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Full-Text Articles in Biology

Mineralogical Application Of The Ion Microscope Elementary Analysis, A. Havette Mar 1985

Mineralogical Application Of The Ion Microscope Elementary Analysis, A. Havette

Scanning Electron Microscopy

The ion microscope is an instrument which allows the study "in-situ" of polished solid surfaces by means of analysis of secondary ions emitted by the sample, this one being bombarded with neutral or ionized particles.

This instrument is a mass spectrometer and an ion microscope. It is then possible to study elements and their isotopes (mass spectra, counting, isotope abundances...) and to know the distribution of these elements in an area of around one hundred micrometers. Molecular and multicharged ions can be superimposed to elementary ions. Two methods can be used to suppress them but, in any case, it results …


X-Ray Microanalysis Of Biological Tissues - An Examination Of Comparative Specimen Preparation Techniques Using Prostatic Tissue As A Model, J. A. Chandler Mar 1985

X-Ray Microanalysis Of Biological Tissues - An Examination Of Comparative Specimen Preparation Techniques Using Prostatic Tissue As A Model, J. A. Chandler

Scanning Electron Microscopy

A number of reproductive tissues have been investigated by X-ray microanalysis for a large number of elements. These elements occur both free and with many different forms of binding to tissue proteins and cellular constituents. The prostate tissue studied here represents a glandular tissue with both parenchymal and stromal components having different cell types. While no general rule can be applied to the preparative technique for all tissues, it would seem that of all the methods examined here freeze substitution or the use of dehydration fluids combined with subsequent embedding offer the most promising compromise between cryoultramicrotomy and aqueous fixation.


Survival And Growth Of Adult Human Oligodendrocytes In Culture: Scanning Electron Microscopy, Seung U. Kim, Kookmin M. Kim, Giuseppe Moretto, Doo H. Shin Feb 1985

Survival And Growth Of Adult Human Oligodendrocytes In Culture: Scanning Electron Microscopy, Seung U. Kim, Kookmin M. Kim, Giuseppe Moretto, Doo H. Shin

Scanning Electron Microscopy

The oligodendrocytes in culture serve as an important model for the study of demyelination diseases. We have previously originated a method of isolating human oligodendrocytes. In order to establish their three dimensional morphology, scanning electron microscopy of the cultured oligodendrocytes was performed.

The oligodendrocytes bulk isolated from adult human brain were maintained in culture for more than 2 months. At the various periods in culture, the cells were studied by scanning electron microscopy and immunofluorescence staining using marker antibodies for the identification of oligodendrocytes. The three dimensional organization and the surface morphology of the cultured oligodendrocytes were investigated. They displayed …


The Growth Of Fetal Human Sensory Ganglion Neurons In Culture: A Scanning Electron Microscopic Study, Seung U. Kim, Kookmin M. Kim, Giuseppe Moretto, James H. Kim Feb 1985

The Growth Of Fetal Human Sensory Ganglion Neurons In Culture: A Scanning Electron Microscopic Study, Seung U. Kim, Kookmin M. Kim, Giuseppe Moretto, James H. Kim

Scanning Electron Microscopy

Sensory neurons of 8-week human fetal dorsal root ganglia were dissociated into single cells by trypsinization and cultured on coverslips for 4 months, in either serum-containing or serum-free chemically defined media. At different times the cultures were fixed and prepared for scanning electron microscopy. Fetal sensory neurons in culture regenerated axons within 24 hours which were characterized by axonal growth cones at their tips and the neuronal perikarya assumed spherical or a bonnet-like morphology.


The Interphotoreceptor Matrix And The Interphotoreceptor Space Of The Vertebrate Retina, M. H. Bernstein Feb 1985

The Interphotoreceptor Matrix And The Interphotoreceptor Space Of The Vertebrate Retina, M. H. Bernstein

Scanning Electron Microscopy

The interphotoreceptor space (IPS) of the vertebrate retina is the adult corollary of the lumen within the embryonic optic vesicle. The inner limit of the IPS is formed by the intercellular junctions of Muller cells and photoreceptors forming the external limiting membrane (ELM). The apical surface of the retinal pigment epithelium (RPE) is the outer limit of the IPS. Most of the volume of the IPS is occupied by the inner and outer segments of the photoreceptors, with the microvillous processes of the RPE, and the small microvilli of the Muller cells filling lesser portions. SEM of samples fixed in …


