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  • tissue culture  (8)
  • Springer  (8)
  • American Institute of Physics (AIP)
  • Nature Publishing Group
  • Wiley
  • 2020-2023
  • 1990-1994  (8)
  • 1991  (8)
Collection
Publisher
  • Springer  (8)
  • American Institute of Physics (AIP)
  • Nature Publishing Group
  • Wiley
Years
  • 2020-2023
  • 1990-1994  (8)
Year
  • 1
    ISSN: 1573-5044
    Keywords: conifer ; cytokinin ; organogenesis ; Picea glauca ; tissue culture ; white spruce
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Picea glauca (white spruce) zygotic embryos and one-week-old-seedling epicotyl explants were placed on either Woody Plant Medium (WPM) or half-strength Schenk & Hildebrandt (1/2S&H) medium supplemented with varying levels of benzyladenine (BA) (0.1, 1.0, 10, 50, 100 μM), zeatin (10, 50, 100 μM) or thidiazuron (TDZ) (0.01, 0.1 μM). In addition to differences in the number of buds induced at three months on the two media, buds induced on WPM were visually more uniform, less vitrified and elongated faster. On 1/2S&H supplemented with BA, maximum bud induction from embryos occurred on 1.0 μM BA with 0.01 μM TDZ with higher BA concentrations inhibitory to bud induction. In contrast, on WPM there was little difference in the number of buds induced from embryos placed on 10, 50 and 100 μM BA with or without TDZ. One-week-old-seedling epicotyl explants required higher BA levels on 1/2S&H, as bud induction at three months was greatest at 10 μM BA. On WPM, as with the embryos, there were only minor differences in the number of buds induced from epicotyl explants on the various BA levels. Zeatin was more effective at inducing buds than BA with both media. From embryos, bud induction was greatest on 50 or 100 μM zeatin without TDZ and 50 or 100 μM zeatin with or without TDZ on 1/2S&H and WPM respectively. From epicotyl explants on 1/2S&H, there was little difference in the number of buds induced with the zeatin concentrations used, while with WPM, 50 and 100 μM zeatin induced the greatest number of buds. Interestingly, with BA, the epicotyl explants needed a higher level than the embryos for maximal response, while with zeatin, the level was the same for both embryos and epicotyl explants. Long-term (six month) survival was higher on WPM than with 1/2S&H. Additionally, embryos had a higher percentage of genotypes surviving at six-months when compared with epicotyl explants. For overall survival and development of the buds, 50 μM zeatin with 0.01 μM TDZ was the best treatment tested.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Methods in cell science 13 (1991), S. 149-161 
    ISSN: 1573-0603
    Keywords: tissue culture ; sharks ; epithelia ; chloride transport ; kidney tubules ; cell regulation ; cystic fibrosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Methods are described for establishing primary monolayer cultures from chloride-secreting epithelial cells of the dogfish shark (Squalus acanthias) rectal gland (SRG). After stimulation, cultures display exceptionally high rates (150 to 250μA/cm2) of transepithelial chloride secretion. Hormones and neurotransmitters which increase cytoplasmic cyclic AMP, cyclic GMP, calcium or phospholipid-derived second messengers are potent secretagogues. Cultures can be analyzed using a variety of morphologic, biochemical, and electrophysiologic methods. These characteristics make SRG cultures a powerful model for delineating the molecular basis of the transmembrane and intracellular signaling networks that stimulate or inhibit secondary active chloride transport in epithelia. Secondary active chloride transport occurs in a variety of epithelia, including those comprising both the proximal and distal segments of vertebrate nephrons.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 17 (1991), S. 167-174 
    ISSN: 1573-1561
    Keywords: Allelopathy ; Antennaria microphylla ; small everlasting ; Euphorbia esula ; leafy spurge ; tissue culture ; hydroquinone ; arbutin ; glucosyltransferase ; biotransformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Callus and suspension cultures ofAntennaria microphylla (small everlasting) and the noxious weedEuphorbia esula (leafy spurge) can glucosylate benzene-1,4-diol (hydroquinone) to the corresponding monoglucoside, arbutin. HPLC analysis of extracts from callus tissue corroborates the presence of hydroquinone in the cells of small everlasting. Constitutive levels of a UDPG-dependent glucosyltransferase were detected in cell-free extracts of this tissue. Although this detoxification enzyme was induced in leafy spurge suspension culture cells grown in the presence of hydroquinone, the activity was six-fold lower than that measured in small everlasting. Differential ability to detoxify hydroquinone provides a basis for the observed allelopathic interaction between small everlasting and leafy spurge.
