Figure 1
Figure 1. Analysis of VSMC-specific TF-deficient mice. (A) Genomic DNA was isolated from the tails of TFflox/flox mice (lane 1), TFflox/flox/SM22αCre+/− mice (lane 2); and TFflox/+/SM22αCre+/− mice (lane 3). PCR was performed with primers that identify the wild-type and floxed TF alleles and the Cre recombinase. (B) mRNA was isolated from brain, lung, and kidney of TFflox/flox (F) and TFflox/flox/SM22αCre+/− (C) mice and analyzed by RT-PCR for TF. GAPDH was used as an internal control for equal loading.

Analysis of VSMC-specific TF-deficient mice. (A) Genomic DNA was isolated from the tails of TFflox/flox mice (lane 1), TFflox/flox/SM22αCre+/− mice (lane 2); and TFflox/+/SM22αCre+/− mice (lane 3). PCR was performed with primers that identify the wild-type and floxed TF alleles and the Cre recombinase. (B) mRNA was isolated from brain, lung, and kidney of TFflox/flox (F) and TFflox/flox/SM22αCre+/− (C) mice and analyzed by RT-PCR for TF. GAPDH was used as an internal control for equal loading.

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