Theoretical Considerations On Surface Extended X-Ray Absorption Fine Structure (Exafs), Claudine Noguera Feb 1985

Theoretical Considerations On Surface Extended X-Ray Absorption Fine Structure (Exafs), Claudine Noguera

Scanning Electron Microscopy

We have investigated the following theoretical points relevant to surface EXAFS: proportionality of the signal to the absorption cross section, analysis of the oscillations with the simple EXAFS formula, accuracy in the determination of distances and coordination numbers, transferability of phase shifts and amplitude factors. We describe some of the most used techniques to record the Surface Extended X-Ray Absorption Fine Structure (SEXAFS) oscillations, both the photon induced techniques and the electron induced ones, such as the Auger effect, the total or partial yield, the ion desorption technique, the appearance potential spectroscopy and surface reflection electron loss spectroscopy; and in …


Limits Of Quantitative Microanalysis Using Secondary Ion Mass Spectrometry, Peter Williams Feb 1985

Limits Of Quantitative Microanalysis Using Secondary Ion Mass Spectrometry, Peter Williams

Scanning Electron Microscopy

The limitations on secondary ion micro-analytical performance imposed by ionization probabilities, mass spectrometer transmission, requirements for standards and sputtering artifacts have been investigated. The sensitivity of a modern magnetic mass spectrometer for sputtered B+ from oxidized Si is ~ 10-2 ions detected/atom sputtered. For this sensitivity, it is shown that ion microscopy of a part-per-million impurity is limited in lateral resolution to ~ 1 μm. For a 1% impurity, lateral resolution of ~ 30 nm is achievable. Depth profile analysis at the ppm level requires sample areas ~ 10 μm2. Isotope abundance determinations in volumes ~ …


Fly Ash From Full Scale Trona Injection Studies, Raymond T. Greer, Da-Tong Zhang Jan 1985

Fly Ash From Full Scale Trona Injection Studies, Raymond T. Greer, Da-Tong Zhang

Scanning Electron Microscopy

Sodium sesquicarbonate (NaHCO3-Na2CO3-2H2O) and the mineral trona (NaHCO3-Na2CO3-2H2O) have been utilized as effective dry sorbents for SO2 in flue gas during fossil fuel plant full-scale injection studies conducted at the Cameo Station, Unit 1, of Public Service Company of Colorado near Grand Junction, CO. Microstructural and microchemical characterization studies of fly ash samples from these studies identify decomposition features for these carbonates that relate to the development of satisfactory reaction surface areas for combination with SO2 from flue gas. The major features are non-sulfur bearing microspheres …


Freeze-Drying And Related Preparation Techniques For Biological Microprobe Analysis, Romuald Wróblewski, Joanna Wróblewski, Matti Anniko, Lars Edström Jan 1985

Freeze-Drying And Related Preparation Techniques For Biological Microprobe Analysis, Romuald Wróblewski, Joanna Wróblewski, Matti Anniko, Lars Edström

Scanning Electron Microscopy

An X-ray microanalytical and morphological investigation has been carried out on rapidly frozen, freeze-dried or freeze-substituted tissues. A comparison was made between different embedding and polymerisation procedures following freeze-substitution and freeze-drying. The investigation also included an analysis of specimens infiltrated, embedded and polymerised by ultraviolet irradiation at low temperatures with Lowicryl HM20. The morphological preservation of Lowicryl embedded tissue was adequate for the identification of different cell structures like nuclei, mitochondria, lysosomes and different types of endoplasmic reticulum. X-ray microanalytical investigation of low temperature embedded material displayed an elemental composition of cells and organelles similar to that found in freeze-dried …


Recent Developments In Electrical Microcharacterization Using The Charge Collection Mode Of The Scanning Electron Microscope, D. B. Holt, M. Lesniak Jan 1985

Recent Developments In Electrical Microcharacterization Using The Charge Collection Mode Of The Scanning Electron Microscope, D. B. Holt, M. Lesniak

Scanning Electron Microscopy

There are six distinguishable types of charge collection (CC) signal. Consequently specially designed CC detection systems are needed to obtain e.g. true EBIC and EBIV measurements and make quantitative electrical microcharacterization possible. EBIC and EBIV can arise from fields due to barriers such as p-n junctions or due to changes in doping e.g. p to p+. Materials, defect and device parameters are calculable from these signals. Hot-cold stages are important for temperature dependence studies of contrast, for improving signal to noise ratios and reducing leakage currents. Image processing and pattern recognition methods are vital for rapidly locating and evaluating the …


