This productRodent standard
T Maze Apparatus
Start arm with two goal arms, removable doors, and optional reward wells
General-purpose T Maze for alternation, forced-choice, and reward-discrimination protocols in mice or rats.
Quote
Request Quote
1 / 4
T Maze
SKU 3401/2/3
In Stock — ships now$1,790.00
IncludesStandard care
Classic T-shaped behavioral maze for assessing spatial learning, working memory, and choice behavior in mice and rats through spontaneous alternation and discrimination learning paradigms.
CE MarkedBAA available
Scientist guidance
Louise Corscadden, PhD
Director of Science · ConductScience
Ask Louise about T Maze fit, setup, configuration, or quote prep.
Already working with us? Sign in to connect this with My Scientist.
Key Specifications
Full details →- Model fit
- 5 selectable configurations
- SKU family
- 3401/2/3
- Sizing
- 117.0 x 66.0 x 10.0 cm
- Ordering
- Online checkout and quote request available
- Category
- Behavioral Mazes
- Build notes
- Confirm accessories, station layout, and support needs before purchase
The T-Maze is a fundamental behavioral testing apparatus designed for assessing spatial learning, working memory, and decision-making processes in rodents. This classic maze configuration consists of a central stem leading to two perpendicular arms, creating the characteristic T-shape that allows researchers to evaluate spontaneous alternation behavior, delayed alternation tasks, and choice discrimination learning.
Constructed from odor-free acrylic with clean ethanol compatibility, the apparatus is available in three size configurations optimized for different rodent species. The maze supports multiple experimental paradigms including spatial navigation testing, reward-based learning protocols, and memory assessment tasks commonly employed in neurobehavioral research and cognitive phenotyping studies.
How It Works
The T-Maze operates on the principle of spatial choice behavior, exploiting rodents' natural tendency for spontaneous alternation. In the most basic paradigm, animals are placed in the stem of the maze and allowed to choose between the two arms. Normal rodents exhibit approximately 60-80% alternation behavior, meaning they tend to enter the arm opposite to their previous choice on successive trials.
The maze can be configured for multiple experimental paradigms. In delayed alternation tasks, animals are first forced into one arm, then after a delay period, given free access to both arms. Working memory is assessed by measuring the animal's ability to remember the previously visited arm and choose the alternate arm. Reward-based protocols place food or water reinforcement in specific arms to assess learning acquisition and retention.
Data collection typically involves recording arm entry sequences, latency to make choices, and time spent in each arm. The apparatus supports both manual observation and automated tracking when integrated with video monitoring systems or photobeam detection arrays.
Features & Benefits
Three size configurations (Mouse small, Mouse, Rat)
Accommodates different rodent species with appropriate spatial scaling for natural movement and choice behavior expression.
Odor-free acrylic construction
Prevents olfactory cues from influencing choice behavior, ensuring spatial and cognitive factors drive decision-making.
70% ethanol compatible surfaces
Enables rapid inter-trial cleaning to eliminate scent trails while maintaining material integrity over repeated use.
Optional central partition modification
Creates confined start area for controlled trial initiation and prevents premature arm exploration during setup.
Available guillotine door system
Enables precise temporal control over arm access for delayed alternation and forced choice paradigms.
Modular food well integration
Supports reward-based learning protocols with standardized reinforcement delivery locations.
Multiple maze variation compatibility
Expandable to elevated, water-based, or multi-unit configurations for diverse experimental approaches.
Standardized arm dimensions
Ensures reproducible spatial relationships across studies and facilitates comparison with published literature protocols.
