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Strain Species Genotype
NF591 C. elegans mig-22(tk24) III. Show Description
DTC migration defect.
NF68 C. elegans mig-22(k141) III. Show Description
DTC migration defect.
BC10306 C. elegans dpy-5(e907) I; sEx10306. Show Description
sEx10306 [rCes PAR2.4::GFP + pCeh361]. Maintain by picking WT. WT animals are GFP+. Strain construction supported by Genome British Columbia and Genome Canada. Please acknowledge McKay et al, Cold Spring Harbor Symposia on Quantitative Biology 68: 159-169 2004 (WBPaper00006525).
NF1226 C. elegans mig-22(tk69) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). Show Description
mig-22(tk69): DTC migration defect and maternal effect embryonic lethal. Heterozygotes are WT with pharyngeal GFP signal. Homozygous hT2[bli-4 let-? qIs48] are inviable.