Figure 2
Lattice LSFM of transgenic Arabidopsis plants carrying diverse genetically encoded molecular markers which are developmentally and subcellularly regulated in bulging trichoblasts and in outgrowing root hairs. A, ANN1-GFP as a cytosolic marker, (B, Supplemental Video S5) GFP-RHD2 as endosomal and apical PM marker and (C) GFP-FABD2 as actin cytoskeleton marker. Bar = 10 µm (A–C). Imaging: W Plan-Apochromat 25×/1.1 NA, excitation at 488 nm at 75% relative laser power, detection with BP520/30 (a bandpass filter transmitting an emission from 505 to 535 nm), the pixel size 104 nm/pixel, z-stacks of 0.5 µm/plane, encompassing the volume of ∼50.5 µm, exposure time 50 ms, and full stack acquisition 5.3 s.

Lattice LSFM of transgenic Arabidopsis plants carrying diverse genetically encoded molecular markers which are developmentally and subcellularly regulated in bulging trichoblasts and in outgrowing root hairs. A, ANN1-GFP as a cytosolic marker, (B, Supplemental Video S5) GFP-RHD2 as endosomal and apical PM marker and (C) GFP-FABD2 as actin cytoskeleton marker. Bar = 10 µm (A–C). Imaging: W Plan-Apochromat 25×/1.1 NA, excitation at 488 nm at 75% relative laser power, detection with BP520/30 (a bandpass filter transmitting an emission from 505 to 535 nm), the pixel size 104 nm/pixel, z-stacks of 0.5 µm/plane, encompassing the volume of ∼50.5 µm, exposure time 50 ms, and full stack acquisition 5.3 s.

Close
This Feature Is Available To Subscribers Only

Sign In or Create an Account

Close

This PDF is available to Subscribers Only

View Article Abstract & Purchase Options

For full access to this pdf, sign in to an existing account, or purchase an annual subscription.

Close