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  • Microtubule  (2)
  • Articular cartilage  (1)
  • Glutamate-specific antiserum  (1)
  • 1
    ISSN: 1432-1106
    Schlagwort(e): Glutamate-specific antiserum ; Immunocytochemistry ; Primary sensory neurons ; Rat
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary We found that large cells in the dorsal root and trigeminal ganglia contained glutamate-like immunoreactivity. Immunoreactive neurons were not detected in the superior cervical or pterygopalatine ganglia. These findings indicated that glutamate is a neurotransmitter or neuromodulator of large cells of sensory ganglia.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1615-6102
    Schlagwort(e): Arabidopsis thaliana ; Cortical microtubules ; Cytoskeleton ; Green-fluorescent-α-tubulin 6 fusion protein ; Microtubule ; Transgenic plant
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary AGFP-TUA6 (α-tubulin 6) gene was transduced in theArabidopsis thaliana genome, and the GFP-TUA6 protein was expressed by 20% of the total α-tubulin amount. The expressed GFP-TUA6 protein was incorporated into cortical microtubules (cMTs), so that the cMTs could be visualized under the fluorescence microscope in the living cells. The rearrangement of cMTs was observed at the tangential epidermal cell face of the hypocotyl. At the initial stage of light-induced cMT rearrangement from a transverse to an oblique or a longitudinal orientation, randomly oriented short MTs appeared. These MTs rapidly elongated obliquely or longitudinally as the transverse cMTs shortened. Finally, the transverse cMTs were replaced by the newly organized oblique or longitudinal cMTs. Reorganization of the cMTs took 50–70 min. Treatment of seedlings with 5 × 10−5 M cytochalasin B induced disarrayed cMTs. The involvement of cytochalasin B in the orientation of developing MTs is discussed.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Protoplasma 206 (1999), S. 201-206 
    ISSN: 1615-6102
    Schlagwort(e): Cytoskeleton ; Epidermal cell ; GFP-TUA6 fusion protein ; Microtubule ; Transgenic plants ; Tubulin
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Summary Microtubules (MTs) were visualized in living cells of several tissues in transgenicArabidopsis thaliana. The transformed Arabidopsis plant was obtained by infecting it withAgrobacterium tumefaciens carrying the GFP-TUA6 plasmid. The fluorescence of the MTs was due to the fluorescence of GFP-TUA6 that was polymerized into the MTs. The distribution patterns of the visualized MTs in the living epidermal cells of leaves was similar to that in fixed epidermal cells. The actual destruction of MTs by oryzalin was observed in a living cell. Cytochalasin B exerts no effect on the distribution pattern of MTs. The fluorescence intensity of MTs was different among cells in different tissues.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Hoboken, NJ [u.a.] : Wiley-Blackwell
    Journal of Orthopaedic Research 7 (1989), S. 344-351 
    ISSN: 0736-0266
    Schlagwort(e): Cryopreservation ; Articular cartilage ; Chondrocytes ; Cell culture ; Transplantation ; Life and Medical Sciences
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Medizin
    Notizen: For osteochondral allograft transplantation to be successful, chondrocytes must survive preservation and retain their capacity to produce normal matrix components: proteoglycans and Type II collagen. Clinical success with osteochondral allograft transplantation has created an increased demand for supplies of suitable cartilage-bearing grafts. This demand has stimulated attempts to find successful methods for low temperature storage of cartilage for “banking” and heightened interest in cartilage cryobiology. In order to achieve the maximum viability of cryopreserved articular cartilage, previous comprehensive studies have focused on rates and temperatures of freezing, cryoprotective agents, and methods and influences of thawing. This study presents evidence that cryopreserved articular chondrocytes maintain their ability to grow in tissue culture following thawing and to produce normal matrix components. Chondrocytes isolated from Japanese white rabbits were divided into groups of fresh controls and experimental cryopreserved cells. Cells were incubated in dimethylsulfoxide, frozen at a rate of -1°C/min, stored at -79°C, rapidly thawed, and plated for culture, Growth rates were comparable in all groups. In all groups, typical chondroid characteristics were maintained throughout 14 days of culture. Typical cartilage phenotypic characteristics included maintenance of polygonal and rhomboidal cells, cell aggregation, proteoglycan production, and Type II collagen synthesis. This investigation strongly indicates that articular chondrocyte cryopreservation yields viable, functional cells and although these results cannot be directly extrapolated to intact adult articular cartilage, they do give further support for low temperature banking of cartilage-bearing allografts for transplantation.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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