发明名称
摘要 NEW MATERIAL:The peptide of formula I (W is Met; X is Ala; Y is 11 amino acid polypeptide residue of human fibronectin having the sequence of formula II; Z is 132 amino acid polypeptide residue of fibrin-bonded domain at the C- terminal side of human fibronectin having the sequence of formula III; (l), (m) and (n) are 0 or 1). USE:A blood coagulation inhibitor. A material for drug-delivery system. PREPARATION:The objective polypeptide of formula I can be produced e.g. by treating a cDNA fragment coding the 143 amino acid sequence at the C- terminal side of human fibronectin (FN) with a restriction enzyme, subjecting the treated product to agarose gel electrophoresis, recovering the fragments of 0.96kb and 405kb, bonding the fragments to an adaptor, conjugating to a vector, cloning the product, transducing into E.coli to effect transformation and culturing the resultant transformant.
申请公布号 JP2829397(B2) 申请公布日期 1998.11.25
申请号 JP19890262131 申请日期 1989.10.09
申请人 TAKARA SHUZO KK 发明人 NODA AKIHIRO;OKAZAWA KAZUHIDE;ICHIMURA NOBUKO;KIMIZUKA FUSAO;KATO IKUNOSHIN
分类号 C12N15/09;A61K38/00;A61K38/16;A61P7/02;A61P43/00;C07H21/04;C07K14/745;C12N1/21;C12N15/12;C12P21/02;C12R1/19;(IPC1-7):C12N15/09 主分类号 C12N15/09
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