On detection of pseudo‐nitzschia (bacillariophyceae) species using whole cell hybridization: sample fixation and stability
By P. Miller, C. Scholin. 2000
97 citations recorded by the source corpus.
Subfields: Environmental Chemistry, Molecular Biology, Oceanography
View Paper: https://www.semanticscholar.org/paper/385b96ee52134f94376106a443a3241a0b08ad37
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In Environmental Chemistry
In Molecular Biology
In Oceanography
Citations in the corpus
- Identification and enumeration of Alexandrium spp. from the Gulf of Maine using molecular probes (2005, methodology): “While the ethanol-SET fixation method of Miller and Scholin (2000) is amenable to shipboard use and does not use hazardous chemicals such as formalin and methanol, the preserved specimens have a shelf life of only 4–6 weeks.”
- LIFE CYCLE OF THE HETEROTROPHIC DINOFLAGELLATE PFIESTERIA PISCICIDA (DINOPHYCEAE)1 (2002, methodology): “In situ hybridization with PNA probes was performed using reagents, filter apparati, and protocols adapted from methods established by Miller and Scholin (1998, 2000) for oligonucleotide probes.”
- Domoic acid in phytoplankton and fish in San Diego, CA, USA (2006, methodology): “The abundances of P. australis and P. multiseries were estimated using fluorescent in situ hybridization (FISH) in a filter-based whole cell format (Scholin et al., 1996; Miller and Scholin, 1996, 1998, 2000), which utilizes a species-specific molecular probe with a fluorescent tag.”
- INTRASPECIFIC GENETIC DIVERSITY IN THE MARINE COCCOLITHOPHORE EMILIANIA HUXLEYI (PRYMNESIOPHYCEAE): THE USE OF MICROSATELLITE ANALYSIS IN MARINE PHYTOPLANKTON POPULATION STUDIES 1 (2006, background): “…that the diversity detected with these neutral markers exceeds that of other slower-evolving DNA markers (Gallagher 1982, Scholin et al. 1994, Miller and Scholin 2000) and are consistent with DNA fingerprinting techniques, including microsatellites, used for the analysis of marine planktonic…”
- 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 (2006, methodology): “The manifold designed for laboratory use is described elsewhere (Miller and Scholin 1998, 2000).”