High-Resolution Episcopic Microscopy / Applications / Heart Imaging
3D Heart Imaging in Mouse
Embryos & Animal Models
Gap-free 3D datasets of cardiac structures at 1–6 micron voxel resolution, from early cardiac looping at E9.5 through to adult ventricular morphology. HREM delivers the structural clarity required for cardiovascular research, congenital heart defect characterisation and cardiac phenotyping in gene knockout models.

Mouse Heart 3D Credit: Dr. Aseel Abbad (University of Nottingham, UK)
Multi
SAMPLES PER RUN
High-throughput imaging
Multiple embryos per block, practical for knockout cohort studies
360°
CARDIAC ANATOMY
Complete 3D architecture
Chambers, valves, septa, outflow tracts, all in correct spatial context
1µm
OPTICAL RESOLUTION
Resolution
Resolves valve leaflets and trabecular architecture beyond conventional techniques
2D+3D
FROM ONE ACQUISITION
Single dataset
Section review and 3D reconstruction from the same HREM run
3D CARDIAC IMAGING IN MOUSE EMBRYOS, PUPS, ADULT MICE & CHICKEN EMBRYOS
3D heart imaging in small animal models with HREM
High-Resolution Episcopic Microscopy (HREM) is a block-face 3D imaging technique that produces complete, registered datasets of cardiac structures in small animal models, without section loss, compression artefacts, or the registration errors that affect conventional histology reconstructions.
HREM is particularly well suited to cardiac imaging because the heart's complex 3D architecture interlocking chambers, thin-walled septa, valve leaflets and vessel origins cannot be reliably characterised from 2D sections alone. A complete volumetric dataset allows researchers to assess structural relationships, measure cavity volumes, and identify subtle morphological variants that would be missed or misclassified in conventional serial histology.
Whether you are studying embryonic mouse heart development across the E9.5–E18.5 morphogenesis window, characterising congenital heart defects (CHD) in knockout lines, or performing comparative cardiac anatomy in chicken embryo models, HREM provides the resolution and 3D context required.
HOW HIGH-RESOLUTION EPISCOPIC MICROSCOPY ENHANCES 3D HEART IMAGING
What HREM delivers that other methods cannot
Cardiac structures require complete 3D context to be reliably characterised. HREM provides four capabilities that make it the preferred technique for cardiovascular research in small animal models worldwide.
Multi
samples per run
High-throughput cardiac imaging
HREM supports multiple samples per imaging run using scanning stages, making it practical for knockout phenotyping trials and large cohort studies. Datasets are acquired consistently and are directly comparable across animals, reducing the operator variability that affects manual histology workflows.
360°
cardiac anatomy
Complete 3D cardiac anatomy
HREM resolves the full cardiac architecture including ventricular and atrial chambers, atrioventricular and semilunar valves, interventricular and interatrial septa, outflow tracts and great vessel origins. Structures are captured in their correct spatial relationships, supporting accurate classification of complex congenital malformations.
3D
quantitative
measurement
Quantitative volumetric analysis
Unlike optical methods that degrade with depth, HREM resolution is consistent across the entire z-depth of the sample, because each image is acquired from the freshly cut block face rather than through intervening tissue. This enables reliable ventricular volume measurement and morphometric analysis.
JB-4
resin embedded
Consistent, reproducible contrast
HREM produces contrast that is consistent across samples and acquisition runs. Without the variability of immunostaining, datasets from different animals and timepoints can be compared directly, a critical advantage for regulated preclinical workflows and multi-site studies.

HREM heart sample datasets
Mouse heart 3D reconstructions at different developmental stages from E9.5 through to postnatal pup and adult. All imaged with HREM at 1–6 micron resolution.
IMAGING HEART DEVELOPMENT IN MOUSE AND EMBRYO MODELS
3D cardiac datasets across the full developmental window
High-Resolution Episcopic Microscopy provides precise 3D datasets of cardiac structures in mouse and chicken embryos, with sample sizes ranging from under 1mm up to 25mm. The technique covers the complete E9.5–E18.5 morphogenesis window, from early cardiac looping and chamber formation through to mature ventricular morphology in late-stage embryos.
HREM supports both 2D section review (for histological assessment) and complete 3D reconstruction from the same dataset, without a second acquisition run. This makes it practical for developmental biology, phenotyping and cardiovascular structural research within a single imaging workflow.
Benefits of HREM for cardiac imaging
HREM has become the standard 3D imaging technique for cardiovascular phenotyping in mouse models across research groups worldwide. Here is why.
Optical resolution to 1µm
Resolves vessel walls, valve leaflet margins and trabecular architecture at a level of detail difficult with micro-CT on unstained tissue. This resolution is critical for characterising thin-walled structures such as the interatrial septum, membranous ventricular septum and valve leaflets in embryonic hearts.
Repeatable and standardised
The block-face acquisition method is inherently reproducible. Without clearing or staining variability, results are consistent across operators, runs and timepoints making HREM suitable for regulated preclinical workflows, multi-site studies and longitudinal developmental comparisons.
Dense tissue compatibility
Myocardial tissue, vessel walls and partially mineralised structures in older specimens are all imaged with consistent contrast with no clearing required, no tissue-dependent degradation of image quality. Unlike light sheet microscopy, HREM works equally well for dense and mineralised cardiac tissue.
2D and 3D from a single acquisition
Every HREM run produces both a complete stack of 2D section images and the raw data for 3D reconstruction. Researchers can review individual sections for histological assessment and generate 3D models from the same dataset, no second acquisition needed, no additional sample processing.

