Publications by authors named "Silvan Kaufmann"

Article Synopsis
  • Solanaceae pollen cryopreservation helps the hybrid seed production industry overcome geographical and seasonal challenges, while monitoring pollen quality is crucial to prevent seed yield loss.
  • This study evaluated various pollen quality analysis methods, including viability, germinability, and vigor assessments, on cryopreserved tomato and pepper pollen.
  • The findings indicate that Impedance Flow Cytometry (IFC) is the best method for high-volume applications due to its automation and reliability, while in vitro germination tests are more suited to controlled conditions and vigor tests lack consistency.
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Impedance flow cytometry (IFC) is a versatile lab-on-chip technology which enables fast and label-free analysis of pollen grains in various plant species, promising new research possibilities in agriculture and plant breeding. Hazelnut is a monoecious, anemophilous species, exhibiting sporophytic self-incompatibility. Its pollen is dispersed by wind in midwinter when temperatures are still low and relative humidity is usually high.

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The determination of cell viability is essential to many areas of life sciences and biotechnology. Typically, cell viability measurements are based on the optical analysis of stained cells, which requires additional labeling steps and is hard to implement online. Frequency-dependent impedance flow cytometry (IFC) provides a label-free, fast, and reliable alternative to determine cell viability at the single cell level based on the Coulter principle.

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A sequence-specific oligonucleotide detection method based on the tail-to-tail aggregation of functionalized gold nanoparticles in the presence of target analytes is presented together with its optimization and capabilities for detection of single nucleotide polymorphisms (SNPs). In this single-step method, capture probes are freely accessible for hybridization, resulting in an improved assay performance compared to substrate-based assays. The analytes bring the nanoparticles close to each other via hybridization, causing a red shift of the nanoparticle plasmon peak detected by a spectrophotometer or CCD camera coupled to a darkfield imaging system.

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