460-Tanaka-RadialAxisDyn/Fig3B_hdg11_12pdf2
Author reviewed
The time-lapse images of observing in vitro-cultivated hdg11/12 pdf2 ovules expressing WOX2p::H2B-GFP and WOX2p::LTI-tdTomato
Dataset ID
Fig3B_hdg11_12pdf2
Title
The time-lapse images of observing in vitro-cultivated hdg11/12 pdf2 ovules expressing WOX2p::H2B-GFP and WOX2p::LTI-tdTomato
Description
The marker WOX2p::H2B-GFP to label the embryo nucleus of Arabidopsis and the marker WOX2p::LTI-tdTomato to label the plasma membrane (PM) showed that after the zygote division the apical cell of in vitro-cultivated hdg11/12 pdf2 ovules expands to take on a special shape before dividing vertically.
The pdf2 mutant was introduced into the hdg11/12 mutant to get the hdg11/12 pdf2 triple mutant.
Folder Name
Fig3B_hdg11_12pdf2
Dimensions
512x512x11x2x256
Biosample
Description
The embryo nucleus of Arabidopsis vitro-cultivated hdg11/12 pdf2 ovules was labelld by the markers WOX2p::H2B-GFP and WOX2p::LTI-tdTomato.
Intrinsic Variable
The marker WOX2p::H2B-GFP was to label the embryo nucleus, and the marker WOX2p::LTI-tdTomato was to label the plasma membrane (PM) of Arabidopsis.
In the hdg11/12 pdf2 ovules, HDG11 (homeodomain glabrous11), HDG12 (homeodomain glabrous12) and PDF2 (protodermal factor2 ) lose their function by transfer DNA (T-DNA) insertion.
Ontology
Genetics
Method / Genotype
transgenic
Protein / Probe
Hydrophobic protein RCI2B
Method / Genotype
transgenic
Method / Genotype
transgenic
Method / Genotype
transgenic
Method / Genotype
transgenic
Treatments
Imaging Method
Imaging Method
spinning disk confocal microscopy
Detection Method
spot detector
Visualization Method
Green fluorescent protein from Aequorea
tdTomatoFP
Imaged Parameter
fluorescence emission
Sample Preparation Method
living tissue
Instrument
Body
Yokogawa Electric
CSU-W1