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Noldus Information Technology phenotyper home cages
Phenotyper Home Cages, supplied by Noldus Information Technology, 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/phenotyper+home+cages/noldus+phenotyper/pm42092139-565-11-14
Average 86 stars, based on 1 article reviews
phenotyper home cages - by Bioz Stars, 2026-09
86/100 stars

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Article Title: UTE MRI for Assessing Demyelination in an mTBI Mouse Model: An Open-field Low-intensity Blast Study
Article Snippet: Spontaneous behaviors were assessed in sham controls and mTBI mice using the PhenoTyper home cages (Model 3000; Noldus Information Technology, Wageningen, The Netherlands), as previously described 39 – 41 .

Article Title: WWC1 mutation drives dopamine dysregulation and synaptic imbalance in Tourette's syndrome.
Article Snippet: To assess the natural exploratory motivation and repetitive behaviors of mice, individual testing was conducted with video recording in the PhenoTyper home cages (40 cm by 40 cm by 40 cm, Noldus, Holland), which provided a home- like environment for mice, complete with ample food and water supply.

Article Title: WWC1 mutation drives dopamine dysregulation and synaptic imbalance in Tourette’s syndrome
Article Snippet: To assess the natural exploratory motivation and repetitive behaviors of mice, individual testing was conducted with video recording in the PhenoTyper home cages (40 cm by 40 cm by 40 cm, Noldus, Holland), which provided a home-like environment for mice, complete with ample food and water supply.

Article Title: Allosteric activation of a cell-type-specific GPR120 inhibits amyloid pathology of Alzheimer’s disease
Article Snippet: Natural exploratory motivation and repetitive behaviors were assessed in PhenoTyper home cages (40 cm × 40 cm × 40 cm, Noldus) under controlled light (12 h/12 h) and temperature conditions.

Article Title: Allosteric activation of a cell-type-specific GPR120 inhibits amyloid pathology of Alzheimer's disease.
Article Snippet: Natural exploratory motivation and repetitive behaviors were assessed in PhenoTyper home cages (40 cm × 40 cm × 40 cm, Noldus) under controlled light (12 h/12 h) and temperature conditions.

Article Title: Cell‐Type Specific Circuits in the Mammillary Body for Place and Object Recognition Memory
Article Snippet: To evaluate natural exploratory motivation and repetitive behaviors, individual mice were video‐recorded alone in the PhenoTyper home cages (40 × 40 × 40 cm, Noldus, Holland) which provided a home environment for mice, with sufficient food and water supply.

Article Title: A cell-type–specific epigenetic mechanism encodes social investigatory behavior via Lrhcn1 and Hcn1
Article Snippet: To examine natural investigatory behavior, three male mice from the same littermates were video recorded in the PhenoTyper home cages (40 cm by 40 cm by 40 cm, Noldus, Holland), equipped with a home environment including sufficiency food and water supply at 10 a.m. in a 12-hour/12-hour light/dark-cycled and air-controlled room.

Mouse Assay:

Article Title: A brain reward circuit inhibited by next-generation weight-loss drugs in mice.
Article Snippet: .. Home-cage monitoring of Glp1rS33W mice Mice were single-housed and acclimatized to PhenoTyper home cages (Noldus) for 5 days before testing. ..



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TSE systems automated home cage phenotyping system
(A) Schemata (created with BioRender.com ) to map activity-dependent Fos expression in mice fed a HFD for 7 days. Right panel: coronal views of the p-value of the voxel maps for Fos-positive cell densities at two different levels of DRN. White arrows indicate DRN regions significantly activated after 7 days of HFD feeding. ABA (Allen Brain Atlas) annotated image. (B) Time-course quantification of cFOS-positive neurons in the DRN of mice fed an HFD for 3 days, 2 weeks, and 16 weeks and representative immunohistochemical staining of cFOS in the DRN of mice fed an HFD for 16 weeks. (scale bar = 100um) (C) Schemata for chemogenetic inhibition of DRN VGAT neurons in vGat-IRES-Cre mice injected with CNO twice a day for 11 weeks in the preventive approach or injected daily for 17 days in DIO mice for the curative approach (right). Body weight change in mice fed a HFD for 11 weeks along with DRN VGAT neurons chemogenetic inhibition (n= 6-7 per group, P <0.0001) (middle) and body weight of DIO mice before and after chemogenetic inhibition of DRN VGAT neurons for 17 days (right) (n= 6-7 per group, P <0.0001). (D-G) (n= 6-7 per group, P < 0.05), Metabolic <t>phenotyping</t> of vGat-IRES-Cre after completion of the preventive approach. (D) Adiposity (% total body weight) (E) Average food intake (F) Interscapular BAT temperature (G) Whole-body median temperature (H-K) Indirect calorimetry of DIO Vgat-IRES-Cre mice injected inhibitory DREADDs and placed in metabolic cages for measurement of (H) oxygen consumption (VO 2 ), oxygen dioxide production (VCO 2 ), (J) locomotion activity and (K) energy expenditure. Data are represented as mean ± s.e.m. P values were calculated using a or an unpaired two-tailed Student’s t -test ( A, D-G ), two-way ANOVA with a multiple-comparisons test using a Tukey post-hoc approach ( C ) or using CalR software and a two-sided ANCOVA regression analysis taking body weight into account ( H-K ). P < 0.05 is considered significant. The CNO dose used was 1 mg/kg.
Automated Home Cage Phenotyping System, supplied by TSE systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phenotyper+home+cages/automated+home+cage+phenotyping+system/bio_rxiv__2025__04__24__650283-205-25-29
Average 90 stars, based on 1 article reviews
automated home cage phenotyping system - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

