Fig. 1
 Histochemical GUS staining and fluorometric assay of the  PLA 2 -γ  promoter. (A) Diagram of the  PLA 2 -δ  and  PLA 2 -γ  genomic region. The gray dotted lines indicate the untranslated regions, the black boxes indicate the exons, and black bold lines indicate the introns. (B) Diagram of the  PLA 2 -γ  promoter and its 5′-deletion series. Numbers indicate the distance in nucleotides from the translational start codon. (C) Histochemical GUS staining of flowers of three independent T 3 homozygous Arabidopsis lines transformed with  ProPLA 2 -γ  : GUS or its deletion constructs. Flowers in this figure display the representative phenotypes of each line. (D) Fluorometric GUS activity assay of flowers in three independent T 3 transgenic lines. Flowers of a wild-type plant were used as a negative control. Error bars show ± SD ( n = 3).

Histochemical GUS staining and fluorometric assay of the PLA 2 promoter. (A) Diagram of the PLA 2 and PLA 2 genomic region. The gray dotted lines indicate the untranslated regions, the black boxes indicate the exons, and black bold lines indicate the introns. (B) Diagram of the PLA 2 promoter and its 5′-deletion series. Numbers indicate the distance in nucleotides from the translational start codon. (C) Histochemical GUS staining of flowers of three independent T 3 homozygous Arabidopsis lines transformed with ProPLA 2 : GUS or its deletion constructs. Flowers in this figure display the representative phenotypes of each line. (D) Fluorometric GUS activity assay of flowers in three independent T 3 transgenic lines. Flowers of a wild-type plant were used as a negative control. Error bars show ± SD ( n = 3).

Close
This Feature Is Available To Subscribers Only

Sign In or Create an Account

Close

This PDF is available to Subscribers Only

View Article Abstract & Purchase Options

For full access to this pdf, sign in to an existing account, or purchase an annual subscription.

Close