ELISA PLATE

  • 网络酶标板
ELISA PLATEELISA PLATE
  1. 1 mL of cell suspension was obtained from each group to place into 96-pore ELISA plate , so as to detect the absorbance of each pore at the wavelength of 490 nm in ELISA meter and determine the vigor of NSCs .

    从每组取1mL细胞悬液移入96孔酶标板,在酶联免疫检测仪490nm波长处测定各孔吸光度值,检测神经干细胞活力。

  2. And with the CL-BSA immunized mice to produce antibodies , using CL-OVA-coated elisa plate , Detection of antibodies can be obtained free of CL specific binding reaction occurs . ( 2 ) CL-BSA was prepared as antigen to immunize BALB / C mice .

    而且用CL-BSA免疫小鼠制备抗血清,用CL-OVA包被酶标板,检测得到的抗体可以和游离的CL发生特异性的结合反应。

  3. Comparison Of Reusing Of ELISA Plate Processed With Different Cleaning Solutions

    不同清洗液再生ELISA反应板效果的比较

  4. ELISA plate was coated with soluble scFv and was blocked with BSA .

    以可溶性抗NP单链抗体包被酶标板,BSA封闭酶标板。

  5. And diluted in 1:16 , as SAT ( serum agglutination text ) antigen , thus establishing ELISA , plate agglutination text , and SAT for detection of bovine brucellosis .

    把细胞壁抗原作1∶16稀释用作试管凝集试验抗原,分别建立了牛布氏杆菌ELISA试验、平板凝集试验和试管凝集试验。

  6. The sensitivity of HRP enzyme conjugated antibody in ELISA matrix tests on optical self-encoding microbeads proves 62.5 times higher than on 96-wells ELISA plate .

    而在辣根氧化物酶标显色时,相同条件下光谱自编码微球的检测灵敏度62.5倍于96孔酶标比色板。

  7. A sandwich ELISA for detection of AIV antigen was developed by using purified chicken anti-AIV IgG coated on the ELISA plate and rabbit anti-AIV IgG as the second antibody .

    以纯化的鸡抗AIVIgG为包被抗体,兔抗AIVIgG为第二抗体,建立了检测AIV抗原的夹心ELISA法。