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(A) Schemata (created with BioRender.com ) to map activity-dependent Fos expression in mice fed a HFD for 7 days. Right panel: coronal views of the p-value of the voxel maps for Fos-positive cell densities at two different levels of DRN. White arrows indicate DRN regions significantly activated after 7 days of HFD feeding. ABA (Allen Brain Atlas) annotated image. (B) Time-course quantification of cFOS-positive neurons in the DRN of mice fed an HFD for 3 days, 2 weeks, and 16 weeks and representative immunohistochemical staining of cFOS in the DRN of mice fed an HFD for 16 weeks. (scale bar = 100um) (C) Schemata for chemogenetic inhibition of DRN VGAT neurons in vGat-IRES-Cre mice injected with CNO twice a day for 11 weeks in the preventive approach or injected daily for 17 days in DIO mice for the curative approach (right). Body weight change in mice fed a HFD for 11 weeks along with DRN VGAT neurons chemogenetic inhibition (n= 6-7 per group, P <0.0001) (middle) and body weight of DIO mice before and after chemogenetic inhibition of DRN VGAT neurons for 17 days (right) (n= 6-7 per group, P <0.0001). (D-G) (n= 6-7 per group, P < 0.05), Metabolic phenotyping of vGat-IRES-Cre after completion of the preventive approach. (D) Adiposity (% total body weight) (E) Average food intake (F) Interscapular BAT temperature (G) Whole-body median temperature (H-K) Indirect calorimetry of DIO Vgat-IRES-Cre mice injected inhibitory DREADDs and placed in metabolic cages for measurement of (H) oxygen consumption (VO 2 ), oxygen dioxide production (VCO 2 ), (J) locomotion activity and (K) energy expenditure. Data are represented as mean ± s.e.m. P values were calculated using a or an unpaired two-tailed Student’s t -test ( A, D-G ), two-way ANOVA with a multiple-comparisons test using a Tukey post-hoc approach ( C ) or using CalR software and a two-sided ANCOVA regression analysis taking body weight into account ( H-K ). P < 0.05 is considered significant. The CNO dose used was 1 mg/kg.

Journal: bioRxiv

Article Title: Identification of a Thermogenic Target in the Dorsal Raphe Nucleus for Weight Management

doi: 10.1101/2025.04.24.650283

Figure Lengend Snippet: (A) Schemata (created with BioRender.com ) to map activity-dependent Fos expression in mice fed a HFD for 7 days. Right panel: coronal views of the p-value of the voxel maps for Fos-positive cell densities at two different levels of DRN. White arrows indicate DRN regions significantly activated after 7 days of HFD feeding. ABA (Allen Brain Atlas) annotated image. (B) Time-course quantification of cFOS-positive neurons in the DRN of mice fed an HFD for 3 days, 2 weeks, and 16 weeks and representative immunohistochemical staining of cFOS in the DRN of mice fed an HFD for 16 weeks. (scale bar = 100um) (C) Schemata for chemogenetic inhibition of DRN VGAT neurons in vGat-IRES-Cre mice injected with CNO twice a day for 11 weeks in the preventive approach or injected daily for 17 days in DIO mice for the curative approach (right). Body weight change in mice fed a HFD for 11 weeks along with DRN VGAT neurons chemogenetic inhibition (n= 6-7 per group, P <0.0001) (middle) and body weight of DIO mice before and after chemogenetic inhibition of DRN VGAT neurons for 17 days (right) (n= 6-7 per group, P <0.0001). (D-G) (n= 6-7 per group, P < 0.05), Metabolic phenotyping of vGat-IRES-Cre after completion of the preventive approach. (D) Adiposity (% total body weight) (E) Average food intake (F) Interscapular BAT temperature (G) Whole-body median temperature (H-K) Indirect calorimetry of DIO Vgat-IRES-Cre mice injected inhibitory DREADDs and placed in metabolic cages for measurement of (H) oxygen consumption (VO 2 ), oxygen dioxide production (VCO 2 ), (J) locomotion activity and (K) energy expenditure. Data are represented as mean ± s.e.m. P values were calculated using a or an unpaired two-tailed Student’s t -test ( A, D-G ), two-way ANOVA with a multiple-comparisons test using a Tukey post-hoc approach ( C ) or using CalR software and a two-sided ANCOVA regression analysis taking body weight into account ( H-K ). P < 0.05 is considered significant. The CNO dose used was 1 mg/kg.

Article Snippet: Energy expenditure was assessed through measurement by indirect calorimetry of oxygen consumption (VO2), carbon dioxide production (VCO2), heat production, and locomotor activity using an automated home cage phenotyping system (TSE Systems).

Techniques: Activity Assay, Expressing, Immunohistochemical staining, Staining, Inhibition, Injection, Two Tailed Test, Software