Applications Of Scanning Electron Microscopy And X-Ray Microanalysis In Inner Ear Pathology, M. Anniko, D. J. Lim, A. Sobin, R. Wróblewski Jan 1985

Applications Of Scanning Electron Microscopy And X-Ray Microanalysis In Inner Ear Pathology, M. Anniko, D. J. Lim, A. Sobin, R. Wróblewski

Scanning Electron Microscopy

Surface pathology of inner ear structures so far described in detail concern cochlear and vestibular hair cells and the stria vascularis. In man, surgical intervention into the inner ear is very uncommon and when performed is in general with the primary objective of destroying the diseased peripheral end organs. The vast majority of inner ear tissue available for use with scanning electron microscopy (SEM) is therefore obtained from animals.

The present paper reviews the progression of surface pathology caused by aminoglycoside antibiotics, acoustic overstimulation and in a guinea pig strain with genetic inner ear disease. The primary site of onset …


Cell Movement And Contraction In Somite Development, Ellen A. G. Chernoff Jan 1985

Cell Movement And Contraction In Somite Development, Ellen A. G. Chernoff

Scanning Electron Microscopy

During somite formation the segmental plate mesoderm, lying on either side of the axial organs, reorganizes into roughly spherical pairs of epithelial structures. This segmentation process includes changes in cell shape and position, cell-cell and cell-substratum adhesive properties and accumulation of extracellular matrix material which proceed down the anterior-posterior axis. Later in somite development the sclerotome region "disperses", migrating around the spinal cord where it produces the cartilage model of the vertebral column. Experimental manipulation of segmentation and sclerotome dispersal with drugs affecting microfilaments, microtubules and calcium-dependent contraction suggest that cells migrate into position, elongate, and undergo apical contraction as …


Ultrastructural Studies Of Crystal-Organic Matrix Relations In Renal Stones, P. -T. Cheng, A. D. Reid, K. P. H. Pritzker Jan 1985

Ultrastructural Studies Of Crystal-Organic Matrix Relations In Renal Stones, P. -T. Cheng, A. D. Reid, K. P. H. Pritzker

Scanning Electron Microscopy

Biochemically the organic matrix of kidney stones contains mucoproteins, mucopolysaccharides, inorganic material and bound water. Morphologically, the organic matrix exists as either amorphous or fibrous forms. We have attempted to critically evaluate results from analytical and morphological studies on stone matrices using light microscopy, histochemistry, x-ray diffraction, scanning electron microscopy, x-ray energy dispersive spectrometry, transmission electron microscopy and selected area electron diffraction.

On the surface of calcium oxalate stones, there are usually large masses of randomly deposited calcium oxalate crystals each coated with organic matrix. Transmission electron microscopy shows these large surface crystals are composed of rows of smaller crystallites …


Electron Beam Induced Damage On Passivated Metal Oxide Semiconductor Devices, S. Görlich, E. Kubalek Jan 1985

Electron Beam Induced Damage On Passivated Metal Oxide Semiconductor Devices, S. Görlich, E. Kubalek

Scanning Electron Microscopy

Electron beam testing of integrated circuits (IC) is currently based on the electron beam induced conductivity in insulators to short the passivation layer and to enable a voltage measurement at covered conductor tracks. However, applying this technique to passivated MOS devices causes severe radiation damage, which was at first explained by primary electrons penetrating into the deep-lying gate oxide. Nondestructive electron beam testing was expected by using low electron energies that do not allow the primary electrons to reach into the gate oxide.

