Comparisons of red ratings (RR) with Fe_d, Fe_d/Fet, clay content, andmagnetic susceptibility (x) of two loess-paleosol sequences at Luochuan and Lingtai on China's LoessPlateau were conducted to study the possibl...Comparisons of red ratings (RR) with Fe_d, Fe_d/Fet, clay content, andmagnetic susceptibility (x) of two loess-paleosol sequences at Luochuan and Lingtai on China's LoessPlateau were conducted to study the possible relationship between RR and pedogenic degrees of thetwo loess-paleosol sequences, and to discuss whether the RR could become new paleo-climaticindicators. Results showed that the RR of the two loess-paleosol sequences had positive, highlysignificant (P < 0.01) correlations with: 1) citrate-bicarbonate-dithionite (CBD) extracted iron(Fe_d), 2) ratios of CBD extracted iron to total iron (Fe_d/Fet), 3) clay (< 2 mum), and 4) magneticsusceptibility (x). This suggested that the RR of these loess-paleosol sequences could indicatedegreesof loess weathering and pedogenesis and were potential paleo-climatic proxies. The strongcorrelations of RR to Fe_d and x also implied that during pedogenic processes, pedogenic hematite inloess and paleosols were closely related to the amount of total secondary iron oxides and pedogenicferrimagnetic minerals (predominantly maghemite).展开更多
Cardiac troponin I(cTnI) was separated and purified from human left ventricular tissue by affinity chromatographic method and used to immunize Balb/c mice by intraperitoneal injection and four hybridoma cell lines, wh...Cardiac troponin I(cTnI) was separated and purified from human left ventricular tissue by affinity chromatographic method and used to immunize Balb/c mice by intraperitoneal injection and four hybridoma cell lines, which secreted monoclonal antibody(mAb) against human cTnI, were obtained by cell fusion, identification and cloning twice. Three mAbs(9F5, 2F11, 8C12) were produced from the ascites of Balb/c mice injected intraperitoneally the hybridoma cells and characterized by means of a surface plasmon resonance(SPR) biosensor. An optimal and specific sensing membrane for troponin I was prepared with staphylococcal protein A(SPA) as the intermediate layer and mAb against human cTnI as the capture antibody. On the basis of the sensing membrane, two modes of operation of the SPR biosensor were developed, i.e ., a direct detection of antigen antibody affinity and a sandwich assay. In the sandwich assay detection mode, the mAbs competition was measured by monitoring whether the secondary antibody had been attached to the cTnI already captured by the first antibody on the sensor surface. The SPR biosensor was shown to be able to directly detect the antigen antibody affinity and the order of the affinity was found to be 9F5>2F11>8C12. In the sandwich detection mode, it was found that the different epitopes on the cTnI molecules were recognized by the three mAbs respectively, but the asymmetrical competition was shown between 2F11 and 8C12 and no competition was found between 9F5 and 2F11 or 8c12. Based on these results, a double monoclonal sandwich immunoassay for cTnI was developed by using the optimal antibody pair of 9F5 and 2F11 and the SPR biosensor with SPA substrate membrane, which showed an excellent sensitivity of 0.8 μg/L for both the buffer and the serum samples compared with the direct detection of cTnI for the buffer with the lowest detection limit of 4 μg/L and conventional ELISA with the sensitivity of 1.9 μg/L.展开更多
基金Project supported by the National Natural Science Foundation of China (No. 40101013) the Outstanding Overseas Chinese Scholars Fund of the Chinese Academy of Sciences (No. 2003-1-7).
文摘Comparisons of red ratings (RR) with Fe_d, Fe_d/Fet, clay content, andmagnetic susceptibility (x) of two loess-paleosol sequences at Luochuan and Lingtai on China's LoessPlateau were conducted to study the possible relationship between RR and pedogenic degrees of thetwo loess-paleosol sequences, and to discuss whether the RR could become new paleo-climaticindicators. Results showed that the RR of the two loess-paleosol sequences had positive, highlysignificant (P < 0.01) correlations with: 1) citrate-bicarbonate-dithionite (CBD) extracted iron(Fe_d), 2) ratios of CBD extracted iron to total iron (Fe_d/Fet), 3) clay (< 2 mum), and 4) magneticsusceptibility (x). This suggested that the RR of these loess-paleosol sequences could indicatedegreesof loess weathering and pedogenesis and were potential paleo-climatic proxies. The strongcorrelations of RR to Fe_d and x also implied that during pedogenic processes, pedogenic hematite inloess and paleosols were closely related to the amount of total secondary iron oxides and pedogenicferrimagnetic minerals (predominantly maghemite).
基金Supported by National Natural Science Fundation of China(Project No.2 9875 0 10 ) and the Health Department of JilinProvince(Project No.980 4 7) ,China
文摘Cardiac troponin I(cTnI) was separated and purified from human left ventricular tissue by affinity chromatographic method and used to immunize Balb/c mice by intraperitoneal injection and four hybridoma cell lines, which secreted monoclonal antibody(mAb) against human cTnI, were obtained by cell fusion, identification and cloning twice. Three mAbs(9F5, 2F11, 8C12) were produced from the ascites of Balb/c mice injected intraperitoneally the hybridoma cells and characterized by means of a surface plasmon resonance(SPR) biosensor. An optimal and specific sensing membrane for troponin I was prepared with staphylococcal protein A(SPA) as the intermediate layer and mAb against human cTnI as the capture antibody. On the basis of the sensing membrane, two modes of operation of the SPR biosensor were developed, i.e ., a direct detection of antigen antibody affinity and a sandwich assay. In the sandwich assay detection mode, the mAbs competition was measured by monitoring whether the secondary antibody had been attached to the cTnI already captured by the first antibody on the sensor surface. The SPR biosensor was shown to be able to directly detect the antigen antibody affinity and the order of the affinity was found to be 9F5>2F11>8C12. In the sandwich detection mode, it was found that the different epitopes on the cTnI molecules were recognized by the three mAbs respectively, but the asymmetrical competition was shown between 2F11 and 8C12 and no competition was found between 9F5 and 2F11 or 8c12. Based on these results, a double monoclonal sandwich immunoassay for cTnI was developed by using the optimal antibody pair of 9F5 and 2F11 and the SPR biosensor with SPA substrate membrane, which showed an excellent sensitivity of 0.8 μg/L for both the buffer and the serum samples compared with the direct detection of cTnI for the buffer with the lowest detection limit of 4 μg/L and conventional ELISA with the sensitivity of 1.9 μg/L.
