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Lox stop lox tdtomato reporter mice

Manufactured by Jackson ImmunoResearch

The Lox-stop-lox tdTomato reporter mice are a genetically modified mouse model that express the tdTomato fluorescent protein in a Cre-dependent manner. The mice contain a Lox-stop-Lox cassette that prevents the expression of tdTomato until Cre recombinase is present, which then removes the stop cassette and allows for the expression of the fluorescent reporter protein.

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2 protocols using lox stop lox tdtomato reporter mice

1

Cre-Dependent Neuronal Tracing Using AAV

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Mice between two to six months of either gender were used for experiments. The single-virus method used Gad2-Cre mice (The Jackson Laboratory, stock #028867) or PV-Cre mice (The Jackson Laboratory, stock #017320) with a C57BL/6J background crossed with lox-stop-lox tdTomato reporter mice (The Jackson Laboratory, stock #007914). Mice were injected with 600 nL AAV9.Syn.jGCaMP7f.WPRE. The double-virus method used Gad2-Cre mice (The Jackson Laboratory, stock #028867) or PV-Cre mice (The Jackson Laboratory, stock #017320) with a C57BL/6J background injected with 600 nL AAV9.Syn.jGCaMP7f.WPRE and 200 nL AAV9.FLEX.tdTomato. Viral titer experiments used Gad2-Cre mice specified previously injected with 100 to 300 nL of AAV9.FLEX.tdTomato. Injections were placed stereotaxically at 1.4 mm posterior, +/− 2 mm medial, and 500 μm below Bregma for cortical experiments and 2 mm posterior, +/− 1.4 mm medial, and 1.6 mm below Bregma for hippocampal experiments. A 10 μl syringe (World Precision Instruments) with a 33-gauge needle (NF33BL; World Precision Instruments) injected at 50 nL/min for the somatosensory hip experiments and 100 nL/min for hippocampal experiments controlled by a microsyringe pump (UltraMicroPump 3–4; World Precision Instruments).
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2

Visualizing Layer 2/3 Pyramidal Cells

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To guide electrodes during patch clamp recordings, mice that express the red fluorescent protein tdTomato were used to visualize layer 2/3 excitatory pyramidal cells in somatosensory cortex. C57BL/6J background, CaMKIIa-Cre mice (The Jackson Laboratory, stock #005359; Tsien et al., 1996 (link)) were crossed with the lox-stop-lox tdTomato reporter mice (The Jackson Laboratory, stock #007914; Zariwala et al., 2011 (link)). CaMKIIa promoter in transgenic mice has been established to drive specific expression of fluorescent protein in layer 2/3 pyramidal cells in S1, with expression in ∼32% of pyramidal cells in layer 2/3 (Wang et al., 2013 (link)).
The electrode pipette was visualized using the cyan-green fluorescent dye Alexa Fluor 488 hydrazide (Thermo Fisher Scientific), which was added to the intracellular electrode solution (0.3% weight/volume). Imaging was performed using a two-photon imaging system (Thorlabs) with a mode-locked Ti:Sapphire laser (Chameleon Ultra II; Coherent) set to wavelengths between 920 nm and 950 nm, which was used to excite both the Alexa Fluor 488 and tdTomato using a 20×, NA 1.0 (Olympus) objective lens. Laser scanning was performed using resonant scanners and fluorescence was detected using two photomultiplier tubes (Hamamatsu) equipped with red and green filters to separate emission from Alexa Fluor 488 and tdTomato.
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