Weight
- 15.0 kg
Dimensions
- L: 117.0 mm
- W: 66.0 mm
- H: 10.0 mm
| Feature | This Product | Typical Alternative | Advantage |
|---|---|---|---|
| Species Size Options | Three distinct size configurations (Mouse small, Mouse, Rat) with species-appropriate scaling | Many models offer single-size construction requiring adaptation for different species | Ensures optimal spatial scaling for natural movement patterns and choice behavior expression across rodent species. |
| Modification Compatibility | Extensive modification options including food wells, doors, light cues, backlights, and housing systems | Basic models often have limited modification capabilities | Enables protocol adaptation for diverse experimental paradigms without requiring multiple apparatus purchases. |
| Construction Material | Odor-free acrylic with 70% ethanol compatibility and optical clarity | Some alternatives use wood, metal, or lower-grade plastics with potential odor retention | Prevents olfactory cueing while enabling visual observation and maintaining chemical resistance for repeated cleaning cycles. |
| Arm Configuration Options | Multiple arm configurations from enclosed start with open goals to fully enclosed designs | Fixed configuration models limit experimental flexibility | Supports diverse behavioral paradigms from anxiety-related elevated protocols to controlled spatial memory assessment. |
| Central Partition System | Optional central partition with 10 cm corridor width modification | Many designs lack controlled start area options | Provides precise trial initiation control and prevents premature exploration during experimental setup phases. |
The T-Maze distinguishes itself through comprehensive size scaling across rodent species, extensive modification compatibility, and specialized features for controlled behavioral assessment. The acrylic construction and optional partition systems support both basic alternation protocols and complex temporal discrimination paradigms.
| Model | SKU | Listed price | Status | Dimensions |
|---|---|---|---|---|
| Rat | 3401/2/3 | $1,790.00 | Available | 117.0 x 66.0 x 10.0 cm |
| Mouse | 3401/2/3 | $1,290.00 | Available | 117.0 x 66.0 x 10.0 cm |
| Mouse Small | 3401/2/3 | $1,190.00 | Available | 117.0 x 66.0 x 10.0 cm |
| Product model | 3401/2/3 | $1,390.00 | Available | 117.0 x 66.0 x 10.0 cm |
| Mouse (small) | ME-3403 | $1,190.00 | Available | 30 x 6 x 30 cm |
Neuroscience
Evaluating hippocampus-dependent spatial working memory through spontaneous alternation tasks where rodents naturally alternate arm choices between consecutive trials.
Behavioral Pharmacology
Assessing cognitive effects of pharmaceutical compounds by measuring changes in alternation behavior and choice accuracy before and after drug administration.
Learning and Memory
Conducting delayed alternation experiments to measure working memory span by imposing varying delay intervals between forced and free choice trials.
Neurodegeneration
Monitoring cognitive decline progression in disease models by tracking deterioration in spontaneous alternation performance and spatial navigation accuracy.
Addiction Research
Investigating decision-making alterations in substance dependence models through reward-based choice paradigms and preference testing protocols.
Aging Research
Comparing spatial memory performance between young and aged cohorts to identify age-related cognitive changes and intervention effects.
Practical Tips
Calibration
Validate spontaneous alternation rates with control subjects before experimental use, targeting 60-80% alternation in healthy animals.
Why: Baseline validation ensures apparatus configuration produces expected behavioral responses before introducing experimental variables.
Maintenance
Inspect acrylic panels weekly for stress cracks or scratches that could create visual artifacts or compromise structural integrity.
Why: Early detection prevents apparatus failure during experiments and maintains consistent visual conditions across testing sessions.
Best Practices
Maintain consistent environmental lighting and minimize external visual cues that could bias arm choice selection.
Why: Spatial choice behavior should reflect internal navigation processes rather than external environmental asymmetries.
Troubleshooting
If alternation rates consistently fall below 50%, evaluate for systematic biases such as lighting gradients, odor trails, or apparatus positioning.
Why: Below-chance performance typically indicates environmental factors overwhelming natural alternation tendencies rather than cognitive impairment.
Data Quality
Record arm entry sequences, choice latencies, and time spent in each zone to capture comprehensive behavioral profiles beyond simple choice measures.
Why: Additional parameters provide insight into decision confidence, exploration patterns, and potential anxiety-related factors affecting choice behavior.
Safety
Allow complete ethanol evaporation between cleaning and animal placement to prevent respiratory irritation and behavioral artifacts.
Why: Residual ethanol vapors can cause avoidance behaviors and stress responses that confound spatial choice measurements.
Best Practices
Implement counterbalanced apparatus orientation across subjects to control for potential directional biases in the testing environment.
