Maize Genomics and Genetics 2012, Vol.3, No.1, 1
-
5
ISSN 1925-1971 http://mgg.sophiapublisher.com
5
Figure 7 The construction of pHorD-
GBSS
Ⅰ
expression vector
gene of plant expression vector, specific premiers were
designed. Primer sequences are as follows: Test-F:
5'
-
AGAACAGACCAAGATACAAACG
-
3'; Test-R:
5'
-
ATAGGGACGAGGCGAAGA
-
3'. Used the geno-
mic DNA extracted from leaves of regenerated plant as
template to detect the
bar
gene in the regenerated
plants. PCR amplification was carried out with the
specific primers, which were designed based the
fragments of
GBSS
Ⅰ
gene and promoter
HorD
. Took
the recombinant plasmid pHorD-
GBSS
Ⅰ
as the
positive control, the untransformed plants as negative
control, and H
2
O as blank control, we detected by
PCR method.
Author contributions
Rongxi Zhou and Ying Wu are the executors of experimental
design and experimental study, Hongda Zou is the guidance of
the vectors design, Hongkui Liu assisted transplant seedlings
and provided technical post-management, Shipeng Li and
Xiaohui Shan guided and analyzed the single-post test data and
wrote the first draft paper; Shengzhong Su involved in the
experimental design; Yaping Yuan is in charge of the project
and experimental idea who participated in experimental design
and wrote and modified the paper. All authors have read and
agreed the final text of this article.
Acknowledgements
The research was funded by the National GMO Cultivation of
New Varieties of Major Projects fund (2009ZX08003
-
024B).
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