Therefore here the influence of nonpenetrating electron irradiation on the characteristics of passivated NMOS transistors has been …


In Vivo Light Microscopy Of Organs, Robert S. Mccuskey Jan 1985

In Vivo Light Microscopy Of Organs, Robert S. Mccuskey

Scanning Electron Microscopy

High resolution, brightfield and fluorescence, light microscopic methods have been developed for examining living organs in situ. The methods permit study of the rate, duration, magnitude and direction of dynamic histologic, pathologic, physiologic and pharmacologic events. In addition, morphometric analyses of such living preparations can provide basic information needed to evaluate alterations induced by fixation and processing of these organs for electron microscopy. Most organs are amenable to such investigations. In anesthetized animals, the selected organ is trans-and/or epi-illuminated with selected wavelengths of monochromatic light, imaged with water immersion objectives and the resulting monochromatic optical images televised using silicon …


Physics Of The Preparation And Observation Of Specimens That Involve Cryoprocedures, E. Kellenberger, E. Carlemalm, W. Villiger Jan 1985

Physics Of The Preparation And Observation Of Specimens That Involve Cryoprocedures, E. Kellenberger, E. Carlemalm, W. Villiger

Scanning Electron Microscopy

With this introductory chapter we attempt a synthesis of old and new knowledge of the physical principles that govern cryomethods. Interface phenomena determine the increase or decrease of the number of particles observed in frozen-hydrated suspensions because they occupy the air-liquid interface according to their specific balance of hydrophobic versus hydrophilic properties. Biological macromolecules are surrounded by organised water, the hydration shell, that prevents them from sticking to each other. Partial or complete removal of these hydration shells by freeze-drying or freeze-substitution leads to collapses or aggregations. The solvent-induced aggregation is usually decreased by prior cross-linking with adequate chemical fixatives. …


On The Application And Possibilities Of In Vivo Microscopy In Liver Research, E. Wisse, R. S. Mccuskey Jan 1985

On The Application And Possibilities Of In Vivo Microscopy In Liver Research, E. Wisse, R. S. Mccuskey

Scanning Electron Microscopy

In vivo microscopy (IVM) provides a valuable method for studying the histophysiology of the living liver. The method allows observation of living cells in the intact organ of an anesthetized animal with an undisturbed microcirculation, at a magnification and a resolution comparable to normal light microscopy of sectioned material. Due to the absence of preparative procedures, the image differs substantially from histological sections, but it has the advantage of providing us with a reference preparation free of artifacts. In the case of the liver, we have the opportunity to observe directly such details as bile capillaries, intracellular fat droplets, lysosomes, …


Glutaraldehyde Fixation Chemistry A Scheme For Rapid Crosslinking And Evidence For Rapid Oxygen Consumption, Timothy J. A. Johnson Jan 1985

Glutaraldehyde Fixation Chemistry A Scheme For Rapid Crosslinking And Evidence For Rapid Oxygen Consumption, Timothy J. A. Johnson

Scanning Electron Microscopy

The chemical literature suggests that pyridine derivatives are the major reaction products of amine-aldehyde reactions. A scheme is proposed for pyridine synthesis which is derived from a classic synthesis of pyridines from one amine molecule and 3 aldehyde molecules. The pyridine polymers are considered as a major class of cross-links in glutaraldehyde fixed cells. This scheme for pyridine synthesis accounts for the following observations of amine-glutaraldehyde react ions: 1) large quantities of acid are rapidly produced, 2) oxygen uptake occurs at a high rate, 3) a variety of products distinguished by molecular size are rapidly and irreversibly synthesized, and 4) …


Tandem Scanning Reflected Light Microscopy, Mojmir Petran, Milan Hadravsky, Alan Boyde, Martin Mueller Jan 1985

Tandem Scanning Reflected Light Microscopy, Mojmir Petran, Milan Hadravsky, Alan Boyde, Martin Mueller

Scanning Electron Microscopy

Most attempts at optical microscopy of bulk living objects have failed because of reflections from optical components and the object surface, and overlapping of unsharp out-of-focus images with the one (weak) sharp in-focus image. The optical signal in the image plane thus consists of a strong d.c. component, a weak noise and a still weaker signal. Most of the first two components can be suppressed by scanning in concordance with both the illuminating and the image-forming rays. In the first scan the focussed-on-object plane is illuminated only in several very fine discrete spots. In the second scan only that light …


Cryofixation And Cryosubstitution For Routine Work In Transmission Electron Microscopy, H. Sitte, K. Neumann, L. Edelmann Jan 1985

Cryofixation And Cryosubstitution For Routine Work In Transmission Electron Microscopy, H. Sitte, K. Neumann, L. Edelmann

