456-Ezaki-FESEMCellProlife/Fig3A_5dasLeafPrimordia_an3_04
Author reviewed
Z-series images of 5 DAS leaf primordia of an3 mutant-Arabidopsis thaliana_sample4 stained with BCECF-AM (vacuole) and FM4-64 (plasma membrane)
Dataset ID
Fig3A_5dasLeafPrimordia_an3_04
Title
Z-series images of 5 DAS leaf primordia of an3 mutant-Arabidopsis thaliana_sample4 stained with BCECF-AM (vacuole) and FM4-64 (plasma membrane)
Description
The 5 DAS leaf primordia of an3 mutant-Arabidopsis thaliana sample4 stained with BCECF-AM, used as the fluorescent indicator for vacuole, and FM4-64, used as the dye for plasma membrane. Z-series images were obtained by confocal microscopy.
The size and shape of vacuole in the mutant an3 were larger and more unified.
The ANGUSTIFOLIA (AN3) gene is a positive regulator of cell proliferation and an3-4 allele was isolated by Horiguchi et al. (2005).
Folder Name
Fig3A_5dasLeafPrimordia_an3_04
Dimensions
1024x1024x56x2x1
Biosample
Description
The leaf primordia was cut from a 5 DAS an3 mutant-Arabidopsis thaliana seedling. The vacuoles were stained with BCECF-AM. The plasma membranes were stained with FM4-64.
Intrinsic Variable
In the an3-4 strain, ANGUSTIFOLIA (AN3) gene is mutated. It was identified by screening for leaf-shape mutants in M2 populations generated by fast neutron bombardment and X-ray irradiation.
Ontology
Genetics
Method / Genotype
radiation induced mutation
Protein / Probe
-BCECF-AM
Treatments
Imaging Method
Visualization Method
fluorescent label
Imaged Parameter
fluorescence emission
Sample Preparation Method
living tissue
Instrument
Body
Olympus-Evident FV3000
Light Source
BCECF was excited with a laser at 488 nm, and the emission was detected between 500 and 570 nm.
For FM4-64, the excitation wavelength was 514 nm, and emission was detected between 600 and 640 nm.