Why: Systematic rotation helps distinguish genuine spatial memory effects from environmental asymmetries that could influence arm preferences.
Data Quality
Establish clear arm entry criteria (e.g., all four paws past arm threshold) and apply consistently across all trials and subjects.
Why: Standardized entry definitions prevent scoring variability and ensure reliable measurement of choice behavior across experimental sessions.
Setup Guide
Unpack and Inspect
Remove maze components from packaging and inspect acrylic panels for damage or stress cracks that could affect structural integrity.
Assembly Configuration
Assemble the T-maze according to species requirements, ensuring proper alignment of stem and arm sections with secure panel connections.
Optional Modifications
Install any requested modifications such as food wells, guillotine doors, or central partitions according to experimental protocol requirements.
Surface Preparation
Clean all surfaces with 70% ethanol and allow complete drying to eliminate residual odors that could influence animal behavior.
Environmental Setup
Position maze in testing room with consistent lighting and minimal external visual cues that could bias arm choice behavior.
Baseline Validation
Conduct preliminary testing with control animals to verify spontaneous alternation rates fall within expected ranges before experimental use.
Protocol Implementation
Begin experimental sessions following established habituation periods and inter-trial cleaning protocols to maintain consistent testing conditions.
What’s in the Box
- T-Maze apparatus (assembled or flat-pack depending on configuration)
- Acrylic wall panels and base sections
- Assembly hardware and connection elements (typical)
- Cleaning and maintenance instructions (typical)
- Protocol reference guide (typical)
Warranty
ConductScience provides a standard one-year manufacturer warranty covering material defects and workmanship issues. Technical support includes protocol consultation and troubleshooting assistance for experimental setup optimization.
Compliance
IACUC GuidelinesCommonly used in animal research protocols subject to institutional animal care and use committee oversight for behavioral testing procedures.
ARRIVE GuidelinesSupports standardized reporting requirements for animal research methodology and experimental design documentation.
Good Laboratory Practice (GLP)Compatible with GLP protocols for behavioral pharmacology studies requiring standardized apparatus and documentation procedures.
References
Background reading relevant to this product:
1.Norberto Cysne Coimbra et al. (2017) “Critical neuropsychobiological analysis of panic attack- and anticipatory anxiety-like behaviors in rodents confronted with snakes in polygonal arenas and complex labyrinths: a comparison to the elevated plus- and T-maze behavioral tests” Brazilian Journal of Psychiatry doi:10.1590/1516-4446-2015-1895
2.Herbert Schwegler et al. (1990) “Hippocampal mossy fibers and radial-maze learning in the mouse: A correlation with spatial working memory but not with non-spatial reference memory” Neuroscience doi:10.1016/0306-4522(90)90139-u
3.Charles V. Vorhees et al. (2006) “Morris water maze: procedures for assessing spatial and related forms of learning and memory” Nature Protocols doi:10.1038/nprot.2006.116
4.Rudi D'Hooge et al. (2001) “Applications of the Morris water maze in the study of learning and memory” Brain Research Reviews doi:10.1016/s0165-0173(01)00067-4
Q
What is the T-Maze?
A
The T-Maze is a simple two-choice behavioral apparatus shaped like the letter T, used to assess spatial memory, learning, and decision-making in rodents through forced-choice alternation tasks.
Q
How does the T-Maze work?
A
Rodents start in the stem of the T and choose between the left or right goal arm. In rewarded alternation, animals learn to alternate choices to receive a food reward. Correct alternation percentage measures working memory performance.
Q
What research applications use the T-Maze?
A
The T-Maze is used in prefrontal cortex research, working memory studies, and reward-based learning paradigms. It is commonly applied in schizophrenia models, ADHD research, and pharmacological studies of cognition.
Have a question about this product?
Ask a question
Have a question? Just ask.
Send it over and we'll email you a personalized answer — no call, no scheduling.
Personalized email reply
Usually within one business day
Helpful answers published here
Prefer to talk it through?
