Figure 1 | Scientific Reports

Figure 1

From: Store-operated Ca2+ entry in primary murine lung fibroblasts is independent of classical transient receptor potential (TRPC) channels and contributes to cell migration

Figure 1

Representative images of PCR fragments obtained from genomic DNA of primary murine fibroblasts (pmLF) using gene specific primers separated by agarose gel electrophoresis (a,b). Wild-type (Wt), Stim1/2flox/flox (Stim1fl, Stim2fl) as well as Stim1/2flox/flox fibroblasts infected with lentiviruses expressing Cre recombinase (Stim1fl+Cre, Stim2fl+Cre) were analyzed. (a) DNA fragments amplified from Wt (Wt), Stim1flox/flox (Stim1fl) or deleted Stim1 (Stim1Δ) alleles are marked. (b) DNA fragments amplified from Wt (Wt), Stim2flox/flox (Stim2fl) or deleted Stim2 (Stim2Δ) alleles are marked.

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