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Jackson Laboratory heterozygous sert cre mice
Heterozygous Sert Cre Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sert-cre+mice/cre+jackson+laboratory+mice+sert/bio_rxiv__64898__2025__12__19__695484-31-6-12
Average 86 stars, based on 1 article reviews
heterozygous sert cre mice - by Bioz Stars, 2026-09
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Article Title: Pou3f1 orchestrates a gene regulatory network controlling contralateral retinogeniculate projections.
Article Snippet: Sert-Cre mice (RRID:IMSR_ JAX:014554) were crossed with a Rosa26/CAG-floxed-STOP-tdTomato (referred to as R26-tdTom mice) reporter line (RRID:IMSR_ JAX:007909)62 and both lines were obtained from the Jackson laboratory.

Article Title: Sex-biased effects on hippocampal circuit development by perinatal SERT expression in CA3 pyramidal neurons
Article Snippet: Other mouse lines used for this work were: Thy1-GFP/M mice (Jackson Laboratories 007788) ( Feng et al., 2000 ), SERT-CRE mice (Jackson Laboratories 014554) ( Zhuang et al., 2005 ) and Ai14 Cre-dependent-tdTomato line (Jackson Laboratories 007914) ( Madisen et al., 2010 ).

Article Title: Protocol for in vivo imaging and analysis of brainstem neuronal activity in the dorsal raphe nucleus of freely behaving mice.
Article Snippet: Cell segmentation and data validation from areas with high motion and correlated activity In vivo brainstem imaging with miniature microscopy has been challenging due to surgical difficulty, high motion, and correlated activity between neurons.. Here, we present a protocol for brainstem imaging in freely moving mice using the dorsal raphe nucleus as an example.. We describe surgical procedures to inject a virus encoding GCaMP6m and securely implant a GRIN lens in the brainstem.

Article Title: Raphe serotonin projections dynamically regulate feeding behavior through targeting inhibitory circuits from rostral zona incerta to paraventricular thalamus.
Article Snippet: Animals C57BL/6 J (Strain #: 000664), Sert-Cre (Strain #:014554) [34], and vGAT-Cre (Strain #: 028862) [35] mice were purchased from the Jackson Laboratory and GAD-GFP mice were generously provided by Pradeep G Bhide lab at Florida State University [36].

Article Title: Protocol for in vivo imaging and analysis of brainstem neuronal activity in the dorsal raphe nucleus of freely behaving mice
Article Snippet: For Sert-Cre mice, see these instructions from The Jackson Laboratory.

Article Title: Alcohol inhibits sociability via serotonin inputs to the nucleus accumbens
Article Snippet: Methods 2.1 Animals In these experiments, we used adult male and female C57BL/6J mice from Jackson Labs (Bar Harbor, ME, USA), as well as transgenic Sert-cre (Jackson Labs, 014554), Pdyn-ires-cre (Jackson Labs, 027958), and EGFP-L10a mice (Jackson Labs, 024750) which were bred in-house.

Article Title: Sex-biased effects on hippocampal circuit development by perinatal SERT expression in CA3 pyramidal neurons
Article Snippet: SERT PyramidΔ mice were generated by crossing SERT fl/fl ; Emx1-Cre (Jackson Laboratories 00562) ( Gorski et al., 2002 ) females and SERT fl/fl males.

Article Title: Raphe serotonin projections dynamically regulate feeding behavior through targeting inhibitory circuits from rostral zona incerta to paraventricular thalamus
Article Snippet: C57BL/6 J (Strain #: 000664), Sert-Cre (Strain #:014554) [ ], and vGAT-Cre (Strain #: 028862) [ ] mice were purchased from the Jackson Laboratory and GAD-GFP mice were generously provided by Pradeep G Bhide lab at Florida State University [ ].



