Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states were studied by cryo-electron microscopy. High resolution images with good contrast were obtained. As judged from direct images and from the comparison of optical diffractograms with X-ray diffraction patterns obtained from glycerinated muscle fibres, the vitrified specimen is well preserved. Preparation artifacts encountered in conventional plastic sections are avoided. The preservation of the relaxed structure also seems better than in freeze-etched replicas as the 14.5 nm repeat of crossbridges on thick filaments is easily visible
Preparation of biological samples for transmission electron microscopy is not a trivial task. The sa...
A rapid cooling/cryotransfer system was designed to achieve a high reproducibility in vitrifying thi...
A rapid cooling/cryotransfer system was designed to achieve a high reproducibility in vitrifying thi...
Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states...
Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states...
Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states...
Synchrotron radiation was used for low-angle X-ray diffraction to monitor structural changes produce...
A great deal of information on the 3-dimensional structure of the protein assemblies involved in mus...
A great deal of information on the 3-dimensional structure of the protein assemblies involved in mus...
Electron micrograph images of rapidly frozen suspensions of thick filaments from four different musc...
Electron micrograph images of rapidly frozen suspensions of thick filaments from four different musc...
This paper presents electron microscopy, supported by optical diffraction and filtering of images fr...
The preparation and high resolution observation of frozen hydrated thin sections has been studied by...
The preparation and high resolution observation of frozen hydrated thin sections has been studied by...
Preparation of biological samples for transmission electron microscopy is not a trivial task. The sa...
Preparation of biological samples for transmission electron microscopy is not a trivial task. The sa...
A rapid cooling/cryotransfer system was designed to achieve a high reproducibility in vitrifying thi...
A rapid cooling/cryotransfer system was designed to achieve a high reproducibility in vitrifying thi...
Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states...
Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states...
Frozen hydrated sections of vitrified unstained insect flight muscle in the rigor and relaxed states...
Synchrotron radiation was used for low-angle X-ray diffraction to monitor structural changes produce...
A great deal of information on the 3-dimensional structure of the protein assemblies involved in mus...
A great deal of information on the 3-dimensional structure of the protein assemblies involved in mus...
Electron micrograph images of rapidly frozen suspensions of thick filaments from four different musc...
Electron micrograph images of rapidly frozen suspensions of thick filaments from four different musc...
This paper presents electron microscopy, supported by optical diffraction and filtering of images fr...
The preparation and high resolution observation of frozen hydrated thin sections has been studied by...
The preparation and high resolution observation of frozen hydrated thin sections has been studied by...
Preparation of biological samples for transmission electron microscopy is not a trivial task. The sa...
Preparation of biological samples for transmission electron microscopy is not a trivial task. The sa...
A rapid cooling/cryotransfer system was designed to achieve a high reproducibility in vitrifying thi...
A rapid cooling/cryotransfer system was designed to achieve a high reproducibility in vitrifying thi...