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WormBase Tree Display for RNAi: WBRNAi00102337

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Name Class

WBRNAi00102337HomolHomol_homolD2024:RNAi
Sequence_infoPCR_productmv_D2024.7
ExperimentLaboratoryRD
Date07 Jul 2009 00:00:00
GenotypePgstk-1::GFP::GSTK-1
TreatmentRNAi strain cultures were grown for 6 hours in LB medium containing 100 mg/mL ampicillin, and then spread onto NGM agar containing isopropyl thio-beta-D-galactoside (1 mM) and carbenicillin (25 micrograms per millilter). For double- RNAi treatment, equal concentrations of both strains were mixed before seeding. The next day, animals at the fourth larval stage were placed onto RNAi plates, grown for 2 days and then harvested by rinsing with M9 buffer (0.1 M NaCl, 0.05 M potassium phosphate, pH 6.0). Adults were allowed to settle, and eggs were recovered from hermaphrodites by alkaline hypochlorite lysis (5 min at room temperature in 0.5 M NaOH, 5% hypochlorite). The eggs were rinsed with M9 buffer and the resulting L1 larvae were transferred the next day to fresh agar plates containing the different dsRNA conditions.
Delivered_byBacterial_feeding
InhibitsPredicted_geneD2024.7Inferred_automaticallyRNAi_primary
GeneWBGene00017054Inferred_automaticallyRNAi_primary
TranscriptD2024.7.1Inferred_automaticallyRNAi_primary
SpeciesCaenorhabditis elegans
ReferenceWBPaper00035091
Phenotype_not_observedWBPhenotype:0000306Remarkgstk-2 RNAi does not affect expression of the GFP::GSTK-1 transgene
Remark(Figure S1B) gstk-2 RNAi
MethodRNAi