Application of environmental sample processor (ESP) methodology for quantifying Pseudo‐nitzschia australis using ribosomal RNA‐targeted probes in sandwich and fluorescent in situ hybridization formats

By D. Greenfield, R. Marin, S. Jensen, E. Massion, B. Roman, J. Feldman, C. Scholin. 2006

90 citations recorded by the source corpus.

Subfields: Analytical Chemistry, Biomaterials, Environmental Chemistry

View Paper: https://www.semanticscholar.org/paper/25ba43188428f4792bd07cb754300c4f96fafbb6

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In Environmental Chemistry

1. R. Marin
2. B. Roman
3. D. Greenfield
4. S. Jensen
5. G. Doucette
6. C. Scholin

Citations in the corpus

• Field applications of the second‐generation Environmental Sample Processor (ESP) for remote detection of harmful algae: 2006‐2007 (2008, methodology): “australis assay was considered potentially quantitative given the established standard curve (Greenfield et al. 2006).”
• Remote, subsurface detection of the algal toxin domoic acid onboard the Environmental Sample Processor: Assay development and field trials (2009, methodology): “Development of the array printing protocol was initiated in 2006, at which point 12 mm diameter disks of Predator1 membrane (Pall Corp., East Hills, NY, USA) were printed using a custom-built arrayer printing 100 nL spots (4 25 nL touches per spot; for details see Greenfield et al., 2006).”