| Literature DB >> 6809413 |
Abstract
Antisera were raised against the long and short form of mouse and human 7-S collagen and against type IV collagens solubilized by acid extraction or limited digestion with pepsin. All the antisera showed strong binding for 7-S collagen in radioimmunoassays demonstrating that the 7-S domain which serves as a cross-linking region of type IV collagen is the most immunogenic portion of the molecule. Cross-reaction studies and analysis of fragments showed a complex antigenic structure including some determinants common to the long and short form of 7-S collagen and others unique for the long form. Purified antibodies against 7-S collagen reacted in indirect immunofluorescence with almost all basement membranes of the body indicating that the 7-S domain is a common structural element of type IV collagens.Entities:
Mesh:
Substances:
Year: 1981 PMID: 6809413 DOI: 10.1016/s0174-173x(81)80026-x
Source DB: PubMed Journal: Coll Relat Res ISSN: 0174-173X