#161
Trafficking Pathways in Root Tip

Stephanie Robert (P.I.: Natasha Raikhel and Zhenbiao Yang)

Jae-Ung Hwang and Shundai Li

It is known that there are genetic links between auxin transport and the endomembrane system. The screen was to examine directly the localization of PIN2::PIN2-GFP by Pathway HT automated imaging workstation. It is a fully integrated system for performing high throughput confocal imaging experiments on slides, dishes or multiwell plates. SCREEN DETAILS: For the screen a total of 2016 diverse chemicals were screened. The library was the Selected chemicals from Microsource Spectrum (SP). It was screened at a concentration of 50-100uM in 400ul of medium using our custom chemical 48-well plates. Seeds were germinated on media with chemicals, and PIN2-GFP localization was observed after 5 days. Overall, chemical compounds that altered marker localization or/and cell shape at least for two repetition, were selected. SUMMARY STATISTICS: Of the 2016 chemicals screened, a total of 163 (7.9%) were selected after the first observation (primary screen). After a repetition, 49 chemicals (2.4%) were confirmed in altered PIN2-GFP localization/expression.

NSF: 2010-0520325

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  • Verification in Followyes Additional Verificatio

In total, 1 compound from 1 library is annotated. Out of these, 3 have a score of 1 or higher, and 0 are annotated as inactive.


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Screen strategy

#15324
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LibraryMicrosource Spectrum
ID01504017
NameSAPINDOSIDE-A
FormulaC41H66O12
Molecular Weight 750.956
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Assay 1: 2

#8809
Assay 1: visual phenotype
  • Description None
  • Score 2: active in primary and secondary screen
  • Concentration 50-100 uM (25 ug/ml) in 0.5% DMSO

irregular cell shape

50-100 um chemical (left) compared to DMSO control (right). Results: irregular cell shape

#164
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