发明名称 |
Method for in vitro assay of soluble fibrin by generating specific degradation products |
摘要 |
The invention concerns a method for assaying soluble fibrin in a sample, in which said sample is brought into the presence of a plasminogen activator with a high specificity for soluble fibrin (PA-Fb sp) and the soluble fibrin count in the sample is measured by measuring the difference between the count of fibrin degradation products obtained after degrading soluble fibrin with PA-Fb sp and the base count of fibrin degradation products determined before bringing the sample into the presence of PA-Fb sp. |
申请公布号 |
US8883433(B2) |
申请公布日期 |
2014.11.11 |
申请号 |
US200310373614 |
申请日期 |
2003.02.25 |
申请人 |
Societe Diagnostica-Stago;Assistance Publique-Hopitaux de Paris |
发明人 |
Mirshahi Bibi Shah Soltan;Soria Jeannette |
分类号 |
G01N33/86;G01N33/53 |
主分类号 |
G01N33/86 |
代理机构 |
Lerner, David, Littenberg, Krumholz & Mentlik, LLP |
代理人 |
Lerner, David, Littenberg, Krumholz & Mentlik, LLP |
主权项 |
1. A method for assaying soluble fibrin in a sample, comprising:
measuring a difference in a count of D-dimer fibrin degradation products between a sample including Plasminogen Activator with a high specificity and/or high affinity for soluble Fibrin (PA-Fb sp) and said sample excluding said PA-Fb sp, wherein said sample which includes PA-Fb sp is incubated for minutes at 37° C. in the presence of a PA-Fb sp and said difference is then measured, wherein said PA-Fb sp is tissue plasminogen activator (t-PA) in a final concentration of about 1 μg/ml to about 2.5 μg/ml of the sample or is staphylokinase (SAK) in a final concentration of about 1 μg/ml to about 12 μg/ml of the sample. |
地址 |
FR |