File:Figure 7.jpg

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Figure_7: Expression analysis ofGS3using RT–PCR and genetic transformation. (A) RT–PCR ofGS3from Asominori, AIS22, and Nipponbare using young panicles (�3 cm) for RNA extraction. Numbers in parentheses indicate cycles of PCR. Actin cDNA was amplified as a control. (B) RT–PCR ofGS3from Asominori using panicles �3, 5, 7, 10, and 13 cm and after heading and a flag leaf for RNA extraction. (C and D)GUSstaining of transgenic plants transformed with theGS3promotor:GUSfusion construct showing panicles before flowering (C) and a panicle at flowering with a flag leaf (D). Bars, 1 cm.

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current03:04, 30 May 2014Thumbnail for version as of 03:04, 30 May 2014593 × 198 (29 KB)Cloud27 (talk | contribs)Figure 7. Expression patterns of cyclin genes in the OsMYB3R-2 transgenic rice, cold response and survival ratio, and cellular free Pro in the OsCycB1;1 transgenic rice lines. A, Expression patterns of cyclin-responsive genes in wild-type (WT) and OsMYB3R
06:46, 17 May 2014Thumbnail for version as of 06:46, 17 May 2014255 × 580 (17 KB)Cyyhappy1989 (talk | contribs)Figure_7: Expression analysis ofGS3using RT–PCR and genetic transformation. (A) RT–PCR ofGS3from Asominori, AIS22, and Nipponbare using young panicles (�3 cm) for RNA extraction. Numbers in parentheses indicate cycles of PCR. Actin cDNA was amplifie
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