预期应用
ELISA法定量测定人血清、血浆、细胞培养物上清或其它相关液体中8-iso-PG-F2a含量。
实验原理
本试剂盒应用双抗体夹心酶标免疫分析法测定标本中8-iso-PG-F2a水平。用纯化的抗体包被微孔板，制成固相抗体，往包被单抗的微孔中依次加入8-iso-PG-F2a抗原、生物素化的抗人8-iso-PG-F2a抗体、HRP标记的亲和素，经过彻底洗涤后用底物TMB显色。TMB在过氧化物酶的催化下转化成蓝色，并在酸的作用下转化成最终的黄色。颜色的深浅和样品中的8-iso-PG-F2a呈正相关。用酶标仪在450nm波长下测定吸光度（OD值），计算样品浓度。
Intended use
This immunoassay kit allows for the specific measurement of human 8-iso-PG-F2a concentrations in cell culture supernates, serum, and plasma.
Test principle
This assay employs the quantitative sandwich enzyme immunoassay technique. A monoclonal
antibody specific for 8-iso-PG-F2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any 8-iso-PG-F2a present is bound by the immobilized antibody. An
enzyme-linked monoclonal antibody specific for 8-iso-PG-F2a is added to the wells. Following a wash to remove any unbound antibody-enzyme reagent, a substrate solution is added to the wells
and color develops in proportion to the amount of 8-iso-PG-F2a bound in the initial step. The color
development is stopped and the intensity of the color is measured.
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