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Jackson Laboratory heterozygous sert cre mice
Heterozygous Sert Cre Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory b6.129(cg)- slc6a4 tm1(cre)xz /j (sert-cre) mice
a: Confocal fluorescence micrograph illustrating a section of the PFC of a <t>SERT-Cre::tdTomato</t> adult mouse. Note the dense labeling of deep-layer tdTomato-positive neurons. Scale bar: 500 µm b: Close-up of the micrograph of A showing deep-layer, fluorescent SERT+ cells and shadows of SERT- cells (asterisks). Scale bar: 10 µm. c: Scheme of the experimental procedure. PNFLX protocol was followed by patch-clamp recordings in acute brain slices obtained from adult mice. d: Representative current-clamp traces showing the response to 0.8 s-long current injections from SERT+ and SERT- PNs. Red and orange traces: SERT+ PNs in CTR and PNFLX, respectively. Black and gray traces: SERT- PNs in CTR and PNFLX, respectively. current injections: from -100 to +375 pA in all cases. e: Firing rate vs. current injections in all cases. Same colors as in D. *P < 0.05; **P < 0.01; ***P < 0.001. f: Scheme of the experimental procedure. Same as in C, except that during PNFLX protocol mice received concomitant intraperitoneal injections of saline solution or saline solution containing the 5-HT7 antagonist (SB269970) twice a day. g-h: Same as in d-e but in the presence of SB269970 (SB).
B6.129(cg) Slc6a4 Tm1(cre)xz /J (Sert Cre) Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory sert-cre female mice
a: Confocal fluorescence micrograph illustrating a section of the PFC of a <t>SERT-Cre::tdTomato</t> adult mouse. Note the dense labeling of deep-layer tdTomato-positive neurons. Scale bar: 500 µm b: Close-up of the micrograph of A showing deep-layer, fluorescent SERT+ cells and shadows of SERT- cells (asterisks). Scale bar: 10 µm. c: Scheme of the experimental procedure. PNFLX protocol was followed by patch-clamp recordings in acute brain slices obtained from adult mice. d: Representative current-clamp traces showing the response to 0.8 s-long current injections from SERT+ and SERT- PNs. Red and orange traces: SERT+ PNs in CTR and PNFLX, respectively. Black and gray traces: SERT- PNs in CTR and PNFLX, respectively. current injections: from -100 to +375 pA in all cases. e: Firing rate vs. current injections in all cases. Same colors as in D. *P < 0.05; **P < 0.01; ***P < 0.001. f: Scheme of the experimental procedure. Same as in C, except that during PNFLX protocol mice received concomitant intraperitoneal injections of saline solution or saline solution containing the 5-HT7 antagonist (SB269970) twice a day. g-h: Same as in d-e but in the presence of SB269970 (SB).
Sert Cre Female Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory sert-cre mice
a: Confocal fluorescence micrograph illustrating a section of the PFC of a <t>SERT-Cre::tdTomato</t> adult mouse. Note the dense labeling of deep-layer tdTomato-positive neurons. Scale bar: 500 µm b: Close-up of the micrograph of A showing deep-layer, fluorescent SERT+ cells and shadows of SERT- cells (asterisks). Scale bar: 10 µm. c: Scheme of the experimental procedure. PNFLX protocol was followed by patch-clamp recordings in acute brain slices obtained from adult mice. d: Representative current-clamp traces showing the response to 0.8 s-long current injections from SERT+ and SERT- PNs. Red and orange traces: SERT+ PNs in CTR and PNFLX, respectively. Black and gray traces: SERT- PNs in CTR and PNFLX, respectively. current injections: from -100 to +375 pA in all cases. e: Firing rate vs. current injections in all cases. Same colors as in D. *P < 0.05; **P < 0.01; ***P < 0.001. f: Scheme of the experimental procedure. Same as in C, except that during PNFLX protocol mice received concomitant intraperitoneal injections of saline solution or saline solution containing the 5-HT7 antagonist (SB269970) twice a day. g-h: Same as in d-e but in the presence of SB269970 (SB).
Sert Cre Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jackson Laboratory sert fl/fl ; emx1-cre mice
a: Confocal fluorescence micrograph illustrating a section of the PFC of a <t>SERT-Cre::tdTomato</t> adult mouse. Note the dense labeling of deep-layer tdTomato-positive neurons. Scale bar: 500 µm b: Close-up of the micrograph of A showing deep-layer, fluorescent SERT+ cells and shadows of SERT- cells (asterisks). Scale bar: 10 µm. c: Scheme of the experimental procedure. PNFLX protocol was followed by patch-clamp recordings in acute brain slices obtained from adult mice. d: Representative current-clamp traces showing the response to 0.8 s-long current injections from SERT+ and SERT- PNs. Red and orange traces: SERT+ PNs in CTR and PNFLX, respectively. Black and gray traces: SERT- PNs in CTR and PNFLX, respectively. current injections: from -100 to +375 pA in all cases. e: Firing rate vs. current injections in all cases. Same colors as in D. *P < 0.05; **P < 0.01; ***P < 0.001. f: Scheme of the experimental procedure. Same as in C, except that during PNFLX protocol mice received concomitant intraperitoneal injections of saline solution or saline solution containing the 5-HT7 antagonist (SB269970) twice a day. g-h: Same as in d-e but in the presence of SB269970 (SB).
Sert Fl/Fl ; Emx1 Cre Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


