Literature DB >> 7199056

Antibodies to the Golgi complex and the rough endoplasmic reticulum.

D Louvard, H Reggio, G Warren.   

Abstract

Rabbits were immunized with membrane fractions from either the Golgi complex or the rough endoplasmic reticulum (RER) by injection into the popliteal lymph nodes. The antisera were then tested by indirect immunofluorescence on tissue culture cells or frozen, thin sections of tissue. There were may unwanted antibodies to cell components other than the RER or the Golgi complex, and these were removed by suitable absorption steps. These steps were carried out until the pattern of fluorescent labeling was that expected for the Golgi complex or RER. Electron microscopic studies, using immunoperoxidase labeling of normal rat kidney (NRK) cells, showed that the anti-Golgi antibodies labeled the stacks of flattened cisternae that comprise the central feature of the Golgi complex, many of the smooth vesicles around the stacks, and a few coated vesicles. These antibodies were directed, almost entirely, against a single polypeptide with an apparent molecular weight of 135,000. The endoplasmic reticulum (ER) in NRK cells is an extensive, reticular network that pervades the entire cell cytoplasm and includes the nuclear membrane. The anit-RER antibodies labeled this structure alone at the light and electron microscopic levels. They were largely directed against four polypeptides with apparent molecular weights of 29,000, 58,000, 66,000, and 91,000. Some examples are presented, using immunofluorescence microscopy, where these antibodies have been used to study the Golgi complex and RER under a variety of physiological and experimental condition . For biochemical studies, these antibodies should prove useful in identifying the origin of isolated membranes, particularly those from organelles such as the Golgi complex, which tend to lose their characteristic morphology during isolation.

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Year:  1982        PMID: 7199056      PMCID: PMC2112017          DOI: 10.1083/jcb.92.1.92

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  31 in total

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2.  Intracellular localization of liver sugar nucleotide glycoprotein glycosyltransferases in a Golgi-rich fraction.

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3.  On the preparation and some properties of closed membrane vesicles from hog duodenal and jejunal brush border.

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4.  The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique.

Authors:  R C Graham; M J Karnovsky
Journal:  J Histochem Cytochem       Date:  1966-04       Impact factor: 2.479

5.  Transient holes in the erythrocyte membrane during hypotonic hemolysis and stable holes in the membrane after lysis by saponin and lysolecithin.

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Journal:  J Cell Biol       Date:  1967-01       Impact factor: 10.539

6.  The labelling of proteins to high specific radioactivities by conjugation to a 125I-containing acylating agent.

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Journal:  Biochem J       Date:  1973-07       Impact factor: 3.857

7.  A technique for ultracryotomy of cell suspensions and tissues.

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Journal:  J Cell Biol       Date:  1973-05       Impact factor: 10.539

8.  Cytochemical localization of 5'-nucleotidase in subcellular fractions isolated from rat liver. I. The origin of 5'-nucleotidase activity in microsomes.

Authors:  C C Widnell
Journal:  J Cell Biol       Date:  1972-03       Impact factor: 10.539

9.  The role of the Golgi complex in sulfate metabolism.

Authors:  R W Young
Journal:  J Cell Biol       Date:  1973-04       Impact factor: 10.539

10.  Synthesis of the carbohydrate of mucus in the golgi complex as shown by electron microscope radioautography of goblet cells from rats injected with glucose-H3.

Authors:  M Neutra; C P Leblond
Journal:  J Cell Biol       Date:  1966-07       Impact factor: 10.539

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  172 in total

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7.  Nucleic acid binding and intracellular localization of unr, a protein with five cold shock domains.

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8.  Increase in the expression of a family of small guanosine triphosphate-binding proteins, rab proteins, during induced phagocyte differentiation.

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9.  Monoclonal antibody against ependymoma-derived cell line.

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10.  Molecular mechanism of mitotic Golgi disassembly and reassembly revealed by a defined reconstitution assay.

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