초록 ▼

To preserve RNA in a biological sample for analysis, the sample is incubated with an RNA preservative capable of precipitating RNA in an aqueous solution, such as a triphenylmethane dye (e.g., methyl green, crystal violet, pararosaniline, or tris-(4-aminophenyl)methane), cresyl violet, or cobalt ion

To preserve RNA in a biological sample for analysis, the sample is incubated with an RNA preservative capable of precipitating RNA in an aqueous solution, such as a triphenylmethane dye (e.g., methyl green, crystal violet, pararosaniline, or tris-(4-aminophenyl)methane), cresyl violet, or cobalt ions. RNA preservation may be used in an immunostaining assay and other histochemical methods.

대표청구항 ▼

What is claimed is: 1. A method of analyzing a biological sample comprising: precipitating RNA in the biological sample by incubating the biological sample with an RNA preservative in an aqueous solution to yield a biological sample containing preserved RNA; histochemically staining the biological

What is claimed is: 1. A method of analyzing a biological sample comprising: precipitating RNA in the biological sample by incubating the biological sample with an RNA preservative in an aqueous solution to yield a biological sample containing preserved RNA; histochemically staining the biological sample containing preserved RNA; histochemically analyzing the stained biological sample containing preserved RNA to identify specific cell populations; and analyzing mRNA expression patterns of the identified cells by a method comprising: in-situ hybridization; or isolating identified cells and subjecting the isolated cells to bioarray gene profiling. 2. A method according to claim 1, wherein the RNA preservative is selected from the group consisting of triphenylmethane dyes, cresyl violet, polyamines, and cobalt ions. 3. A method according to claim 1, wherein the RNA preservative is a triphenylmethane dye selected from the group consisting of methyl green, crystal violet, and pararosaniline. 4. A method according to claim 1, wherein the histochemically analyzing comprises subjecting the biological sample to a histochemical assay selected from the group consisting of: in situ hybridization for detecting mRNA; fluorescence in-situ hybridization for detecting DNA; immunocytochemistry assay for detecting proteins; enzyme histochemistry assay for measuring catalytic activities of enzymes; ligand-binding autoradiography for studying receptor-ligand interactions; and glycohistochemistry assay for detecting carbohydrate-modified substances.