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11.
An apparatus suitable for the recovery of proteins from polyacrylamide gels on a milligram scale by displacement electrophoresis (isotachophoresis) is described along with a buffer system that is suitable for this purpose with most proteins. The technique is illustrated by the recovery of a protein from a 15% polyacrylamide gel. The recovery was almost quantitative and the eluted protein showed little contamination upon quantitative amino acid analysis and automatic Edman degradation. 相似文献
12.
Östermann Elisabeth Sternberger Nancy H. Sternberger Ludwig A. 《Cell and tissue research》1983,228(3):459-473
Among a total of 135 tissue-reactive monoclonal antibodies previously prepared, 81 were brain-selective and were classified into neuronal and non-neuronal categories. The neuronal antibodies were again subdivided into antineurofibrillar, antiperikaryonal-neurofibrillar, and antisynapse-associated groups. On the basis of morphologic, developmental, biochemical, and pathologic criteria, the antibodies in at least two of these groups were found to detect heterogeneous antigens (called "neurotypes") rather than different antigenic determinants in single antigens. On examining the distribution in peripheral organs of staining patterns of 11 antineuronal brain-reactive antibodies, we now confirm that these antibodies are, indeed, largely brain-specific. In general, non-neuronal elements in liver, lung, heart, thymus, intestine, adrenal, and spleen remained unstained. However, most of the antibodies stained peripheral neural elements. Occasional antibodies did stain selected, non-neuronal structures. Four out of five antineurofibrillar antibodies stained nerve fibers in adrenal medulla, intestine and thymus. All of three antiperikaryonal-neurofibrillar antibodies also stained nerve fibers in the adrenal medulla, but not in other organs. Two out of three antisynapse-associated antibodies stained what appear to be nerve contacts on adrenal medullary cells, but not on any other peripheral cells examined. The non-neuronal peripheral staining patterns were restricted to selective nuclear staining exhibited by two out of five antineurofibrillar antibodies and the staining of macrophage and selected cardiac muscle nuclei by two of three antisynapse-associated antibodies. However, one antineurofibrillar antibody also stained the cytoplasm of selected liver cells. Among non-neuronally reacting antibodies, two antibodies stained nuclei of all cells except neurons in brain as well as peripheral organs. An antibody staining the ciliary epithelium of choroid plexus also stained basal bodies of ciliated bronchial epithelium. The overall data suggest that the specificity of brain-reactive antibodies is high and that their cross-reactivity with epitopes in non-nervous tissue is rare. In these cases, the antibodies seem to provide specific reagents for these additional structures as well as for their specific brain antigens. 相似文献
13.
Some observations on coleoptile cell ultrastructure in ungerminated grains of rice (Oryza sativa L) 总被引:1,自引:0,他引:1
Helgi Öpik 《Planta》1971,102(1):61-71
Summary The ultrastructure of coleoptile cells of ungerminated rice grains has been examined following fixation in glutaraldehyde and osmium tetroxide. In many respects the cell structure resembles that reported for other dormant seed tissues: the cells contain protein bodies and lipid droplets, mitochondria and plastids show little internal structure but cytoplasm invaginates into many plastids; golgi cisternae cannot be discerned. Rough ER is present as cisternae surrounding protein bodies, as occasional regions of parallel layers, and in concentric whorls where it alternates with smooth paired membranes of an unknown nature. The ribosomes on the ER are at least partly arranged into regular rows. Various crystalline, presumably proteinaceous, inclusions lie in the groundplasm, plastids and nuclei. 相似文献
14.
In a variety of tumour systems, individuals carrying progressively growing neoplasms have lymphoid cells with a specific cytotoxic effect on cultured tumour cells from the same individual1–4. Since the sera of tumour-bearing individuals have been shown to prevent tumour cell destruction by immune lymphocytes in vitro2,5–8 and since this serum blocking activity appears early in primary and transplant tumour development5,7, it has been suggested that the appearance of this serum blocking activity might be responsible for the progressive growth of tumours in individuals having cytotoxic lymphocytes. Counteraction of this blocking activity would thus be of primary importance in facilitating the function of an already existing or bolstered cell-mediated immunity. The serum blocking activity might be inhibited in various ways, by preventing the formation of blocking antibody or by interfering with its action (“unblocking”), as demonstrated in Moloney sarcoma regressor sera9. This type of serum also has a therapeutic effect on Moloney sarcomas in vivo10,11, which has been tentatively attributed to its unblocking activity8,9 or, possibly, to a complement-dependent cytotoxicity10. Tumour growth in the Moloney sarcoma system, however, might be due in part to continuous recruitment of neoplastic cells by virus-induced transformation and so the therapeutic effect could be due to a virus-neutralizing serum activity9,10. 相似文献
15.
Association of Viral Reverse Transcriptase with an Enzyme degrading the RNA Moiety of RNA-DNA Hybrids 总被引:44,自引:0,他引:44
K. MÖLLING D. P. BOLOGNESI H. BAUER W. BÜSEN H. W. PLASSMANN P. HAUSEN 《Nature: New biology》1971,234(51):240-243
DURING replication of RNA tumour viruses, the genetic information contained in the viral RNA seems to be transferred to DNA1,2. Studies on the enzymatic activities present in the virus particles suggest that this transfer is mediated by an RNA dependent DNA polymerase3,4. RNA-DNA hybrids have been demonstrated to occur as intermediates in this reaction5 and single stranded DNA is generated as an early reaction product6, which is then replicated to give a double stranded DNA product6–8. The mechanism by which the single stranded DNA is displaced from the RNA template is, however, not known. 相似文献
16.
DURING each step of peptide chain elongation the ribosome shifts up one triplet along the messenger RNA with concomitant movement of the peptidyl-transfer RNA from the donor to the acceptor site. This process, commonly known as translocation, is triggered by a supernatant protein, factor G, which in association with the ribosome cleaves GTP into GDP and inorganic phosphate1,2 and it has been argued that the energy liberated in this reaction is used “to carry the complex one triplet forward”3. 相似文献
17.
Polyacrylamide gel electrophoretic patterns of soluble proteinsfrom intact potato tubers and from wounded tuber tissue wereidentical. The patterns from diseased tissue showed some minordifferences not before 34 days after inoculation. Itis concluded that primarily proteins of minor fractions areinvolved in protein synthesis after wounding or infection. (Received March 22, 1969; ) 相似文献
18.
On the percentage points of the sample coefficient of variation 总被引:2,自引:0,他引:2
19.
Ohne Zusammenfassung 相似文献
20.
Summary A dichromatic contact microradiographic method is presented for quantitative microanalysis of lead in mineralized tissues utilizing the L absorption edges of lead. Sections of mineralized tissue with a thickness of about 100 are exposed to filtered molybdenum K and copper K radiation. Quantitative localization of lead is possible within small areas of the order of 50
2 with an accuracy of 25 · 10–12g lead. The method has been applied to studies of long term accumulation of lead in bone tissue. 相似文献