Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated 54 min ago
Peer-reviewedCC BYBio-protocol

Protocol for Mouse Embryonic Aorta-Gonad-Mesonephros (AGM) Region Frozen Sectioning and Immunofluorescence.

  1. 1School of Life Science and Technology, Shandong Second Medical University, Weifang, China.

Abstract

The aorta-gonad-mesonephros (AGM) region is the site where hematopoietic stem cells (HSCs) first emerge during development, and is therefore widely used to study in vivo hematopoiesis and to discover novel regulatory mechanisms. The endothelial-to-hematopoietic transition (EHT) process can be directly observed via immunofluorescence on frozen sections of the AGM region. However, the mouse AGM region is extremely delicate and lies deep within the embryo, between the notochord and the somatic mesoderm. Here, we present a step-by-step protocol covering embryo collection, fixation, dehydration, and embedding with a defined orientation, followed by frozen sectioning, immunofluorescence staining, and confocal imaging. The protocol is highly reproducible and easy to follow and provides clear instructions on orienting the embryo and anatomically locating AGM. By filling a technical gap, the protocol can enable researchers to reliably study HSC emergence and EHT in the mouse embryonic AGM. Key features • Provides detailed instructions on embryo embedding orientation and microscopic observation during cryosectioning to precisely locate the mouse AGM region. • Covers all steps from embryo harvesting, cryosectioning, and immunofluorescence to confocal imaging, ensuring high reproducibility. • Developed for delicate mouse embryonic AGM tissue (e.g., E9.5-E11.5), enabling direct observation of EHT via immunofluorescence.

Related

  1. Protocol for 3D-guided sectioning and deep cell phenotyping via light sheet imaging and 2D spatial multiplexing
    Kevin Bigott, Victoria H Schoppel, Manuel Martinez-Osuna +8
    STAR ProtocolsPeer-reviewedCC BY-NC-ND 4.0Full text3 citedBiophysicsHAL
  2. Protocol for precise large-region haplotype modification for isogenic human iPSC generation using CRISPR-Cas9
    Manoj K. Mishra, Rajan Pandey, Bhavika Therani +3
    STAR ProtocolsPeer-reviewedCC BY-NC 4.0Full textMolecular biology & gene regulationPMC
  3. Immunofluorescence: quantitative considerations.
    Joost J. Haaijman
    PubMedPeer-reviewedLicence not stated10 citedBiophysicsOpenAlex
  4. Symmetric Off-Axis Spectral Encoding Enables High-Throughput Six-Color Optical Sectioning Imaging.
    Jiangjiang Zhao, Zhangheng Ding, Zhan Zhang +3
    Nanophotonics (Berlin, Germany)Peer-reviewedCC BYFull textBiophysicsEurope PMC
  5. Microtube-Assisted Paraffin Embedding and Sectioning of Fragile 3D Tumor Spheroids for High-Quality Histology
    Ramón Cervantes-Rivera, Sandra Jetsamari Figueroa Ortiz, Atalia Ziret Romero Rosas +6
    Bio-protocolPeer-reviewedCC BY-NC 4.0Full textMolecular biology & gene regulationPMC
BibTeX
@article{jia2026protocol,
  title = {{Protocol for Mouse Embryonic Aorta-Gonad-Mesonephros (AGM) Region Frozen Sectioning and Immunofluorescence.}},
  author = {Yan Jia and Sixuan Huo and Mei Li},
  journal = {Bio-protocol},
  year = {2026},
  month = sep,
  doi = {10.21769/bioprotoc.5828},
  url = {https://europepmc.org/article/MED/42996781},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Protocol for Mouse Embryonic Aorta-Gonad-Mesonephros (AGM) Region Frozen Sectioning and Immunofluorescence.
AU  - Yan Jia
AU  - Sixuan Huo
AU  - Mei Li
PY  - 2026
DA  - 2026/09/20
JO  - Bio-protocol
DO  - 10.21769/bioprotoc.5828
UR  - https://europepmc.org/article/MED/42996781
AB  - The aorta-gonad-mesonephros (AGM) region is the site where hematopoietic stem cells (HSCs) first emerge during development, and is therefore widely used to study in vivo hematopoiesis and to discover novel regulatory mechanisms. The endothelial-to-hematopoietic transition (EHT) process can be directly observed via immunofluorescence on frozen sections of the AGM region. However, the mouse AGM region is extremely delicate and lies deep within the embryo, between the notochord and the somatic mesoderm. Here, we present a step-by-step protocol covering embryo collection, fixation, dehydration, and embedding with a defined orientation, followed by frozen sectioning, immunofluorescence staining, and confocal imaging. The protocol is highly reproducible and easy to follow and provides clear instructions on orienting the embryo and anatomically locating AGM. By filling a technical gap, the protocol can enable researchers to reliably study HSC emergence and EHT in the mouse embryonic AGM. Key features • Provides detailed instructions on embryo embedding orientation and microscopic observation during cryosectioning to precisely locate the mouse AGM region. • Covers all steps from embryo harvesting, cryosectioning, and immunofluorescence to confocal imaging, ensuring high reproducibility. • Developed for delicate mouse embryonic AGM tissue (e.g., E9.5-E11.5), enabling direct observation of EHT via immunofluorescence.
SN  - 2331-8325
ER  -