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The minor core protein s C-encoding gene of Muscovy duck reovirus was cloned into theprokaryotic expression vector pET32a. The recombinant plasmid pET32a-s C was amplified andextracted after being transformed into E.coli DH5a competent cells. Restriction analysis withEcoRⅠand SacⅠand sequences analysis indicated that the recombinant plasmid was inserted withcorrect open reading frame. The fusion protein about 50 ku was produced after induction with 0.15mmol/L IPTG of E.coli competent cells transformed with pET32a-sC. The SDS-PAGE andWestern-bloting test indicated that the fusion protein reacted with the convalescents sera of duckinfected with Muscovy duck reovirus. The indirect ELISA method was developed by using thepurified fusion s C protein as coating antigen. The optimal concentration of s C was 5μg/ml, thedilution of serum sample was 1:40; The results showed that preparation of an ELISA by using sCas coating antigen in detecting 50 field duck sera in comparison with the AGIP were more sensitiveand specific than agar gel immuno-diffusion AGIP test. The results suggest that presence ofantibody against viral protein sC in duck may be a good indicator by the sC-ELISA for detectionof duck infection with reovirus.

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In order to making an initial statistical research for the AGNs evolution, we investigated the distribution of the redshift and the spectral index and the flux densities in different wavebands.

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Pregnant adult C 57 BL/6 J strain mice, randomly assigned to 1 of4 experimental groups, were irradiated with exponentially decreasing doses of tritiumbeta-rays but group 1 by single injection of tritiated water at their 12.5 th day of gestation.

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Put champions in your side of th ri ng s – champions like Bl nnPR's dedicated and h h Smart y ex perienced senior level PR pt rofessi Vehicle als – and you'll come out on top.

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