The present short review aims to give an overview of the most recent developments in fluorescence microscopy and its applications in biomedical sciences. Apart from improvements in well established methods based on co...The present short review aims to give an overview of the most recent developments in fluorescence microscopy and its applications in biomedical sciences. Apart from improvements in well established methods based on conventional fluorescence microscopy and confocal microscopy (fluorescence in situ hybridisation (FISH), tyramide signal amplification (TSA) in immunocytochemistry, new fluorophores), more recently introduced techniques like fluorescence resonance energy transfer (FRET), fluorescence recovery after photobleaching (FRAP), multiphoton microscopy and fluorescence correlation spectroscopy (FCS) will be discussed.展开更多
A novel Hadamard transform(HT) microscopic image detection system which can generate 511× 512 pixel format images of fluorescence or absorptive light for small samples has been developed, when spatial multiplexin...A novel Hadamard transform(HT) microscopic image detection system which can generate 511× 512 pixel format images of fluorescence or absorptive light for small samples has been developed, when spatial multiplexing is performed with a 511 slit one dimensional Hadamard mask and a highly sensitive linear CCD. The weak native fluorescence imaging for Zephyranthes candida (Lindl.) Herb. Pollen cells can be realized within 1 min. The spatial resolution of 0 6 μm per pixel has been achieved with a 40× objective. The imaging speed, sensitivity and spatial resolution are satisfactory, hence the system has a good application prospect in cell biology and medicine. Some factors that influence imaging speed and quality have been discussed preliminarily.展开更多
文摘The present short review aims to give an overview of the most recent developments in fluorescence microscopy and its applications in biomedical sciences. Apart from improvements in well established methods based on conventional fluorescence microscopy and confocal microscopy (fluorescence in situ hybridisation (FISH), tyramide signal amplification (TSA) in immunocytochemistry, new fluorophores), more recently introduced techniques like fluorescence resonance energy transfer (FRET), fluorescence recovery after photobleaching (FRAP), multiphoton microscopy and fluorescence correlation spectroscopy (FCS) will be discussed.
文摘A novel Hadamard transform(HT) microscopic image detection system which can generate 511× 512 pixel format images of fluorescence or absorptive light for small samples has been developed, when spatial multiplexing is performed with a 511 slit one dimensional Hadamard mask and a highly sensitive linear CCD. The weak native fluorescence imaging for Zephyranthes candida (Lindl.) Herb. Pollen cells can be realized within 1 min. The spatial resolution of 0 6 μm per pixel has been achieved with a 40× objective. The imaging speed, sensitivity and spatial resolution are satisfactory, hence the system has a good application prospect in cell biology and medicine. Some factors that influence imaging speed and quality have been discussed preliminarily.