Accessories
Enhance your setup with compatible accessories
Total: $0.00
Frequently Bought Together
+
+
+
+
Total: $3,730.00
Creator Insights
Edward C. TolmanEstablished cognitive-map theory underlying T-maze spatial learning (1948)University of California, Berkeley
About the Creator
Edward Chace Tolman (1886–1959) was an American experimental psychologist and longtime professor at the University of California, Berkeley. He developed purposive behaviorism, which brought cognitive variables — expectancy, purpose and spatial representation — into the study of animal behavior. His 1948 Psychological Review paper, drawn from two decades of maze research, argued that rats form internal cognitive maps rather than rote stimulus-response chains, reframing what maze performance measures. The T-maze apparatus predates Tolman and has no single inventor, but his 1948 synthesis remains the dominant theoretical anchor for spatial-choice and place-learning paradigms in behavioral neuroscience.
To view Edward C. Tolman’s publications, visit PubMed.
Did you work with Edward C. Tolman? to suggest corrections or share material for these Creator Insights.
ConductScience celebrates method creators: researchers who, through rigorous and often ingenious experiments, develop the tools that reveal how the brain and body work. These are real scientific discoveries that become everyday instruments for the labs that follow.
Foundational paper
- Tolman, E. C. (1948). Cognitive maps in rats and men. Psychological Review, 55(4), 189–208. doi:10.1037/h0061626
Use this apparatus with
The complete T Maze workflow
Track choices
Automate left/right choice, decision latency, arm dwell, alternation, and reward-zone timing from overhead video.
ConductVision T Maze ->Run protocol
Spontaneous alternation, rewarded alternation, forced-choice, delayed alternation, and discrimination schedules.
ConductMaze T Maze Protocol ->Calculate choice accuracy
Free calculator for percent correct, alternation rate, side bias, and latency summaries.
T Maze Percent Correct Calculator ->Configuration considerations
Common T Maze setup decisions
Use these notes to scope species, cohort, tracking, and automation needs. Only verified product or support routes are linked from this section.
BuyableMouse format
Mouse T Maze
Scaled arm width, lower wall height, and mouse-sized reward zones
Optimized for mouse alternation, spatial working memory, and high-throughput choice testing.
Quote
View options ->SpecialtyDelay protocols
T Maze With Doors
Manual or automated start and goal-arm doors for forced-choice and delay phases
Best for delayed alternation or forced-sample designs where access timing must be controlled.
Quote
Configure tracking ->§ 1
Introduction
The T Maze is a two-choice apparatus used for spontaneous alternation, rewarded alternation, delayed alternation, and simple discrimination learning. Its value is experimental control: the researcher can reduce a spatial or working-memory question to a left-versus-right choice while still preserving clear apparatus geometry. 1
Spontaneous alternation relies on the natural tendency of rodents to explore a less recently visited arm, while rewarded and delayed alternation add motivation, rule learning, and retention demands. Those variants must be separated in the product page because they require different doors, reward wells, timing, and scoring rules. 1
T Maze data are easy to summarize but easy to overinterpret. Percent correct or alternation rate should be paired with side-bias checks, latency, omissions, forced-trial handling, reward motivation, and arm cleaning so a choice deficit is not mistaken for memory impairment without controls. 1
§ 2
Methods
2.1 Procedure
Two-choice alternation or discrimination testing with pre-defined side-bias and latency controls.
Pre-test setup
- 1.Choose variant: Define spontaneous alternation, rewarded alternation, delayed alternation, or cue/reward discrimination before equipment setup.
- 2.Habituate apparatus: Allow exploration without scoring until animals enter the start arm and both goal arms without excessive freezing or retreating.
- 3.Prepare reward or cue: For rewarded variants, standardize reward type, well position, deprivation schedule, and cleaning between trials.
- 4.Door timing: If doors are used, define forced-run, delay, choice-run, and inter-trial timing before data collection.
Trial sequence
- 1.Start placement: Place the subject in the start arm facing the choice point or according to the protocol-defined orientation.
- 2.Forced or sample phase: In delayed alternation, restrict access to one goal arm, allow the sample visit, then return the animal to the start or holding area.
