- WBPaper00045263:ProLongevity-mtROS_downregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly decreased expression under all of these conditions
- [cgc6390]:Cluster_F
hierarchical clustering
Germline-enriched and sex-biased expression profile cluster F.
- WBPaper00045263:ProLongevity-mtROS_upregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly increased expression under all of these conditions
- WBPaper00045263:0.1mM-paraquat_upregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly increased expression after treatment with 0.1mM paraquat vs. control
- WBPaper00045263:0.1mM-paraquat_downregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly decreased expression after treatment with 0.1mM paraquat vs. control
- WBPaper00045263:nuo-6(qm200)_upregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly increased expression in nuo-6(qm200) vs. N2, and in nuo-6(qm200);ced-4(n1162) vs. ced-4(n1162).
- WBPaper00045263:isp-1(qm150)_downregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly decreased expression in isp-1(qm150) vs. N2, and in isp-1(qm150)ced-4(n1162) vs. ced-4(n1162).
- WBPaper00045263:isp-1(qm150)_upregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly increased expression in isp-1(qm150) vs. N2, and in isp-1(qm150) ced-4(n1162) vs. ced-4(n1162).
- WBPaper00045263:nuo-6(qm200)_downregulated
Comparisons of each genotype were compared to the wild-type using the Empirical Base (Wright & Simon) algorithm and fold changes were represented on a log2 scale. A threshold of p < 0.05 and a fold change of 1.3 (log2) was set to determine differentially expressed targets.
Transcripts with significantly decreased expression in nuo-6(qm200) vs. N2, and in nuo-6(qm200);ced-4(n1162) vs. ced-4(n1162).
- WBPaper00024704:Soluble_protein
N.A.
Soluble proteins identified according to HPLC electrospray ionization (ESI)-MS-MS, using the method in which the protein mixtures were first derivatized with a water-soluble fluorogenic reagent, SBD-F or 7-chloro-4-(dimethylaminoethylaminosulfonyl)-2,1,3-benzoxadiazole (DAABD-Cl).