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Med Associates Inc videofreezetm video fear conditioning program
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Male or female wild-type mice ( Taar5 +/+ ) or mice lacking the TMA receptor ( Taar5 -/ ) were subjected to a battery of behavioral tests related to cognition, depression, and anxiety including: ( A ) cued fear <t>conditioning,</t> ( B ) elevated plus maze, ( C ) Y-maze, and ( D ) open field test as described in the Methods section. Data are shown for the entire cohort combining both sexes or divided into either male or female cohorts to examine sexual dimorphism in phenotype. Data represent the mean ± SEM from n = 9–10 per group when male and female are separated ( n = 19–20 when both sexes are combined). Significant differences between Taar5 +/+ and Taar5 -/- mice were determined by Student’s t -tests (*p < 0.05).
Fear Conditioning Chambers, supplied by Med Associates Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Male or female wild-type mice ( Taar5 +/+ ) or mice lacking the TMA receptor ( Taar5 -/ ) were subjected to a battery of behavioral tests related to cognition, depression, and anxiety including: ( A ) cued fear <t>conditioning,</t> ( B ) elevated plus maze, ( C ) Y-maze, and ( D ) open field test as described in the Methods section. Data are shown for the entire cohort combining both sexes or divided into either male or female cohorts to examine sexual dimorphism in phenotype. Data represent the mean ± SEM from n = 9–10 per group when male and female are separated ( n = 19–20 when both sexes are combined). Significant differences between Taar5 +/+ and Taar5 -/- mice were determined by Student’s t -tests (*p < 0.05).
Fear Conditioning Tests, supplied by Med Associates Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Male or female wild-type mice ( Taar5 +/+ ) or mice lacking the TMA receptor ( Taar5 -/ ) were subjected to a battery of behavioral tests related to cognition, depression, and anxiety including: ( A ) cued fear <t>conditioning,</t> ( B ) elevated plus maze, ( C ) Y-maze, and ( D ) open field test as described in the Methods section. Data are shown for the entire cohort combining both sexes or divided into either male or female cohorts to examine sexual dimorphism in phenotype. Data represent the mean ± SEM from n = 9–10 per group when male and female are separated ( n = 19–20 when both sexes are combined). Significant differences between Taar5 +/+ and Taar5 -/- mice were determined by Student’s t -tests (*p < 0.05).
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Med Associates Inc auditory fear conditioning
CnF-LA/B pathway instructs aversive memory formation. a ) Fear <t>conditioning</t> paradigm with laser inhibition during the peri-shock period (top) and viral/optogenetic strategy (bottom). b ) Optogenetic inactivation of CnF-LA/B projecting cell bodies reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 16) = 14.61, P =0.0002). c ) Optogenetic inhibition of CnF terminals in LA/B viral/optogenetic approach (top) and fluorophore labeled CnF terminals in LA/B (bottom). d ) Optogenetic inactivation of CnF terminals in LA/B reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 21) = 24.34, P <0.0001). e ) Conditioning paradigm for tone-laser stimulation of Cnf-LA/B pathway (top) viral/optogenetic strategy (bottom). f ) Pairing tone with optogenetic stimulation of CnF-LA/B pathway produces fear learning during the acquisition session (two-way ANOVA, F (2, 144) = 76.64, P <0.0001). Single trials on y-axis. g ) Increased conditioned freezing is maintained in ChR2 paired group at memory retrieval (one-way ANOVA, F (2, 18) = 8.471, P =0.0026). h ) Effect of optogenetic inhibition of CnF-to-LA/B pathway on escape behaviors. i ) Interpretative working model showing CnF-to-LA pathway receiving inputs from brain regions involved in aversive sensory processing and hierarchically organized defensive responding and, in turn, sending external-sensory and internal-motor information to LA/B to instruct associative emotional memory formation and enhance escape responding. ** P <0.01, *** P <0.001. Data represent mean ± SEM
Auditory Fear Conditioning, supplied by Med Associates Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Med Associates Inc conditioning chamber
CnF-LA/B pathway instructs aversive memory formation. a ) Fear <t>conditioning</t> paradigm with laser inhibition during the peri-shock period (top) and viral/optogenetic strategy (bottom). b ) Optogenetic inactivation of CnF-LA/B projecting cell bodies reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 16) = 14.61, P =0.0002). c ) Optogenetic inhibition of CnF terminals in LA/B viral/optogenetic approach (top) and fluorophore labeled CnF terminals in LA/B (bottom). d ) Optogenetic inactivation of CnF terminals in LA/B reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 21) = 24.34, P <0.0001). e ) Conditioning paradigm for tone-laser stimulation of Cnf-LA/B pathway (top) viral/optogenetic strategy (bottom). f ) Pairing tone with optogenetic stimulation of CnF-LA/B pathway produces fear learning during the acquisition session (two-way ANOVA, F (2, 144) = 76.64, P <0.0001). Single trials on y-axis. g ) Increased conditioned freezing is maintained in ChR2 paired group at memory retrieval (one-way ANOVA, F (2, 18) = 8.471, P =0.0026). h ) Effect of optogenetic inhibition of CnF-to-LA/B pathway on escape behaviors. i ) Interpretative working model showing CnF-to-LA pathway receiving inputs from brain regions involved in aversive sensory processing and hierarchically organized defensive responding and, in turn, sending external-sensory and internal-motor information to LA/B to instruct associative emotional memory formation and enhance escape responding. ** P <0.01, *** P <0.001. Data represent mean ± SEM
Conditioning Chamber, supplied by Med Associates Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/conditioning chamber/product/Med Associates Inc
Average 96 stars, based on 1 article reviews
conditioning chamber - by Bioz Stars, 2026-03
96/100 stars
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Male or female wild-type mice ( Taar5 +/+ ) or mice lacking the TMA receptor ( Taar5 -/ ) were subjected to a battery of behavioral tests related to cognition, depression, and anxiety including: ( A ) cued fear conditioning, ( B ) elevated plus maze, ( C ) Y-maze, and ( D ) open field test as described in the Methods section. Data are shown for the entire cohort combining both sexes or divided into either male or female cohorts to examine sexual dimorphism in phenotype. Data represent the mean ± SEM from n = 9–10 per group when male and female are separated ( n = 19–20 when both sexes are combined). Significant differences between Taar5 +/+ and Taar5 -/- mice were determined by Student’s t -tests (*p < 0.05).

