Rabbit Mating and Embryo Isolation

2010 ◽  
Vol 2010 (1) ◽  
pp. pdb.prot5350-pdb.prot5350 ◽  
Author(s):  
B. Puschel ◽  
C. Viebahn
Keyword(s):  
Embryo Isolation

Gamete and embryo isolation and culture with microfluidics

2007 ◽  
Vol 68 ◽  
pp. S190-S195 ◽  
Author(s):  
G.D. Smith ◽  
S. Takayama
Keyword(s):  
Embryo Isolation

scholarly journals Simple Embryo Isolation Techniques from Ophrys (Orchidaceae) Seeds

2013 ◽  
Vol 3 (6) ◽  
pp. 448-450
Author(s):  
Mehmet Aybeke ◽  
Keyword(s):  
Isolation Techniques ◽  
Embryo Isolation

scholarly journals Rethinking gamete/embryo isolation and culture with microfluidics

2003 ◽  
Vol 9 (5) ◽  
pp. 451-461 ◽  
Author(s):  
R. S. Suh
Keyword(s):  
Embryo Isolation

scholarly journals Tolerance of spring and winter wheats to herbicide in in vitro culture

Pesticidi ◽  
2002 ◽  
Vol 17 (3-4) ◽  
pp. 125-129 ◽  
Author(s):  
Ankica Kondic-Spika ◽  
Radivoje Jevtic
Keyword(s):  
Winter Wheat ◽  
In Vitro Culture ◽  
Embryo Culture ◽  
Fresh Mass ◽  
Percentage Reduction ◽  
Wheat Varieties ◽  
Control Variant ◽  
Embryo Isolation ◽  
Winter Wheat Varieties

Spring and winter wheat varieties have been compared for tolerance to tribenuron in the zygous embryo culture. Four randomply selected varieties of each spring and winter wheat were used for embryo isolation. The embryos were grown for 30 days in a modified MS (Murashige and Skoog, 1962) medium to which tribenuron was added in three different concentrations (18.75 mgl~ 37.50 mgl", 56.25 mgl 1). The percentage of surviving calli and the percentage reduction of callus fresh mass in relation to the control variant served as parameters of tolerance. All of the tested parameters indicated that the winter wheats had a higher level of tolerance to the herbicide than the spring wheats.

scholarly journals Effect of the timing of embryo isolation on the output of seedlings of sour cherry varieties when cultivated in vitro

2020 ◽  
Author(s):  
N. N. Kovalenko ◽  
N. V. Polivara
Keyword(s):  
Sweet Cherry ◽  
Sour Cherry ◽  
Optimal Timing ◽  
Fruit Crops ◽  
Mass Flowering ◽  
Starting Point ◽  
Speed Up ◽  
Embryo Isolation ◽  
Normal Fertilization

The breeders are faced with the task of the fastest breeding of sour cherry (Prunus cerasus L) varieties, which will be able to fill a niche among the insurance stone fruit crops, complementing the existing assortment. It is practically impossible to speed up this process without the use of in vitro culture. In this regard, the purpose of the present study was to identify the most favorable timing for isolating embryos of sour cherry varieties and hybrids with sweet cherry for embryos active development and growth in vitro. Analysis of the literature data and the results obtained in this study allows a conclusion that the timing of embryos isolation for their introduction into in vitro culture plays a very important role for the entire breeding process. Due to the discrepancy in defining the timing, a certain starting point is proposed, which is the date of fertilization (artificial pollination), or mass flowering in the case of free pollination. The parameters (height and width) of sour cherry seeds, which depend on the period of pollination, are given. Together with the cotyledons, the embryos of sour cherry varieties on the 14th day of their development correspond to sizes from 1.2 × 0.4 mm to 1.6 × 1.0 mm and, in the case of normal fertilization, increase in size from 6 .5 × 5.1 mm to 7.2 × 6.3 mm by day 28-30, on an average. At the same time, the seed with the embryo of hybrid sour cherry varieties (dukes) reaches higher values, e.g., 11.3 × 8.1 mm. When introducing cherry embryos into culture, one should focus on their size, as well as on the period that has passed from pollination. It was found that the periods of isolation, both early on day 14-19 and late on day 44-52, negatively affect the development of embryos: they stop their development, and the number of the obtained seedlings decreases. It has been experimentally proven that the most optimal timing of fruit picking for growing cherry hybrids in vitro is the period from day 28 to 32 after pollination of flowers: active development was observed in them on days 10-15 in test tubes, and most of them (83-85%) began to germinate 40 days later (on day 39-47 after the introduction into in vitro culture). In general, this leads to the efficient hybridization and accelerated obtaining of seedlings in the same year.

scholarly journals Two isoforms of eIF-5A in chick embryo. Isolation, activity, and comparison of sequences of the hypusine-containing proteins.

1992 ◽  
Vol 267 (9) ◽  
pp. 6107-6113
Author(s):  
E.C. Wolff ◽  
T.G. Kinzy ◽  
W.C. Merrick ◽  
M.H. Park
Keyword(s):  
Chick Embryo ◽  
Embryo Isolation

scholarly journals Development of breeding lines by zigotic ovule culture in Nigella sativa L.

Genetika ◽  
2021 ◽  
Vol 53 (2) ◽  
pp. 583-591
Author(s):  
Hüseyin Uysal ◽  
Emre Sevindik
Keyword(s):  
Nigella Sativa ◽  
Callus Formation ◽  
Formation Rate ◽  
Culture Technique ◽  
Ovule Culture ◽  
Zygotic Embryos ◽  
Breeding Lines ◽  
Black Cumin ◽  
Catalog Number ◽  
Embryo Isolation

This study was carried out in order to develop an embryo culture technique and to establish breeding lines with this technique. Ovule culture was preferred in the study because the seeds were too small and embryo isolation was difficult. Embryo cultures were done by using populations obtained from producers in Samsun, Denizli, Isparta, Mersin in Turkey and ?ameli black cumin variety. Hybridizations were done according to the semi-diallel hybridization method to gain zygotic embryos. LS2.5 and MS (Sigma Aldrich Catalog number: M5519) mediums were used for ovule culture and MSD4 medium was used growing the plants obtained from the ovules. As a result of the research, a total of 2904 ovules were cultured in LS2.5 medium. 148 of them showed callus development; callus formation rate was 5.10%. The highest callus formation rate in the investigated combinations was obtained from ?ameli x Denizli combination at 7.26%. Plant regeneration could not be obtained from these calluses. A total of 3526 ovules were cultured in MS medium. Sixty plantlets were obtained from these ovules and plant formation rate was determined as 1.70%. 41 plants from these matured and were harvested.

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