PMC:17597 / 14713-15721 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/17597","sourcedb":"PMC","sourceid":"17597","source_url":"http://www.ncbi.nlm.nih.gov/pmc/17597","text":"Labeling and hybridization\nDNA probes were generated from 5 μg total RNA by reverse transcriptase synthesis (Superscript II enzyme, Life Technologies), using oligo-dT primers and biotin-labeled dUTP and dATP (in a 1:10 molar ratio to unmodified dTTP and DATP, respectively). Probes were cleaned by spin filtration, denatured, and then incubated in hybridization buffer (50% formamide, 6 × SSPE, 0.5% SDS, 5 × Denhardt's solution) with 0.1 pmol poly-(A)25 for 2 h at 42°C. Hybridization was carried out at 42°C, followed by a series of stringency washes, as in [3]. Membranes were washed, bathed in the Avidx alkaline-phosphatase conjugate then exposed to the chemiluminescent substrate CDP-star, according to the manufacturer's instructions (Tropix, Applied Biosystems). Membranes were next exposed to autoradiographic film for between 10 min and 8 h. Each membrane was used only once, giving an independent hybridization for 2 embryo replicates, 4 bipotential larvae, 13 queen, and 13 worker larval samples.","divisions":[{"label":"Title","span":{"begin":0,"end":26}}],"tracks":[{"project":"2_test","denotations":[{"id":"11178278-10318926-44706710","span":{"begin":561,"end":562},"obj":"10318926"}],"attributes":[{"subj":"11178278-10318926-44706710","pred":"source","obj":"2_test"}]},{"project":"Colil","denotations":[{"id":"T26","span":{"begin":561,"end":562},"obj":"10318926"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/docs/sourcedb/PubMed/sourceid/"}],"attributes":[{"subj":"T26","pred":"source","obj":"Colil"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"2_test","color":"#93ecbb","default":true},{"id":"Colil","color":"#eca193"}]}]}}