| Literature DB >> 27911379 |
Haochuan Zhang1, JunGang Huang2, Xin Liu3, Ping Zhu4, Zhongrong Li5, Xue Li6.
Abstract
High-resolution episcopic microscopic (HREM) technology enables rapid acquisition of high-resolution digital volumetric and three-dimensional (3D) morphometric data. Here, we describe the detailed protocol to image the entire mouse embryo. The protocol consists of four major sections: sample preparation, embedding, image acquisition and finally, 3D visualization. The technology requires specimens to be stained with a fluorescent dye, which can be problematic for large or dense specimens. To overcome this limitation, we have improved the existing protocol to enhance tissue penetration of the dye by pretreating the specimen with a solution containing urea and sodium dodecyl sulfate. The protocol uses only routine laboratory equipment and reagents for easy adaptation in standard laboratory settings. We show that the resulting high-resolution 3D images faithfully recapitulate the detailed morphologic features of the internal organs of mouse embryos, thereby permitting morphometric analyses. Together, we present a detailed and improved protocol using standard laboratory equipment to acquire high-resolution 3D images of small and large sized specimens.Entities:
Mesh:
Year: 2016 PMID: 27911379 PMCID: PMC5226265 DOI: 10.3791/54625
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355