a: Confocal fluorescence micrograph illustrating a section of the PFC of a SERT-Cre::tdTomato adult mouse. Note the dense labeling of deep-layer tdTomato-positive neurons. Scale bar: 500 µm b: Close-up of the micrograph of A showing deep-layer, fluorescent SERT+ cells and shadows of SERT- cells (asterisks). Scale bar: 10 µm. c: Scheme of the experimental procedure. PNFLX protocol was followed by patch-clamp recordings in acute brain slices obtained from adult mice. d: Representative current-clamp traces showing the response to 0.8 s-long current injections from SERT+ and SERT- PNs. Red and orange traces: SERT+ PNs in CTR and PNFLX, respectively. Black and gray traces: SERT- PNs in CTR and PNFLX, respectively. current injections: from -100 to +375 pA in all cases. e: Firing rate vs. current injections in all cases. Same colors as in D. *P < 0.05; **P < 0.01; ***P < 0.001. f: Scheme of the experimental procedure. Same as in C, except that during PNFLX protocol mice received concomitant intraperitoneal injections of saline solution or saline solution containing the 5-HT7 antagonist (SB269970) twice a day. g-h: Same as in d-e but in the presence of SB269970 (SB).

Journal: bioRxiv

Article Title: Alterations of adult prefrontal circuits induced by early postnatal fluoxetine treatment mediated by 5-HT7 receptors

doi: 10.1101/2023.11.30.569458

Figure Lengend Snippet: a: Confocal fluorescence micrograph illustrating a section of the PFC of a SERT-Cre::tdTomato adult mouse. Note the dense labeling of deep-layer tdTomato-positive neurons. Scale bar: 500 µm b: Close-up of the micrograph of A showing deep-layer, fluorescent SERT+ cells and shadows of SERT- cells (asterisks). Scale bar: 10 µm. c: Scheme of the experimental procedure. PNFLX protocol was followed by patch-clamp recordings in acute brain slices obtained from adult mice. d: Representative current-clamp traces showing the response to 0.8 s-long current injections from SERT+ and SERT- PNs. Red and orange traces: SERT+ PNs in CTR and PNFLX, respectively. Black and gray traces: SERT- PNs in CTR and PNFLX, respectively. current injections: from -100 to +375 pA in all cases. e: Firing rate vs. current injections in all cases. Same colors as in D. *P < 0.05; **P < 0.01; ***P < 0.001. f: Scheme of the experimental procedure. Same as in C, except that during PNFLX protocol mice received concomitant intraperitoneal injections of saline solution or saline solution containing the 5-HT7 antagonist (SB269970) twice a day. g-h: Same as in d-e but in the presence of SB269970 (SB).

