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Immunological evaluation of some antigens of Lucilia sericata larvae

机译:绢丝Luclucata sericata幼虫某些抗原的免疫学评估

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摘要

The present study aimed to select an antigen of Lucilia sericata larvae showing both high antigenicity and cross-reactive binding abilities with other related antigens of L. sericata larvae for obtaining a promising candidate vaccine antigen. The ELISA results primary concluded that among the excretory secretory (ES) and midgut (MG) antigens of the different larval instars of L. sericata, MGL2 could be characterized as antigen which was able to reflect the highest level of antigenicity and cross-reactivity with the other tested L. sericata antigens. The results were extended to spot the light on the relation between different protein bands in MGL2 and rabbit hyper- immune sera (HIS) raised against the other tested antigens using SDS-PAGE and Western blot technique. Analysis by SDS-PAGE of ES and MG antigens of the different larval instars of L. sericata revealed common protein bands at molecular weights of about 10, 12, 16, 20, 28, 33 and 46 kDa. Western blotting of MGL2 antigen transferred to nitrocellulose sheet revealed reaction by MGL2 HIS to five polypeptide bands; 20, 28, 33, 46 and 63 kDa. Three bands of 28, 33 and 63 kDa were the most prominent bands detected whereas; there was a weak reaction with bands of 20 and 46 kDa. But what was apparent in Western blot was a strong reaction of all tested HIS with a polypeptide band of 63 kDa. This band might be considered to be the main cause of cross reactive binding ability of MGL2 antigen that had been recorded previously in ELISA technique.
机译:本研究旨在选择一种能显示出高潜力的候选疫苗抗原的丝状Lucilia sericata幼虫抗原,同时显示出与丝状L. sericata幼虫其他相关抗原的高抗原性和交叉反应结合能力。 ELISA结果的主要结论是,在丝状线虫不同幼龄期的排泄分泌(ES)和中肠(MG)抗原中,MGL2可被表征为能够反映最高水平的抗原性和交叉反应性的抗原。其他测试的丝胶乳杆菌抗原。使用SDS-PAGE和Western blot技术,将结果扩展到将MGL2中不同蛋白条带与针对其他测试抗原产生的兔超免疫血清(HIS)之间的关系聚焦。通过SDS-PAGE分析丝线莲不同幼虫的ES和MG抗原,发现分子量为10、12、16、20、28、33和46 kDa的常见蛋白条带。转移至硝酸纤维素膜的MGL2抗原的Western印迹揭示了MGL2 HIS对五个多肽条带的反应。 20、28、33、46和63 kDa。 28、33和63kDa的三个带是检测到的最突出的带,而; 20和46 kDa的条带反应较弱。但是在Western印迹中显而易见的是,所有测试的HIS与63 kDa的多肽条带都有强烈的反应。该条带可能被认为是先前在ELISA技术中已记录的MGL2抗原交叉反应结合能力的主要原因。

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