Immunofluorescent staining of Sea Urchin embryos 1. Transfer fixed embryos to microfuge tubes. Allow to settle for 10 minutes. Gently remove most of the liquid. 2. Add 100 ul antibody to one tube and 100 ul 1% normal goat serum to the other as a control. Let sit for 45 minutes at room temperature. Embryos will settle. 3. Remove most of liquid. Add 1 ml SW to wash. Allow to settle, remove liquid.  4. Add 100 ul Fluorescein- or Texas red-congugated anti-mouse IgG (diltuted according to manufacturer's recommendations) to both tubes. Let sit for 45 minutes at room temperature. Embryos will settle. 5. Remove most of liquid. Add 1 ml SW to wash. Allow to settle, remove liquid. Add 100 ul PBS. 6. Transfer 10 ul of each sample to microscope slides. Check that there are embryos. Coverslip. Examine using epifluorescence.   Antibodies from David McClay Ig8, 1D5 -PMCs and spicules Ecto V, 295 - ventral ectoderm 5C7 - vegetal plate and posterior archenteron   Secondary antibody Texas Red-congugated Goat anti-mouse IgG from Jackson ImmunoResearch (1/100) References: Wessel, G.M. and D.R. McClay, (1986) Two embryonic, tisssue-specific moleculaes identified by a double-label immunofluorescence technique for monoclonal antibodies, J. Histochem. Cytochem. 34:703-706. Wessel, G.M. and D.R. McClay,(1985). Sequential expression of germ-layer specific molecules in teh sea urchin embryo. Dev. Biol. 111:451-463. McClay, D. and N. Wessel. 1984. Spacial and temporal appearance and redistribution of cell surface antigens during sea urchin development. in Molecular Biology of Development. Alan R. Liss, Inc., pp.165-184.

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Last Modified: 25 January, 2003

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