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。

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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。

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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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