Article Snippet: In order to record SERT+ pyramidal neurons we crossed B6.129(Cg)- Slc6a4 tm1(cre)Xz /J (Sert-Cre) mice with B6.Cg-Gt(ROSA)26Sor/J mice (td-Tomato) (The Jackson Laboratory, Bar Harbor).

Techniques: Fluorescence, Labeling, Patch Clamp, Saline

a-b: Fluorescent micrographs showing a SERT+ (left) and a SERT- (right) PN filled with biocytin and counterstained with green, fluorescent streptavidin. Neurons were filled in a SERT-Cre::TdTomato mouse. Red fluorescence indicates SERT+ PNs. Scale bar 50 µm. c: Representative somatodendritic reconstructions of biocytin-filled SERT+ and SERT- PNs in CTR and PNFLX. Scale bar 100 µm. d: Number of intersections plotted as a function of the distance from soma for basal (lef) and apical (right) dendrites for the two cell types (SERT+ and SERT-), for both treatments (CTR and PNFLX). The yellow box corresponds to the data points that are significantly different between SERT+ and SERT- PNs (* : P<0.005).

Journal: bioRxiv

Article Title: Alterations of adult prefrontal circuits induced by early postnatal fluoxetine treatment mediated by 5-HT7 receptors

doi: 10.1101/2023.11.30.569458

Figure Lengend Snippet: a-b: Fluorescent micrographs showing a SERT+ (left) and a SERT- (right) PN filled with biocytin and counterstained with green, fluorescent streptavidin. Neurons were filled in a SERT-Cre::TdTomato mouse. Red fluorescence indicates SERT+ PNs. Scale bar 50 µm. c: Representative somatodendritic reconstructions of biocytin-filled SERT+ and SERT- PNs in CTR and PNFLX. Scale bar 100 µm. d: Number of intersections plotted as a function of the distance from soma for basal (lef) and apical (right) dendrites for the two cell types (SERT+ and SERT-), for both treatments (CTR and PNFLX). The yellow box corresponds to the data points that are significantly different between SERT+ and SERT- PNs (* : P<0.005).

Article Snippet: In order to record SERT+ pyramidal neurons we crossed B6.129(Cg)- Slc6a4 tm1(cre)Xz /J (Sert-Cre) mice with B6.Cg-Gt(ROSA)26Sor/J mice (td-Tomato) (The Jackson Laboratory, Bar Harbor).

Techniques: Fluorescence

a: Representative voltage-clamp traces of glutamatergic sEPSCs recorded from PFC PNs of adult CTR and PNFLX-treated mice. b: Population data of sEPSC frequency (left) and amplitude (right) in SERT+ and SERT- PNs in CTR and PNFLX-treated mice. Green and black lines indicate median and mean values. resepctively. c-d: Same as in a-b but for GABAergic sIPSCS, isolated using a high-chloride intracellular solution and in the continuous presence of ionotropic glutamate receptor antagonists in the extracellular superfusate

Journal: bioRxiv

Article Title: Alterations of adult prefrontal circuits induced by early postnatal fluoxetine treatment mediated by 5-HT7 receptors

doi: 10.1101/2023.11.30.569458

Figure Lengend Snippet: a: Representative voltage-clamp traces of glutamatergic sEPSCs recorded from PFC PNs of adult CTR and PNFLX-treated mice. b: Population data of sEPSC frequency (left) and amplitude (right) in SERT+ and SERT- PNs in CTR and PNFLX-treated mice. Green and black lines indicate median and mean values. resepctively. c-d: Same as in a-b but for GABAergic sIPSCS, isolated using a high-chloride intracellular solution and in the continuous presence of ionotropic glutamate receptor antagonists in the extracellular superfusate

Article Snippet: In order to record SERT+ pyramidal neurons we crossed B6.129(Cg)- Slc6a4 tm1(cre)Xz /J (Sert-Cre) mice with B6.Cg-Gt(ROSA)26Sor/J mice (td-Tomato) (The Jackson Laboratory, Bar Harbor).

Techniques: Isolation