A multicolored set of in vivo organelle markers for co-localization studies in Arabidopsis and other plants.

By B. K. Nelson, Xue Cai, A. Nebenführ. The Plant Journal, 2007

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The FAST technique: a simplified Agrobacterium-based transformation method for transient gene expression analysis in seedlings of Arabidopsis and other plant species (2009, methodology): “px-cb pFGC19 Kanamycin d35S Peroxisome-CFP [25]”
Root-to-shoot Cd translocation via the xylem is the major process determining shoot and grain cadmium accumulation in rice (2009, positive): “S3 in Supplementary data available at JXB online) by co-localization with the peroxisomal marker px-rk (Nelson et al., 2007).”
SUBA4: the interactive data analysis centre for Arabidopsis subcellular protein locations (2016, methodology): “For research, SUBA has contributed to the development of widely used organelle marker sets (11), protein family clone collections for functional genomics (12), as well as facilitated the functional elucidation of protein families involved in plant growth regulation (13).”
Rapid, combinatorial analysis of membrane compartments in intact plants with a multicolor marker set. (2009, background): “Other, more recent attempts have been limited in scope, and have focused on compartments that are already well defined (Nelson et al., 2007).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, positive): “(A) 35S:PhAAE-GFP and (B) the mCherry peroxisomal marker px-rk (Nelson et al., 2007) were co-infiltrated using A.”