The antigen-antibody complex here was precipitated with saturated ammonium sulfate solution in a final saturation 37.5%.
沉淀抗原—抗体复合物的饱和硫酸铵最终饱和度为37.5%。
Objective To prepare monoclonal antibody (McAb) against neoantigen of the human complement membrane attack complex (MAC).
目的研制针对人补体膜攻击复合物(MAC)新抗原的特异性单克隆抗体。
Because the analyte molecules are recognized by forming the binding complex with antibody, a decrease in the detection limit is achieved only by an increase in the reaction yield.
因为分析物分子能通过与抗体形成结合物而被发现,所以降低检测极限只能通过增加反应产率来达到。
The antibody then participates in the binding reaction to form a complex with the analyte in the liquid phase.
然后抗体参与结合反应,在水溶液中形成了带有分析物的复合物。
This complex moves forward continuously until it is eventually captured by the antibody immobilized on the surfaces of the nitrocellulose membrane.
这个复合物继续前移,直到被固定在硝酸纤维素表面的抗体捕获为止。
The capture of the labeled antibody-analyte complex for signal generation can be achieved with the antibody immobilized in a defined area of nitrocellulose membrane as mentioned.
对产生信号的标记抗体-抗原复合物的捕获,是用抗体固定在已经提到的硝酸纤维素的特定区域内来达到的。
Methods The antibody-targeted complex could be prepared by mixing SPA-PLL conjugate, oligodeoxy nucleotide and anti-CD44 antibody based on their optimal mass ratio.
方法将SPA-PLL交联物、CD44抗体和反义寡核苷酸以适宜的质量比混合即可组装成抗体靶向寡核苷酸复合物;
This permits the formation of binding complex between the labeled antibody and analyte in the void space of glass fibers.
这就使得标记抗体和分析物间结合物的形成在玻璃纤维的空的空间里进行的。
Methods:A double mono-clonal antibody sandwich enzyme-linked immunosorbent assay(ELISA)was used to detect the circulating antigens, antibodies and immune complex in 109 sera of neurocysticercosis.
方法:用ELISA法检测109例脑囊尾蚴病患者血清抗原、抗体及循环免疫复合物。
The detection antibody-analyte complex formation is enhanced by inserting a reaction pad between the glass strip and the capture membrane.
在玻璃条和捕获膜之间加入一个反应垫,可以增强检测物抗体抗原结合物的形成。
The detection antibody-analyte complex formation is enhanced by inserting a reaction pad between the glass strip and the capture membrane.
在玻璃条和捕获膜之间加入一个反应垫,可以增强检测物抗体抗原结合物的形成。
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