Journal: eLife

Article Title: Gut microbe-derived trimethylamine shapes circadian rhythms through the host receptor TAAR5

doi: 10.7554/eLife.107037

Figure Lengend Snippet: Male or female wild-type mice ( Taar5 +/+ ) or mice lacking the TMA receptor ( Taar5 -/ ) were subjected to a battery of behavioral tests related to cognition, depression, and anxiety including: ( A ) cued fear conditioning, ( B ) elevated plus maze, ( C ) Y-maze, and ( D ) open field test as described in the Methods section. Data are shown for the entire cohort combining both sexes or divided into either male or female cohorts to examine sexual dimorphism in phenotype. Data represent the mean ± SEM from n = 9–10 per group when male and female are separated ( n = 19–20 when both sexes are combined). Significant differences between Taar5 +/+ and Taar5 -/- mice were determined by Student’s t -tests (*p < 0.05).

Article Snippet: Other , Fear Conditioning Chambers , Med Associates , #VFC-008 , Behavioral testing.

Techniques: Battery

CnF-LA/B pathway instructs aversive memory formation. a ) Fear conditioning paradigm with laser inhibition during the peri-shock period (top) and viral/optogenetic strategy (bottom). b ) Optogenetic inactivation of CnF-LA/B projecting cell bodies reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 16) = 14.61, P =0.0002). c ) Optogenetic inhibition of CnF terminals in LA/B viral/optogenetic approach (top) and fluorophore labeled CnF terminals in LA/B (bottom). d ) Optogenetic inactivation of CnF terminals in LA/B reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 21) = 24.34, P <0.0001). e ) Conditioning paradigm for tone-laser stimulation of Cnf-LA/B pathway (top) viral/optogenetic strategy (bottom). f ) Pairing tone with optogenetic stimulation of CnF-LA/B pathway produces fear learning during the acquisition session (two-way ANOVA, F (2, 144) = 76.64, P <0.0001). Single trials on y-axis. g ) Increased conditioned freezing is maintained in ChR2 paired group at memory retrieval (one-way ANOVA, F (2, 18) = 8.471, P =0.0026). h ) Effect of optogenetic inhibition of CnF-to-LA/B pathway on escape behaviors. i ) Interpretative working model showing CnF-to-LA pathway receiving inputs from brain regions involved in aversive sensory processing and hierarchically organized defensive responding and, in turn, sending external-sensory and internal-motor information to LA/B to instruct associative emotional memory formation and enhance escape responding. ** P <0.01, *** P <0.001. Data represent mean ± SEM

Journal: bioRxiv

Article Title: A sensorimotor brain circuit for transforming aversive experiences into emotional states

doi: 10.64898/2026.01.15.699823

Figure Lengend Snippet: CnF-LA/B pathway instructs aversive memory formation. a ) Fear conditioning paradigm with laser inhibition during the peri-shock period (top) and viral/optogenetic strategy (bottom). b ) Optogenetic inactivation of CnF-LA/B projecting cell bodies reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 16) = 14.61, P =0.0002). c ) Optogenetic inhibition of CnF terminals in LA/B viral/optogenetic approach (top) and fluorophore labeled CnF terminals in LA/B (bottom). d ) Optogenetic inactivation of CnF terminals in LA/B reduces auditory fear memory formation. Top, acquisition. Bottom, memory retrieval (one-way ANOVA, F (2, 21) = 24.34, P <0.0001). e ) Conditioning paradigm for tone-laser stimulation of Cnf-LA/B pathway (top) viral/optogenetic strategy (bottom). f ) Pairing tone with optogenetic stimulation of CnF-LA/B pathway produces fear learning during the acquisition session (two-way ANOVA, F (2, 144) = 76.64, P <0.0001). Single trials on y-axis. g ) Increased conditioned freezing is maintained in ChR2 paired group at memory retrieval (one-way ANOVA, F (2, 18) = 8.471, P =0.0026). h ) Effect of optogenetic inhibition of CnF-to-LA/B pathway on escape behaviors. i ) Interpretative working model showing CnF-to-LA pathway receiving inputs from brain regions involved in aversive sensory processing and hierarchically organized defensive responding and, in turn, sending external-sensory and internal-motor information to LA/B to instruct associative emotional memory formation and enhance escape responding. ** P <0.01, *** P <0.001. Data represent mean ± SEM

Article Snippet: For all auditory fear conditioning in behavioral studies, animals were placed into a sound-isolating chamber (Med Associates) and received auditory CSs (74 dB, 5-kHz tone pips at 1 Hz with 250 ms on and 750 ms off for 20 s) and electric shock unconditioned stimuli (US) (1 sec, 0.7mA) which co-terminated with the CS.

Techniques: Inhibition, Labeling