scholarly journals A transformation system for CLP with dynamic scheduling and CCP

1997 ◽  
Author(s):  
Sandro Etalle ◽  
Maurizio Gabbrielli ◽  
Elena Marchiori
Keyword(s):  
Dynamic Scheduling ◽  
Transformation System

scholarly journals A transformation system for CLP with dynamic scheduling and CCP

1997 ◽  
Vol 32 (12) ◽  
pp. 137-150 ◽  
Author(s):  
Sandro Etalle ◽  
Maurizio Gabbrielli ◽  
Elena Marchiori
Keyword(s):  
Dynamic Scheduling ◽  
Transformation System

Dynamic Scheduling of Post-Earthquake Emergency Material Based on the Baseline Perspective

CICTP 2020 ◽  
2020 ◽  
Author(s):  
Ziqi Tang ◽  
Hui Hu ◽  
Guangyuan Yang ◽  
Rundong Wu
Keyword(s):  
Dynamic Scheduling

Dual priority dynamic scheduling algorithm based on multi-FPGA

2013 ◽  
Vol 33 (3) ◽  
pp. 862-865
Author(s):  
Shuangzhi DU ◽  
Yong WANG ◽  
Xiaoling TAO
Keyword(s):  
Dynamic Scheduling ◽  
Scheduling Algorithm

Development of an Agrobacterium-mediated Transformation System for `Beurre Bosc' Pear

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 461d-461
Author(s):  
Richard L. Bell ◽  
Ralph Scorza ◽  
Chinnathambi Srinivasan
Keyword(s):  
Shoot Proliferation ◽  
Induction Medium ◽  
Shoot Induction ◽  
Transformation System ◽  
Gus Histochemical Assay ◽  
Young Leaves ◽  
Leaf Tissues ◽  
Shoot Induction Medium ◽  
Basal Salts

An efficient regeneration/transformation system was developed for `Beurre Bosc' pear. Young leaves were harvested from in vitro shoots proliferated on a medium containing MS basal salts and 5 BAP, 0.5 μM IBA, and 0.6M3. Shoot regeneration was optimized using a modification of the medium of Chevreau and Leblay (1993). Explants were cultured on shoot induction medium contained 10 μM TDZ and 1 μM IBA for 4 weeks in the dark, and then transfered to a similar, but auxinless, regeneration medium until shoots developed, usually after an additional 4 to 8 weeks. Leaf tissues were transformed by co-cultivation for 3 days with Agrobacterium tumefaciens EHA101 carrying a pGA482 plasmid containing NPTII, GUS, and rolC genes, followed by cultivation on SIM containing 300 mg/L timentin. Putative transgenic plants were selected on shoot induction medium containing 80mg/L kanamycin, and multiplied on shoot proliferation medium. Four clones were confirmed as transgenic using the GUS histochemical assay and Southern blots for the NPTII and rolC genes. Plants of each clone have been rooted and successfully transfered to the greenhouse for further analysis of gene expression.

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