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1.
Sci Rep ; 3: 3497, 2013 Dec 13.
Article in English | MEDLINE | ID: mdl-24336573

ABSTRACT

Sponges are probably the earliest branching animals, and their fossil record dates back to the Precambrian. Identifying their skeletal structure and composition is thus a crucial step in improving our understanding of the early evolution of metazoans. Here, we present the discovery of 505-million-year-old chitin, found in exceptionally well preserved Vauxia gracilenta sponges from the Middle Cambrian Burgess Shale. Our new findings indicate that, given the right fossilization conditions, chitin is stable for much longer than previously suspected. The preservation of chitin in these fossils opens new avenues for research into other ancient fossil groups.


Subject(s)
Chitin , Fossils , Porifera/chemistry , Animals , Biological Evolution , Chitin/chemistry , Polysaccharides/chemistry
2.
Microsc Res Tech ; 69(3): 186-95, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16538624

ABSTRACT

Multidimensional time-correlated single photon counting (TCSPC) is based on the excitation of the sample by a high-repetition rate laser and the detection of single photons of the fluorescence signal in several detection channels. Each photon is characterized by its arrival time in the laser period, its detection channel number, and several additional variables such as the coordinates of an image area, or the time from the start of the experiment. Combined with a confocal or two-photon laser scanning microscope and a pulsed laser, multidimensional TCSPC makes a fluorescence lifetime technique with multiwavelength capability, near-ideal counting efficiency, and the capability to resolve multiexponential decay functions. We show that the same technique and the same hardware can be used for precision fluorescence decay analysis and fluorescence correlation spectroscopy (FCS) in selected spots of a sample.


Subject(s)
Microscopy, Fluorescence, Multiphoton/methods , Cell Line , Cell Nucleus/chemistry , Fluorescence Resonance Energy Transfer , Green Fluorescent Proteins/analysis , Humans , Intracellular Signaling Peptides and Proteins , Microscopy, Confocal/methods , Photons , Protein Kinases/metabolism , Protein Serine-Threonine Kinases , Recombinant Fusion Proteins/analysis , Skin/ultrastructure
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