Monoclonal Antibodies to Bovine Collagenase Inhibitor

Shuji Kodama , Jun-Ichi Kishi , Ken-Ichi Obata , Kazushi Iwata , Taro Hayakawa
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引用次数: 48

Abstract

Hybridoma antibodies against bovine collagenase inhibitor were produced by fusion of myeloma cells NS-1 (P3-NS 1-1) with spleen cells from mice hyperimmunized with collagenase inhibitor purified from the explant medium of bovine dental pulps. Hybridomas positive by an enzyme-linked immunosorbent assay (ELISA) for bovine collagenase inhibitor were cloned by the dilution method. Seventeen hybridomas producing antibodies were isolated, four of which also recognized purified human collagenase inhibitor in the ELISA. Using a monoclonal antibody-Sepharose affinity column, we easily purified both bovine and human collagenase inhibitors to homogeneity. They showed the same mobility on sodium dodecyl sulfate-polyacrylamide gel electrophoresis, corresponding to a molecular mass of 32,000 daltons.

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牛胶原酶抑制剂单克隆抗体
用牛牙髓中纯化的胶原酶抑制剂高免疫小鼠脾细胞,将骨髓瘤细胞NS-1 (P3-NS - 1-1)与脾细胞融合,制备了抗牛胶原酶抑制剂杂杂瘤抗体。用稀释法克隆了牛胶原酶抑制剂酶联免疫吸附试验(ELISA)阳性的杂交瘤。共分离到17个产生抗体的杂交瘤,其中4个在ELISA中也能识别纯化的人胶原酶抑制剂。使用单克隆抗体- sepharose亲和柱,我们很容易地纯化牛和人胶原酶抑制剂,以达到均匀性。它们在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳上显示出相同的迁移率,对应于32,000道尔顿的分子质量。
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