Scanning Electron Microscopy

After a brief review of the present state of the theory of cryofixation, methods and instruments as well as criteria for the application of cryofixation and cryosubstitution in daily routine work in cell biology and medicine are described. Good results are obtainable using liquid nitrogen for impact freezing on highly polished copper surfaces or by plunging into liquefied propane. Based on these results a versatile and safe system for routine plunging and impact freezing for the majority of biomedical objects has been developed. In order to enable ultramicrotomy at ambient temperature a cryosubstitution system according to the Edelmann principle has …


Cryopreparation Of Tissue For Electron Microscopy, John G. Linner, Stephen C. Bennett, Donna S. Harrison, Alton L. Steiner Jan 1985

Cryopreparation Of Tissue For Electron Microscopy, John G. Linner, Stephen C. Bennett, Donna S. Harrison, Alton L. Steiner

Scanning Electron Microscopy

An apparatus able to remove amorphous phase tissue water without recrystallization or rehydration has been produced. Application of this technique to biological samples achieves both the preservation of ultrastructure and the retention of cellular macromolecules and solute without redistribution or modification.

Small pieces of fresh tissue were cryofixed by the method of bounce free metal-mirror freezing on polished copper bars at liquid nitrogen temperature. Tissue samples were then placed under liquid nitrogen in a copper sample holder equipped with a thermocouple and feedback controlled heating circuit. Under liquid nitrogen the sample block was placed in a stainless steel sample chamber …


The State Of Water In The Cell, William Negendank Jan 1985

The State Of Water In The Cell, William Negendank

Scanning Electron Microscopy

A number of scientists in the early 20th century conceived cell water and ions as existing in unique "colloidal" or "bound" states. Work in the 1930's, however, established the assumption that most of cell water and of K exist in a free state like that of a dilute aqueous solution, so that the osmotic activity of cell K serves to balance that of the high concentration of extracellular Na. This assumption underlies theoretical concepts of membrane pumps, Donnan equilibria, and cell potentials, and led to the now classical membrane-osmotic-pump-leak concept of cell ionic distributions and volume maintenance. Nevertheless, the results …


Demonstrable Fixative Interactions, Keith M. Meek, John A. Chapman Jan 1985

Demonstrable Fixative Interactions, Keith M. Meek, John A. Chapman

Scanning Electron Microscopy

Electron-optical examination of reconstituted collagen fibrils fixed with tannic acid and/or glutaraldehyde and positively stained with heavy metal anions and cations reveals distinct changes in the high resolution staining patterns seen in TEM. Correlation with the known sequence data demonstrates that these changes are caused by (a) interaction of the fixative with certain charged groups in the collagen and (b) localized stain-exclusion effects following fixation. We have analysed the positive and negative staining patterns from glutaraldehyde-treated collagen in detail. In positive staining, uptake of staining ions is shown to be inhibited not only at residues known to interact with glutaraldehyde …


Observation Of Colloidal Gold Labelled Platelet Surface Receptors And The Underlying Cytoskeleton Using High Voltage Electron Microscopy And Scanning Electron Microscopy, R. M. Albrecht, J. A. Oliver, J. C. Loftus Jan 1985

Observation Of Colloidal Gold Labelled Platelet Surface Receptors And The Underlying Cytoskeleton Using High Voltage Electron Microscopy And Scanning Electron Microscopy, R. M. Albrecht, J. A. Oliver, J. C. Loftus

Scanning Electron Microscopy

Fibrinogen conjugated to colloidal gold or colloidal gold-monoclonal anti-glycoprotein IIb/IIIa (fibrinogen receptor) was used to label the receptor on platelets. Whole mount preparations were examined by stereo pair high voltage electron microscopy and then by scanning electron microscopy to determine the feasibility of this approach in detecting the number of receptors and their location relative to the cytoskeletal and surface structure. Both the ligand-gold and antibody-gold labels were effective. The relative numbers of receptors could be seen and their relationship to cytoskeletal structure could be determined. Marked differences in receptor number and distribution were observed when platelets in different stages …


Cell Volume Regulation Studies With The Electron Microprobe, Mary Jo Ingram, F. Duane Ingram Jan 1985

Cell Volume Regulation Studies With The Electron Microprobe, Mary Jo Ingram, F. Duane Ingram

Scanning Electron Microscopy

Lumbricals from the hind feet of young rats are dissected free, stretched to approximately 125% of resting length, and mounted on individual, simple plastic forms. After recovery in physiological saline, the isolated muscles are incubated for periods of 40 to 60 min. in one of a series of hypertonic bathing solutions. The composition of each bathing solution is identical, except for osmolality which is increased with lactose. At least one muscle from each animal is incubated in a control solution to serve as a control muscle for that particular set of 5 to 8 muscles. Mounted muscles are removed from …


