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Ve cad cre

Manufactured by Jackson ImmunoResearch

VE-Cad-Cre is a primary antibody that recognizes the Cre recombinase protein. It is used to detect and visualize the expression of Cre recombinase in cells or tissues.

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2 protocols using ve cad cre

1

Genetically Modified Mouse Models for Investigating LRP5/6 Signaling

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Lrp5-/- [42 (link)] and Lrp5a214v(neo)/+ [21 (link)] mice were generated as described. Lrp5fl/fl and Lrp6fl/fl [22 (link)], Flk1Breier-Cre [30 (link)], Rx-Cre [23 (link)] and CD11b-Cre [29 (link)] mice were kindly provided by Drs. Bart O. William, Kevin P. Campbell, Eric Swindell and Roland Baron, respectively. VE-Cad-Cre [24 (link)], Tie2-Cre [25 (link)], LysM-Cre [28 (link)] and tdTomato [27 (link)] mice were purchased from the Jackson Laboratory. Flk1Breier-Cre, Rx-Cre, CD11b-Cre, VE-Cad-Cre and Tie2-Cre mice were all transgenic lines generated by fusing the Cre gene to a fragment of the promoter sequence of Flk1, Rx, CD11b, VE-Cad and Tie2, respectively. LysM-Cre mice were knock-ins, generated by targeted insertion of the Cre cDNA into the endogenous M lysozyme locus. When animals from different genetic backgrounds were crossed, littermate controls were used to avoid confounding effects.
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2

Endothelium-specific LKB1 Knockout Mice

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Mice expressing the Cre recombinase under control of the VE-Cadherin promoter/enhancer (VE-CAD-Cre) were purchased from Jackson Laboratory.23 (link) LKB1-floxed (LKB1flox/flox) mice were purchased from the National Cancer Institute, which was made by DePinho lab.24 (link) To generate endothelium-specific LKB1endo−/− mice, LKB1flox/flox mice were crossbred with VE-CAD-Cre mice. PCR-based genotyping was performed, as described previously.25 (link) The animals were housed in a controlled environment (20 ± 2°C, 12-h/12-h light/dark cycle), where they were maintained on a standard chow diet with free access to water. Male mice at 3 months of age were subjected to endothelial function analyses and blood pressure measurements. For adenoviral injections, wild-type (WT) or LKB1endo−/− mice received tail vein injections of 100 μL adenoviral vectors that expressed green fluorescent protein (GFP) or constitutively active (CA)-AMPK (4 × 1010 viral particles). The animal protocol was reviewed and approved by the Animal Care and Use Committee at the University of Oklahoma Health Sciences Center.
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