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WormBase Tree Display for RNAi: WBRNAi00086321

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Name Class

WBRNAi00086321HomolHomol_homolY73B6BL:RNAi
Sequence_infoDNA_textatggcttcggtggcggcgtggctgccgttcgcgagagccgccgctatcggatgggttcccatttcgagacagcccatgccacaggccccagttgcaatacaggccaaagacctcgcggttgatcatgtctctgacgaaaaactagcaatcaacatatcaggacgaaggttcgaaacgtggaagaacacgttggaaaagttcccagagactctattggggtcaaatgaaaaagagttcttttatgatgaagacactggggaatactttttcgatagggatccggacatattccgacacattctcacattttatagaacgggaaaattgcattatccccgtcatgaatgtcttgttgcatacgacgaagagctcagtttctttggaataatgcctgatttgatatcagattgttgctatgaagactataaagataaaaaacgagaaaatcaagaaagattacaagaagaacgtgtagaaaatgcggatatatcaacattaaaattgtctcttaaagagaaaatgtgggcggcattcgagaatccgcacacaacatcaatagcacttgtattttattatgtcattggattttttattgctgtatcagtgatgtgtaatatagtggaaacaataccttgtgggtatgaggataatgtgtctgtgacgtgtggagaagcctatgaagagcaattctttgttatcgatacagcgtgtgttatcatttttacgattgagtactttttacggttgatttctgcgccggaccgaatcaaatttatgaggtcaataatgagtgtaatcgatgtgattgccataatgccttactacgttagtttggtactaactgacaataaggatgtatccggcttgtttgtcactttaagagttttccgtgtcttccgaatattcaaattctcacgacattcccaaggtcttcgaattctgggttacactcttaaatcgtgtgcaagtgaacttggattccttgtattttcactggcaatggcaattatcatatttgccactattatgtattatgcggagaaaaaggtcgacgcgacgagatttacctcgattccgtcagctttctggtatacaattgtgactctaacaactcttggatacggagacatggttccatcaacaataatgggtaaaatagttggaggagtatgctcactgtctggagtgttggttattgctcttccagttccagttattgtcagcaatttctctcgaatttatcatcaaaatcagagagctgacaagagaaaagcacagaagaaagcccgtcttgctagaattcggatcgttaaaaacgcgtctggactagcattattcaataagaagagagctcatgaagctcggatgctagcatttgaacagggtcatctctctttcgatgctctccgagacgaagatatcttcgaaatccaacatcatcatcttcttcagtgtctagaaaaagcgacggaacgtgaatttgttgaatcagaagtgatgtttgaaggtggaagaaatactcctccgcccagtgaaacagcttcattgaaaggaaaaacaaagcgtaaaaggcgattatgctgtgtttcaaaagaaaatgaagaaatggaagagttggatcgagagactcgtgtaacattcaatcagaatatggatcagatttgtgaattaccaaaacctgatgaaatggaactcaatcatcgaaataatgacaaaatttgcgtatcgcaactatggaaatataaaattgaagtaaaattaactttttatgtgcagttttttttttttcaattttccaggtctgtcgataaagttttatttattttctaa
ExperimentLaboratoryLY
Date09 Aug 2006 00:00:00
TreatmentDouble-stranded RNA (dsRNA) was synthesized byusing standard methods. Cultured myocytes were plated in L-15 control medium or L-15 medium containing 15 micrograms/ml dsRNA final volume. One hour after plating, the dsRNA was diluted to a final concentration of 5 micrograms/ml. Media containing the dsRNA were replaced each day. Electrophysiological experiments were performed 24 days after plating the cells.
Delivered_bySoaking
InhibitsPredicted_geneY73B6BL.19Inferred_automaticallyRNAi_primary
GeneWBGene00022240Inferred_automaticallyRNAi_primary
TranscriptY73B6BL.19.1Inferred_automaticallyRNAi_primary
SpeciesCaenorhabditis elegans
ReferenceWBPaper00028359
Phenotype_not_observedWBPhenotype:0001315RemarkThere was no significant difference in the amplitudes of normalized sustained currents between N2 myocytes and the shl-1 RNAi-treated myocytes
RemarkExact sequence used for RNAi not stated by authors, spliced coding region sequence of gene used for curation.
MethodRNAi