Does The Embedding Chemistry Interact With Tissue?, B. E. Causton Jan 1985

Does The Embedding Chemistry Interact With Tissue?, B. E. Causton

Scanning Electron Microscopy

Resins and resin compounds interact with tissue in two ways, physico-chemically and by chemical reaction. The physico-chemical influences affect both the structure and biological activity of the tissue causing proteins to change shape or phase equilibria to be disrupted by a change in solvent or by the growth of polymer networks within existing biological polymeric structures. Chemical reactivity between tissue and resin components also reduces biological activity by changing either the structure of polymeric matter already present, e.g., crosslinking proteins, grafting hydrophobic resins onto hydrophilic protein backbones, or by modifying the hydrophobicity of specific sites, e.g., acylation of amino groups …


Two Opposing Theories Of The Cell: Experimental Testing By Cryomethods And Electron Microscopy, L. Edelmann Jan 1985

Two Opposing Theories Of The Cell: Experimental Testing By Cryomethods And Electron Microscopy, L. Edelmann

Scanning Electron Microscopy

A main controversial issue in cell biology concerns the molecular mechanism responsible for K+ accumulation in living cells and Na+ exclusion from them. The alternative theoretical descriptions of these phenomena are based on different assumptions about the physical state of cellular Na+, K+ and H2O. In this article it is shown with striated muscles how cryomethods and microanlytical electron microscopy may be used to test the opposing theories. It is concluded that these methods may yield more realistic informations about the physical state of cellular K+ and Na+ than measurements with …


Complementary Replicas Of Ultra-Rapidly Frozen Specimens, M. J. Costello, R. D. Fetter, T. G. Frey Jan 1985

Complementary Replicas Of Ultra-Rapidly Frozen Specimens, M. J. Costello, R. D. Fetter, T. G. Frey

Scanning Electron Microscopy

Complementary freeze-fracture replicas have been prepared of ultra-rapidly cooled specimens in the absence of chemical pretreatments. The grid-sized replicas were stabilized by open mesh gold grids during the cleaning process and, after cleaning, were supported on thin Formvar films. The complementary replicas were valuable for describing artifacts, for interpreting the nature of fracture planes and for evaluating the resolution of replicas. Complementary images demonstrated that heat emitted from resistance electrodes or electron guns during evaporation can seriously distort fracture surfaces even for samples held at -150°C. Complementary images of crystalline membranous cytochrome c oxidase helped establish that fracturing reveals hydrophilic …


The Glass Knife In Ultramicrotomy, Lahja Sevéus, Cecilia Tarras-Wahlberg Jan 1985

The Glass Knife In Ultramicrotomy, Lahja Sevéus, Cecilia Tarras-Wahlberg

Scanning Electron Microscopy

To obtain the best ultrathin sections in ultramicrotomy and cryoultramicrotomy, a high quality knife is of paramount importance. Glass knives were introduced for ultramicrotomy, in the manually broken form, in 1950. Since the introduction of mechanical knifemakers, the production of glass knives has become a standardized laboratory routine. In conventional ultramicrotomy different knife angles are used to cover different specimens and embedding media. The 50° knife broken with a small deviation of the score from the diagonal of the square gives a long useful edge, especially if damping during breaking is used. The 50° knife is, therefore recommended as the …


Low Temperature Embedding, E. Carlemalm, W. Villiger, J. -D. Acetarin, E. Kellenberger Jan 1985

Low Temperature Embedding, E. Carlemalm, W. Villiger, J. -D. Acetarin, E. Kellenberger

Scanning Electron Microscopy

The Lowicryl resins K4M and HM20 are methacrylate/acrylate based formulations which can re used for embedding biological material at low temperature in conjunction with either the progressive lowering of temperature (PLT) technique or with freeze-substitution. The resins are applicable over a very extended temperature range, approximately 210°K to 340°K. Even lower temperatures down to ca. 190°K can be reached with two new resins, K11M and HM23. Test embeddings of unfixed material after freeze-substitution have given promising results which could re useful for imnunocytochemical labeling. Lipid extraction is small or absent when the two new resins are used in combination with …