- 3.Choice phase: Open access to both goal arms and record the first committed arm entry as the choice.1
- 4.Score outcome: Classify alternation, correct rewarded choice, incorrect choice, omission, or correction trial according to the pre-registered rule.
- 5.Reset maze: Clean arms, rebait wells if used, and counterbalance side rules across subjects or sessions.
Critical methodological constraints
- Side bias. A strong left or right preference can look like poor alternation. Report side-bias checks and counterbalancing.
- Motivation. Rewarded variants depend on consistent hunger state, reward preference, and reward visibility.
- Trial definition. Decide whether correction trials count in performance metrics before the experiment starts.
- Delay load. Delayed alternation changes task difficulty. Compare only cohorts tested under the same delay schedule.3
2.2 Measurement & Analysis
Core T Maze endpoints for choice accuracy, alternation, and decision quality.
Percent Correct
Rewarded or rule-based accuracy
Correct choices divided by total valid choice trials.
Alternation Rate
Spontaneous or delayed alternation
Trials in which the animal chooses the opposite goal arm from the previous visit.1
Choice Latency
Decision and motivation
Time from start release to committed goal-arm entry.
Side Bias
Validity control
Imbalance in left versus right choices independent of reward or alternation rule.
Omissions
Task engagement
Trials with no committed choice before the maximum duration.
+ Additional metrics: start latency, goal-arm dwell, correction-trial count, reward retrieval latency, delay-period performance, and within-session learning slope.
2.3 choice accuracy (analysis)
A simple percent-correct index for rewarded or rule-based T Maze protocols.
§ 3
Results
PubMed publication counts, sample apparatus output, and recent papers from a dated PubMed snapshot.
3.1 Publication trends
PubMed volume and co-occurring behavioral methods for T Maze choice and alternation studies.
3.2 Sample apparatus output
Representative output from a rewarded T Maze alternation session.
3.3 Recent findings (PubMed)
- Sep 2026PMID: 42373009
Age- and sex-dependent effects of single prolonged stress on behavioral, hematological, and oxidative stress parameters in C57BL/6J mice.
Balatskyi V, Demianchuk O, Gospodaryov D, et al.. Neuroscience. 2026 Sep 11.
Post-traumatic stress disorder (PTSD) is a pathological condition associated with the experience of traumatic stress.
- Sep 2026PMID: 42760272
Decoding Medial Entorhinal Cortical Dynamics Produces Planning-Like Alternations in Hippocampal theta Sequences.
Nakano M, Barry C, Clopath C. Hippocampus. 2026 Sep.
The hippocampus is central to memory and spatial planning.
- Sep 2026PMID: 42679734
From gut leakage to memory loss: environmental 2,4-DTBP triggers neuroinflammation through the gut-brain axis in zebrafish.
Gao H, Zhang M, Liang X, et al.. Environ Int. 2026 Sep.
Despite widespread environmental detection of 2,4-di-tert-butylphenol (2,4-DTBP), its neurotoxic impacts on cognitive behavior remain largely unexplored. In this study, adult zebrafish were exposed to 0.01, 0.1, and 1 μM 2,4-DTBP for 28 days.
- Sep 2026PMID: 42425184
UPLC-ESI-qTOF-MS metabolomic characterization and in vivo neuroprotective activity of Diplotaxis harra ethanolic extract through antioxidant, anti-cholinesterase, and anti-amyloid mechanisms.
Taher RF, Abd Elkarim AS, El-Fadaly AA, et al.. Fitoterapia. 2026 Sep.
Aluminum chloride (AlCl3)-induced neurotoxicity is a widely used model of Alzheimer's disease, featuring oxidative stress, cholinergic dysfunction, amyloid deposition, and cognitive deficits.
- Aug 2026PMID: 42546762
Integrated decoding of local and prospective spatial representations for future decision prediction.
Wang X, Luo X, Wang Y, et al.. J Neural Eng. 2026 Aug 26.
Objective.Decoding future spatial decisions from the brain's cognitive map represents a critical step toward cognitive brain-computer interfaces (BCIs) and closed-loop neuromodulation for neurological disorders.