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  • 4
    ISSN: 1573-5117
    Keywords: callus ; cell culture ; domestication ; protoplast ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cellular biotechnology is a promising application in the propagation and selection of superior strains of seaweeds. Although axenic cultures, organogenetic tissue cultures, vegetative micro-propagation, callus induction and high yields of agar from calli have been described for several species of Gelidium, a number of basic problems remain to be solved. These include standardized methods for obtaining axenic cultures, identification of requirements for organic nutrients, PGR's, cellular disorganization and reorganization, somaclonal variation and somatic incompatibilities. Future progress in seaweed biotechnology will depend on the resolution of many of these problems.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-0603
    Keywords: tissue culture ; uterine epithelial cells ; bovine ; monolayer culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Bovine epithelial cells were obtained for culture from the uterine endometrium of adult, cyclic cattle. Using the procedures described herein, cell-specific monolayers of uterine epithelial cells developed rapidly in culture and maintained a good level of viability for seven to eight subcultures. In addition, frozen-thawed uterine epithelial cells also maintained a respectable level of viability during postthaw subculture. Patterns of cell growth for uterine epithelial cells were determined by a growth curve. A growth curve of fresh epithelial cells over an 8-day interval revealed a short lag phase (24 h) followed by a log growth phase for 5 days and then a stationary phase starting on Days 6 or 7 of incubation. This method for isolation and culture of uterine epithelial cells provides a potential model for evaluating uterine epithelial cell secretory capacity during the estrous cycle. This culture system may offer benefits for in vitro culture of bovine embryos.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 27 (1991), S. 7-14 
    ISSN: 1573-5044
    Keywords: plant regeneration ; propagation ; tissue culture ; viticulture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Shoot apical meristems were used to establish regenerative axillary bud cultures of 9 muscadine grape cultivars. Meristems taken from 10 cm long shoots had less contamination (3%) and a higher survival rate (94%) than those from shorter or longer shoots. Of media tested, MS, 1/2 MS, and C2D resulted in equivalent shoot proliferation rates, whereas, WPM produced stunted shoots. When pooling results for 3 cultivars, 5, 10 and 20 μM BA and 5 μM TDZ produced the highest average number of shoots per cultured apex (3.4–3.8). However, shoots produced with TDZ were stunted and did not root well. For rooting of shoots directly in potting mix, a rooting powder pretreatment significantly increased the number of roots per shoot but did not affect percent rooting or root length. For rooting in vitro, 1 μM NAA significantly increased all parameters measured. Although more shoots rooted in vitro than in vivo (77% vs. 46%), the latter was judged preferable since acclimatized plants were produced in less time and a major culture step was eliminated. Significant differences among cultivars were noted for measured responses in all experiments.
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  • 7
    ISSN: 1573-5044
    Keywords: disease resistance ; Helminthosporium oryzae ; rice ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Rice cultivars showed differential reaction to various isolates of Helminthosporium oryzae, the brown spot pathogen. The calluses obtained from those cultivars behaved in a similar manner to the mycelial growth of pathogenic isolates on them. However, amount of inoculum, size of the callus and period of incubation influenced the reaction of the callus to the fungal isolates.
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  • 8
    ISSN: 1573-0778
    Keywords: tissue culture ; lung cancer ; cytogenetics ; cytotechnology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract This paper describes a tissue culture and exfoliative cell culture system that enables one to (1) evaluate the adequacy of primary lung carcinoma cultures for cytogenetic analysis, and (2) predict the likelihood of viable cells and type of differentiation present in the primary lung tumor cultures used for cytogenetics. Primary lung carcinomas were established from explant outgrowths and maintained in serum supplemented or serum free media on plastic or basement membrane associated protein coated dishes in order to obtain cells for karyotypic analysis (Miura et al., 1990). The media from these cultures that would ordinarily have been discarded was aspirated at each media change and used to prepare cytocentrifuge cytology preparations. Papanicolaou stained cells from the preparations were evaluated by cytotechnologists in order to assess (1) the cellularity and presence of cancer cells in the sample, (2) differentiation of the malignant cells, and (3) adequacy for chromosomal studies. We determined that cytology preparations of cell and explant outgrowth cultures from primary lung tumors are a reliable method for screening and evaluating the suitability of primary lung carcinoma cultures for cytogenetic analysis.
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