Literature DB >> 579495

The rapid fibrin plate - a method for plasminogen activator assay.

N A Marsh, P J Gaffney.   

Abstract

Most of the technical problems associated with the fibrin plate method have been overcome in recent years with the exception of the long incubation period. This study was carried out to investigate plasminogen-enrichment as a means of shortening this period. Fibrin plates made up to contain 2.0 casein units of added plasminogen each, were opaque, firm, did not lyse spontaneously and yielded biometrically-valid parallel-line assays for streptokinase and urokinase after a 3 hour incubation period. Urokinase assays were more accurate than those for streptokinase probably because of the latter's shallow dose-response curve. Plasminogen-enrichment appears therefore to be a convenient way of producing a "rapid" fibrin plate requiring incubation for 3 hours compared with the usual 16 to 20 hours.

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Year:  1977        PMID: 579495

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  2 in total

1.  Plasminogen activator in cultured Lewis lung carcinoma cells measured by chromogenic substrate assay.

Authors:  P Whur; M Magudia; J Boston; J Lockwood; D C Williams
Journal:  Br J Cancer       Date:  1980-08       Impact factor: 7.640

2.  Biological activity analysis of native and recombinant streptokinase using clot lysis and chromogenic substrate assay.

Authors:  Arash Mahboubi; Seyyed Kazem Sadjady; Mohammad Mirzaei Saleh Abadi; Saeed Azadi; Roya Solaimanian
Journal:  Iran J Pharm Res       Date:  2012       Impact factor: 1.696

  2 in total

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