The extracellular organic matrix of developing human enamel is compose
d of two major classes of proteins, the hydrophobic amelogenins and th
e acidic enamelins. In order to identify, purify, and characterize the
amelogenins from this complex mixture of proteins, and to study their
ultrastructural localization and their pathways of synthesis, secreti
on, and degradation, specific and sensitive probes are needed. In the
present paper the production of a monoclonal antibody against human am
elogenin employing an intrasplenic primary immunization protocol is de
scribed. The monoclonal antibody produced is IgM and recognizes major
human amelogenin protein bands in Western immunoblot assays. It also r
ecognizes amelogenin protein bands from other species, specifically bo
vine and porcine. Indirect immunohistochemical studies showed the mono
clonal antibody to react specifically with the extracellular matrix of
human developing enamel. It did not react with the underlying dentin
layer.