Characterization of transgenic mice.

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Characterization of transgenic mice. Characterization of transgenic mice. (A) Map of RIP‐SVV transgenic construct. Restriction sites are indicated. (B) Genotyping. Two independent founder lines of RIP‐SVV transgenic mice (#25 and #34) or a PCR‐negative mouse (#9) were analysed by PCR. C, control plasmid DNA; M, molecular weight marker; NT, non‐transgenic. (C) Protein expression. Non‐transgenic (NT) or RIP‐SVV transgenic islets (lines #25 and #34) were analysed by western blotting. NIH3T3 fibroblasts (3T3) or MCF‐7 breast carcinoma cells were used as negative or positive control, respectively. (D–G) Immunohistochemistry. Pancreas sections from RIP‐SVV #34 transgenic mice were stained with antibodies to survivin (D) or insulin (E). Sections of non‐transgenic pancreas were stained for insulin (F) or survivin (G). Magnification, × 200. (H) Glucose levels. Non‐transgenic (NT) or RIP‐SVV transgenic mice (lines #25 and #34) were analysed under feeding or fasting conditions. The results are from two experiments (Expt.). (I) Glucose tolerance test. Non‐transgenic (NT) or RIP‐SVV transgenic mice (three animals/transgenic line, #25 and #34) were analysed. ns, not significant. (J) Kinetics of insulin release. Fasting non‐transgenic or RIP‐SVV transgenic mice (three animals/transgenic line) were analysed. Differences between groups were not statistically significant. (K) Islet size. Insulin‐stained sections of pancreas from RIP‐SVV transgenic mice (TG) or control non‐transgenic (NT) littermates were quantified by morphometry. Each point corresponds to an individual determination. The average islet size was 8,845±651 μm2 (RIP‐SVV, n=114) or 8,964±860 μm2 (non‐transgenic, n=96), P=0.91. (L) Islet number. Ten individual fields of insulin‐labelled pancreas sections from RIP‐SVV or non‐transgenic littermates were analysed by light microscopy (magnification × 200). Data are the mean±s.e.m. Takehiko Dohi et al. EMBO Rep. 2006;7:438-443 © as stated in the article, figure or figure legend