, and care must be,1986
2. Detection of viral genomes in cultured cells and paraffin-embedded tissue sections using biotin-labeled Virology;Brigati, D.J.; Myerson, D.; Leary, J.J.,1983
3. In situ localization of mRNA using thymine-thymine dimerized Thus non-radioactive probes are preferable for routine use in the pathology laboratory. Several non-radioactive labelling and detection methods, such as the biotin7 or sulphon8 labelling methods and the T-T dimer method,9 have been introduced. It has been pointed out, however, that these methods fall short of the radioactive method in terms of sensitivity, specificity, or convenience of labelling and detection. The DIG-ELISA system, a new DNA labelling and detection method developed by Boehringer Mannheim, has been cDNA;Nakane, P.K.; Moriuchi, T.; Koji, T.; Tanno, M.; Abe, K.;Acta Histochem Heiles HBJ, Genersch E, Cytochem,1987
4. DNA fingerprinting using non-radioactive oligonucleotide probes specific for simple repeats;Schafer, R.; Zischler, H.; Epplen, J.T.;Nucleic Acids Res; Herrington CS, McGee JO'D,1988