474-Yoshinari-NucleiAutofluoNIR/FigS2_NIR_H2B_Arabi_RootMeristem_EpiderCell_Mut
Author reviewed
The time-lapse NIR autofluorescence images of epidermal cells in root meristemetic zone of mutant Arabidopsis expressing H2B-mClover
Dataset ID
FigS2_NIR_H2B_Arabi_RootMeristem_EpiderCell_Mut
Title
The time-lapse NIR autofluorescence images of epidermal cells in root meristemetic zone of mutant Arabidopsis expressing H2B-mClover
Description
The nuclear near-infrared (NIR) autofluorescence was observe the epidermal cells in root meristimetic zone of 4-day-old mutant Arabidopsis expressing H2B-mClover.
Time-lapse NIR autofluorescence imaging visualized epidermal cells in the root meristematic zone of mutant Arabidopsis.
The NIR autofluorescence imaging approach has no need for a fluorescent protein reporter and can reduce the genetic manipulation time of introducing encoded nuclear markers into mutant plants to improve the efficiency of monitoring the cell nuclei movement in root.
Folder Name
FigS2_NIR_H2B_Arabi_RootMeristem_EpiderCell_Mut
Dimensions
1024x1024x15x2x30
Biosample
Description
The 4-day-old trangenic Arabidopsis expressing H2B-mClover was grown on modified MGRL medium containing boric acid for 3 days.
Intrinsic Variable
H2B–mClover was introduced into Arabidopsis thaliana by genetic transformation, resulting in transgenic plants expressing a histone H2B fused to the fluorescent protein mClover.
Ontology
Genetics
Method / Genotype
transgenic
Treatments
Imaging Method
Imaging Method
confocal microscopy
fluorescence microscopy
time lapse microscopy
Visualization Method
H2B-mClover
NIR autofluorescence
Sample Preparation Method
living tissue
Instrument
Light Source
The excitation wavelength was set at 640 nm with 0.90 mW at the back focal plane of the objective and the detection was set at 656–700 nm.
Objective
0.8 NA Plan-Apochromat, Zeiss, Oberkochen, Germany
1.1 NA LD C-Apochromat, Zeiss
1.4 NA Plan-Apochromat, Zeiss