Groves Stephanie S, Turell Michael J, Bailey Charles L, Morozov Victor N
The National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA 20110, USA.
Am J Trop Med Hyg. 2008 Jan;78(1):63-9.
To reduce the assay time for detecting virus-specific antibodies in serum, we developed microarray-based active immunoassay techniques for detecting West Nile virus (WNV)-specific IgM molecules in chicken blood. The assay uses electrophoretic concentration of IgM molecules onto WNV antigens arrayed on a dialysis membrane followed by detection of bound IgM molecules with functionalized magnetic beads as active labels. This assay takes only 15 minutes and has the same sensitivity as a commercially available human WNV IgM antibody-capture enzyme-linked immunosorbent assay (commonly called a MAC-ELISA) modified for use with chicken sera.
为缩短检测血清中病毒特异性抗体的检测时间,我们开发了基于微阵列的活性免疫分析技术,用于检测鸡血液中的西尼罗河病毒(WNV)特异性IgM分子。该分析方法利用电泳将IgM分子浓缩到排列在透析膜上的WNV抗原上,然后用功能化磁珠作为活性标记物检测结合的IgM分子。该分析仅需15分钟,并且与经过改进可用于鸡血清的市售人WNV IgM抗体捕获酶联免疫吸附测定法(通常称为MAC-ELISA)具有相同的灵敏度。