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Sst flp mice

Manufactured by Jackson ImmunoResearch

The Sst-Flp mice are a genetically engineered mouse model developed by Jackson ImmunoResearch. The mice express the Flp recombinase enzyme under the control of the somatostatin (Sst) gene promoter, which is used to target specific cell populations for genetic manipulation.

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2 protocols using sst flp mice

1

Genetically Distinct SOM Interneuron Subsets

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To label genetically distinct subsets of SOM interneurons, we crossed Sst-Flp mice (catalog #028579, The Jackson Laboratory; He et al., 2016 (link)) with one of the following four Cre recombinase-expressing mouse lines: Calb2-Cre (strain #010774, The Jackson Laboratory; Taniguchi et al., 2011 (link)), Calb1-Cre (strain #028532, The Jackson Laboratory; Daigle et al., 2018 (link)), Chrna2-Cre (Leão et al., 2012 (link)), and Pdyn-Cre (strain #027958, The Jackson Laboratory; Krashes et al., 2014 (link)). Dual-recombinase progeny were then crossed with the RC::FLTG reporter line (strain #026932, The Jackson Laboratory; Plummer et al., 2015 (link)) to create triple-transgenic mice expressing GFP in Cre+/Flp+ cells and tdTomato in Cre/Flp+ cells. We also used X94 and X98 mice (strains #006340 and #006334, The Jackson Laboratory; Ma et al., 2006 (link)) to label previously characterized subsets of L4-projecting and L1-projecting SOM cells, respectively, crossing them with Cre driver lines and the Ai9 tdTomato reporter (strain #007909, The Jackson Laboratory; Madisen et al., 2010 (link)).
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2

Fiber Photometry of VIP/SST Interneurons

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Female and male VIP::Cre;SST::Flp mice (#010908 and 028579, respectively; Jackson Laboratory; heterozygous for both recombinases) were bred in house from crossings of homozygous VIP::Cre; SST::Flp females and Df(16)A+/− males23 for the fiber photometry experiments. Df(16)A+/− male breeders were backcrossed for more than 10 generations on a C57BL/6J background. All mice used for photometry were wildtype at the Df(16)A locus (i.e., Df(16)A+/+).
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