Specific identification of fibrin(ogen) degradation products in plasma and serum using blotting and peroxidase labeled antiserum

Anna B. Proietti, Maura Mcguire, William Bell

Research output: Contribution to journalArticle

Abstract

We describe a method for identifying fibrinogen and fibrin split products using electrophoresis on agarose gel with sodium dodecyl sulfate (SDS) followed by blotting in nitrocellulose paper. Detection of these derivatives after blotting is accomplished with per‐oxidase‐conjugated rather than by isotopically labeled antibodies. This technique can detect diverse fibrinogen derivatives produced in vivo or in vitro by the combined action of thrombin, plasmin, and factor XIII. This methodology is applicable to plasma, serum, and other body fluids including urine and ascitic fluid. This sensitive and specific assay, distinguishing the products of cross‐linked fibrin from those of fibrinogen and detecting fibrin polymers in plasma, can be achieved without the use of radioactivity.

Original languageEnglish (US)
Pages (from-to)270-274
Number of pages5
JournalAmerican Journal of Hematology
Volume34
Issue number4
DOIs
StatePublished - Jan 1 1990

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Fibrin Fibrinogen Degradation Products
Fibrin
Fibrinogen
Peroxidase
Immune Sera
Factor XIII
Collodion
Agar Gel Electrophoresis
Ascitic Fluid
Fibrinolysin
Body Fluids
Serum
Thrombin
Sodium Dodecyl Sulfate
Radioactivity
Polymers
Urine
Antibodies
estropipate
In Vitro Techniques

Keywords

  • electrophoresis
  • fibrinogen
  • immunoblotting
  • peroxidase

ASJC Scopus subject areas

  • Hematology

Cite this

Specific identification of fibrin(ogen) degradation products in plasma and serum using blotting and peroxidase labeled antiserum. / Proietti, Anna B.; Mcguire, Maura; Bell, William.

In: American Journal of Hematology, Vol. 34, No. 4, 01.01.1990, p. 270-274.

Research output: Contribution to journalArticle

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