Experiment Details
Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
Col-0 | WT | No treatment | No treatment | No treatment | NA | NA | NA | PCR products were purified by alkaline phosphatase and ExoI | 100.00% | Complete | None | 23762347 |
SALK_039629 | mef32 | T-DNA insertion | NA | Knockout | NA | NA | NA | PCR products were purified by alkaline phosphatase and ExoI | 0.00% | Unedited | Absent | 23762347 |
Col-0 | WT | No treatment | No treatment | No treatment | NA | NA | NA | RNA-seq | 95.59% | High | None | 32098170 |
Col-0 | WT | No treatment | No treatment | No treatment | Normal | Rosette leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 100.00% | Complete | None | 28761003 |
Col-0 | DYW2-GFP-OE1 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Rosette leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 99.00% | High | Similar | 28761003 |
Col-0 | DYW2-GFP-OE2 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Rosette leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 99.00% | High | Similar | 28761003 |