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酶免疫测定法在凝血检测中的应用。

Application of enzyme immunoassays to coagulation testing.

作者信息

Amiral J, Adalbert B, Adam M

出版信息

Clin Chem. 1984 Sep;30(9):1512-6.

PMID:6380814
Abstract

Enzyme immunoassays are very useful for the detection of low concentrations of coagulation proteins and pathological markers in plasma. Analytes in the ng/mL range are measurable with good reproducibility with intra- and interassay CVs of less than 5% to 10%. "Sandwich" methods have been developed for von Willebrand factor (plasma concentration about 8 micrograms/mL, Factor IX (5 micrograms/mL), protein C (4 micrograms/mL), and Factor X (10 micrograms/mL). However, this technique is only suitable for macromolecules; for low-molecular-mass peptides such as fibrinopeptide A a competitive method is used. Normal concentrations of fibrinopeptide A are below 3 ng/mL, with greater values suggesting in vivo generation of thrombin; thus this test is quite useful in detecting thrombosis. Reagents for both the sandwich and competitive methods are commercially available and cost effective, and have a longer shelf-life than those for radioimmunoassays.

摘要

酶免疫测定法对于检测血浆中低浓度的凝血蛋白和病理标志物非常有用。纳克/毫升范围内的分析物可进行测量,批内和批间变异系数小于5%至10%,具有良好的重现性。已开发出“夹心”方法用于检测血管性血友病因子(血浆浓度约8微克/毫升)、因子IX(5微克/毫升)、蛋白C(4微克/毫升)和因子X(10微克/毫升)。然而,该技术仅适用于大分子;对于低分子量肽,如纤维蛋白肽A,则使用竞争法。纤维蛋白肽A的正常浓度低于3纳克/毫升,浓度升高表明体内有凝血酶生成;因此,该检测在检测血栓形成方面非常有用。夹心和竞争法的试剂均可从市场上购得,且性价比高,保质期比放射免疫测定法的试剂更长。

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