- Aug 2026PMID: 42641960
Dissociable roles of lateral orbitofrontal and medial prefrontal cortex in risk-based decision-making under equal expected value in rats.
Yang YH, Chen CY, Chen SF, et al.. Behav Brain Res. 2026 Aug 25.
The prefrontal cortex (PFC) plays a critical role in decision-making under uncertainty.
§ 4
Discussion
Limitations of the paradigm, methodological caveats, and current directions.
4.1 Common confounds
Variables that can shift T Maze results apart from the effect under study.
Side preference
A fixed left or right preference can dominate choice accuracy, especially in early training.
Correction trials
Including correction trials in accuracy can inflate performance or obscure perseveration unless reported separately.
Reward motivation
Rewarded variants are sensitive to deprivation schedule, reward palatability, and satiety.
Delay sensitivity
Longer delay periods increase memory load and should not be pooled with zero-delay alternation sessions.
Arm odor
Residual reward or animal scent can bias choices unless the cleaning procedure is consistent.
4.2 Construct validity caveats
T Maze is intentionally simple, but that simplicity makes design decisions visible. A valid page or protocol should state task variant, first-entry criterion, chance level, correction-trial rule, side-bias handling, and delay schedule before summarizing accuracy. 1
4.3 Special considerations
When should I use Y Maze instead?
Use Y Maze when the goal is mostly spontaneous alternation with three-arm exploration and less reliance on doors or reward wells.
When should I use Radial Arm Maze instead?
Use Radial Arm Maze when the experiment needs more spatial locations, baited-arm memory load, and repeat-entry error classification.
Does T Maze require reward?
No. Spontaneous alternation can be run without food reward, but rewarded and delayed variants need stricter motivation and side-bias controls.
4.4 Current directions
Quarterly editorial review of emerging T Maze methodology. Q2 2026
Methods
Cleaner alternation definitions
Protocol pages increasingly distinguish spontaneous, rewarded, and delayed alternation rather than treating all T Maze tasks as equivalent.
Emerging
Door-controlled timing
Automated or semi-automated doors improve reproducibility for forced-choice and delay phases.
Methods
Bias-aware reporting
Side-bias and omission reporting are becoming minimum requirements for interpreting choice accuracy.
Emerging
Compact screening batteries
T Maze is often paired with Y Maze, Open Field, and Rotarod to separate working memory from locomotion and motivation.
§ 5
References
10 selected methods and validation references for T Maze.
- Deacon RMJ, Rawlins JNP. T-maze alternation in the rodent. Nat Protoc. 2006;1(1):7-12. doi:10.1038/nprot.2006.2
- Lalonde R. The neurobiological basis of spontaneous alternation. Neurosci Biobehav Rev. 2002;26(1):91-104. doi:10.1016/S0149-7634(01)00041-0
- Dudchenko PA. An overview of the tasks used to test working memory in rodents. Neurosci Biobehav Rev. 2004;28(7):699-709. doi:10.1016/j.neubiorev.2004.09.002
- Shoji H, et al. Comprehensive behavioral test battery for mice. Curr Protoc Mouse Biol. 2012;2:153-187. Find source
- Hughes RN. The value of spontaneous alternation behavior in laboratory rodents. Behav Pharmacol. 2004;15(4):287-293. Find source
- Dember WN, Fowler H. Spontaneous alternation behavior. Psychol Bull. 1958;55(6):412-428. Find source
- Richman CL, Dember WN, Kim P. Spontaneous alternation behavior in animals: a review. Curr Psychol Res Rev. 1986;5:358-391. Find source
- Douglas RJ. The hippocampus and behavior. Psychol Bull. 1967;67(6):416-442. Find source
- Olton DS. Mazes, maps, and memory. Am Psychol. 1979;34(7):583-596. Find source
- Kraeuter AK, Guest PC, Sarnyai Z. The Y-Maze for assessment of spatial working and reference memory in mice. Methods Mol Biol. 2019;1916:105-111. Find source
T Maze
$1,790.00
Added to quoteView Quote
