Detection of non-polyadenylated RNA molecules using Turtle Probes and target primed rolling circle PRINS-5

Copyright information:Taken from "detection of non-polyadenylated RNA molecules using Turtle Probes and target primed rolling circle PRINS"http://www.biomedcentral.com/1472-6750/7/69BMC Biotechnology 2007;7():69-69.Published online 18 Oct 2007PMCID:PMC2203993. probe TP-polyA-id33. (B) Dete...

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Hauptverfasser: Stougaard, Magnus, Lohmann, Jakob S, Zajac, Magdalena, Hamilton-Dutoit, Stephen, Koch, Jørn
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Lohmann, Jakob S
Zajac, Magdalena
Hamilton-Dutoit, Stephen
Koch, Jørn
description Copyright information:Taken from "detection of non-polyadenylated RNA molecules using Turtle Probes and target primed rolling circle PRINS"http://www.biomedcentral.com/1472-6750/7/69BMC Biotechnology 2007;7():69-69.Published online 18 Oct 2007PMCID:PMC2203993. probe TP-polyA-id33. (B) Detection of the SSA4-3'UTR RNA fragment with the probe TP-SSA4end-id16. (C) Combined detection of the HPV16E6a RNA and the SSA4-3'UTR RNA fragment with the probes TP-polyA-id33 (green) and TP-SSA4end-id16 (red). The two probes were co-hybridized, co-amplified, and co-detected with a mixture of Lin16 (red identifier) and Lin33 (green identifier). (D-F) Negative controls as (A) save for the following: (D) No capture oligonucleotide present; (E) No RNA was added; (F) The RNA added lacked the artificial polyA tail (HPV16E6noPA RNA) but otherwise had the same sequence as the HPV16E6a RNA used in (A). A 63× objective was used and scale bar is 50 μm.
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(B) Detection of the SSA4-3'UTR RNA fragment with the probe TP-SSA4end-id16. (C) Combined detection of the HPV16E6a RNA and the SSA4-3'UTR RNA fragment with the probes TP-polyA-id33 (green) and TP-SSA4end-id16 (red). The two probes were co-hybridized, co-amplified, and co-detected with a mixture of Lin16 (red identifier) and Lin33 (green identifier). (D-F) Negative controls as (A) save for the following: (D) No capture oligonucleotide present; (E) No RNA was added; (F) The RNA added lacked the artificial polyA tail (HPV16E6noPA RNA) but otherwise had the same sequence as the HPV16E6a RNA used in (A). 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(B) Detection of the SSA4-3'UTR RNA fragment with the probe TP-SSA4end-id16. (C) Combined detection of the HPV16E6a RNA and the SSA4-3'UTR RNA fragment with the probes TP-polyA-id33 (green) and TP-SSA4end-id16 (red). The two probes were co-hybridized, co-amplified, and co-detected with a mixture of Lin16 (red identifier) and Lin33 (green identifier). (D-F) Negative controls as (A) save for the following: (D) No capture oligonucleotide present; (E) No RNA was added; (F) The RNA added lacked the artificial polyA tail (HPV16E6noPA RNA) but otherwise had the same sequence as the HPV16E6a RNA used in (A). 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(B) Detection of the SSA4-3'UTR RNA fragment with the probe TP-SSA4end-id16. (C) Combined detection of the HPV16E6a RNA and the SSA4-3'UTR RNA fragment with the probes TP-polyA-id33 (green) and TP-SSA4end-id16 (red). The two probes were co-hybridized, co-amplified, and co-detected with a mixture of Lin16 (red identifier) and Lin33 (green identifier). (D-F) Negative controls as (A) save for the following: (D) No capture oligonucleotide present; (E) No RNA was added; (F) The RNA added lacked the artificial polyA tail (HPV16E6noPA RNA) but otherwise had the same sequence as the HPV16E6a RNA used in (A). A 63× objective was used and scale bar is 50 μm.</abstract><pub>figshare</pub><doi>10.6084/m9.figshare.47430</doi><oa>free_for_read</oa></addata></record>
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title Detection of non-polyadenylated RNA molecules using Turtle Probes and target primed rolling circle PRINS-5
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