Ahnfelt-Rønne Jonas, Jørgensen Mette C, Hald Jacob, Madsen Ole D, Serup Palle, Hecksher-Sørensen Jacob
Department of Developmental Biology, Hagedorn Research Institute, Gentofte, Denmark.
J Histochem Cytochem. 2007 Sep;55(9):925-30. doi: 10.1369/jhc.7A7226.2007. Epub 2007 May 3.
We have developed a wholemount immunofluorescence protocol for the simultaneous detection of up to three proteins in mouse and chicken embryos. Combined with Murray's clearing reagent (BABB) and microscope objectives with long working ranges and high numerical apertures mounted on a confocal microscope, cellular resolution can be obtained in depths offering the possibility of examining expression patterns in entire organs or embryos. Three-dimensional projections of the optical confocal sections can be computed with computer software allowing rotation around any axis. The protocol is robust and we find that most antibodies working on tissue sections also work with this protocol. This manuscript contains online supplemental material at http://www.jhc.org. Please visit this article online to view these materials.
我们开发了一种全组织免疫荧光方法,用于同时检测小鼠和鸡胚胎中的多达三种蛋白质。结合默里透明剂(BABB)以及安装在共聚焦显微镜上具有长工作距离和高数值孔径的显微镜物镜,可以在一定深度获得细胞分辨率,从而有可能检查整个器官或胚胎中的表达模式。光学共聚焦切片的三维投影可以通过计算机软件计算得出,允许围绕任何轴进行旋转。该方法很可靠,并且我们发现大多数在组织切片上有效的抗体在此方法中也适用。本文稿在http://www.jhc.org上包含在线补充材料。请在线访问本文以查看这些材料。