APPLICATIONS OF HREM IN CARDIOVASCULAR RESEARCH
HREM cardiac imaging applications
HREM allows researchers to study heart development and disease in animal models across a broad range of research programmes.
Heart development in mice
HREM enables detailed 3D imaging of heart development in mice, from early cardiac looping at E9.5 through to complete four-chamber morphology at E18.5. Developmental staging, chamber growth and septal formation can all be characterised volumetrically from a single acquisition.
Chicken embryo heart imaging
HREM is effective for imaging chicken embryo cardiovascular systems, providing valuable data for comparative cardiac studies. Chicken embryo hearts at HH stages provide accessible, large model systems for studying cardiac looping, valve formation and outflow tract development.
Congenital heart defect characterisation
HREM is widely used to characterise congenital heart defects (CHD) in gene knockout mouse lines. VSD, AVSD, transposition of the great arteries, double outlet right ventricle and other complex malformations can be classified reliably from 3D HREM datasets where 2D histology would be ambiguous.
Large cohort phenotyping screens
HREM is routinely used in large-scale cardiac phenotyping programmes where embryonic lethal or sub-lethal lines require rapid, standardised 3D cardiac characterisation. Multi-sample scanning stages allow several embryos per block, making screen-scale cardiac phenotyping practical.
Mouse embryo cardiac imaging
Image the full embryo at cardiac imaging resolution, making it possible to study the heart at various stages of embryonic development (E9.5–E14.5) in the context of the surrounding anatomy. Whole-embryo HREM datasets support both cardiac and extracardiac phenotyping from the same run.
Larger cardiac samples pups & adult mice
HREM can be used to image denser larger cardiac systems such as postnatal pups and adult mice, supporting small animal heart imaging and 3D tissue morphology analysis. Sample sizes up to 25mm are accommodated as standard; larger samples on request.
Frequently asked questions
Questions we receive from cardiovascular researchers, core facility managers and phenotyping programme leaders about HREM for cardiac imaging.
What makes HREM a good tool for heart imaging in small models?
HREM provides high resolution, consistent contrast and complete 3D imaging of the cardiac architecture in small animal models, at a level of detail and reproducibility not achievable with conventional histology or micro-CT. The heart's complex 3D structure (interlocking chambers, thin septa, valve leaflets) requires volumetric data to be reliably characterised. HREM produces a registered, gap-free dataset from which both 2D sections and 3D reconstructions can be derived. Resolution to 1µm resolves structures such as the membranous ventricular septum and valve leaflet margins that micro-CT cannot distinguish in unstained tissue.
Can HREM be used for imaging hearts at different developmental stages?
Yes, HREM covers the complete E9.5–E18.5 mouse embryo developmental window as standard, from early cardiac looping and chamber formation through to mature four-chamber morphology in late-stage embryos. It also accommodates postnatal pups and adult mice for cardiac imaging. Chicken embryo cardiovascular systems at multiple HH stages are also compatible. Contact us with your specific developmental stage and sample size for confirmation.
How does HREM compare to micro-CT for mouse heart imaging?
HREM offers significantly superior soft tissue contrast for cardiac imaging compared to micro-CT, without contrast agents. Micro-CT excels for bone and mineralised structures but struggles to resolve thin soft tissue structures (valve leaflets, membranous septum, trabecular architecture) in unstained cardiac specimens. HREM provides 1µm resolution with histology-quality contrast at a cost point that is more accessible than high-resolution micro-CT for cardiac applications. Many cardiovascular research groups use both techniques: micro-CT for bone/vessel structure, HREM for soft tissue cardiac detail.
Can HREM show congenital heart defects reliably?
Yes — HREM is widely used as the gold-standard imaging method for congenital heart defect (CHD) characterisation in mouse knockout lines. Defects including ventricular septal defects (VSD), atrioventricular septal defects (AVSD), transposition of the great arteries (TGA), double outlet right ventricle (DORV) and persistent truncus arteriosus can all be reliably classified from 3D HREM datasets. The 3D spatial context is essential, many of these defects cannot be unambiguously classified from 2D histological sections, where the apparent anatomy depends entirely on the plane of section.
Is HREM suitable for large-scale cardiac phenotyping screens
Yes, HREM is routinely used in large-scale cardiac phenotyping programmes. Multi-sample scanning stages allow several embryos to be embedded and imaged in a single block, significantly increasing throughput. The inherently reproducible block-face method means datasets are directly comparable across animals within a cohort without operator-dependent staining variability. A single HREM acquisition run can replace weeks of serial histology sectioning for cardiac phenotyping purposes.
Can HREM be used to image other species and organs?
Yes, HREM is not limited to mouse heart imaging. Chicken embryos, zebrafish, rat embryos and other small vertebrate species are all compatible within the standard sample size range (under 1mm to 25mm). Other organs including brain, kidney, liver, lung and gut are regularly imaged using HREM. OHREM systems extend specimen size beyond 25mm for larger biological material. See our mice and zebrafish application page and all HREM applications for further detail.
Do you supply HREM systems for cardiac research worldwide?
Yes, Indigo Scientific supplies HREM and OHREM systems worldwide to cardiovascular research groups, developmental biology departments, core imaging facilities and pharmaceutical preclinical teams. We work with groups across Europe, North America, Asia and beyond. Contact us to discuss your cardiac imaging requirements, specimen types and throughput needs, we will advise on the right system and support arrangement for your location.
Contact our High-Resolution Episcopic Microscopy (HREM) Experts
Want to know more about HREM, ask for a quote or get questions answered. Contact us and we can help answer all your questions.
Phone:
+44(0) 1462633500
Email:
hello@indigo-scientific.co.uk







