Conclusions No functional FANCA protein was found in these 3 cases of FA-A, and intragenic deletion, frame shift and splice site mutation were the major pathogenic mutations found in FANCA gene.
结论3例FA-A型患者均无功能性FANCA蛋白表达；基因缺失、移码突变和剪切位点突变是FANCA基因的主要失活方式。
The measurements utilize a dual-channel system to detect the relevant frequency shift. The AFP antibody is immobilized to the crystal surface via protein a.
实验采用双通道系统进行频率变化的测定，并采用蛋白a在晶体固定afp抗体。
Moreover, the electrophoretic mobility shift assay analysis demonstrated that the HuH-7 nuclear proteins form a specific protein-DNA complex composed of LS2 motif.
进一步以胶体电泳位移分析法证实，在LS2 区域会形成HuH-7 核蛋白及DNA的复合物。
Moreover, the electrophoretic mobility shift assay analysis demonstrated that the HuH-7 nuclear proteins form a specific protein-DNA complex composed of LS2 motif.
进一步以胶体电泳位移分析法证实，在LS2 区域会形成HuH-7 核蛋白及DNA的复合物。
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