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10.1111/1574-6968.12063 http://scihub22266oqcxt.onion/10.1111/1574-6968.12063 23227897!7108531!23227897     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=23227897&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       FEMS+Microbiol+Lett 2013 ; 340 (2): 86-92 Nephropedia Template TP {{tp|p=23227897|t=2013. Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma pneumoniae infections |pdf=|usr=}}{{23227897}} gab.com Text Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma pneumoniae infections JO: FEMS Microbiol Lett http://www.kidney.de/pget.php?&tw=1&pmid=23227897 #FOAvip Most glycolipid antigens used for serological tests of Mycoplasma pneumoniae are not M. pneumonia-specific, and can cross-react with other microorganism antigens and body tissues, resulting in false positives. It is important to identify M. pneumonia-specific antigen(s) for serological testing and correct diagnosis. Two epitopes, rP1-534 and rP1-513, of P1 adhesin predicted by bioinformatics were successfully expressed and purified, and could be recognized by serum samples from M. pneumoniae-infected patients and His tag antibodies by Western blot. There was no cross-reactivity between the anti-recombinant proteins serum and other respiratory antigens. A total of 400 patients were investigated, their respiratory specimens tested by PCR, and sera tested by a commercial test kit; 56 with positive sera and positive respiratory specimens were designated as standard positive serum and 63 patients were designated as standard negative serum. The purified recombinant proteins were used as a combination of antigens or separately to test the serum. Serological test demonstrated that rP1-513 of the C terminal of P1 adhesin is a new candidate antigen with greater sensitivity and specificity for IgG and IgM serodiagnosis of M. pneumoniae-infected patients. The results confirmed that rP1-513 could be a useful new antigen for the immunodiagnosis of M. pneumoniae infection. Twit Text FOAVip Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma pneumoniae infections ????FEMS Microbiol Lett http://www.kidney.de/pget.php?&tw=1&pmid=23227897 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=23227897 #FOAvip English Wikipedia <ref>{{Cite pmid|23227897}}</ref> Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma pneumoniae infections #MMPMID23227897 Xue G; Cao L; Wang L; Zhao H; Feng Y; Ma L; Sun H FEMS Microbiol Lett 2013[Mar]; 340 (2): 86-92 PMID23227897show ga Most glycolipid antigens used for serological tests of Mycoplasma pneumoniae are not M. pneumonia-specific, and can cross-react with other microorganism antigens and body tissues, resulting in false positives. It is important to identify M. pneumonia-specific antigen(s) for serological testing and correct diagnosis. Two epitopes, rP1-534 and rP1-513, of P1 adhesin predicted by bioinformatics were successfully expressed and purified, and could be recognized by serum samples from M. pneumoniae-infected patients and His tag antibodies by Western blot. There was no cross-reactivity between the anti-recombinant proteins serum and other respiratory antigens. A total of 400 patients were investigated, their respiratory specimens tested by PCR, and sera tested by a commercial test kit; 56 with positive sera and positive respiratory specimens were designated as standard positive serum and 63 patients were designated as standard negative serum. The purified recombinant proteins were used as a combination of antigens or separately to test the serum. Serological test demonstrated that rP1-513 of the C terminal of P1 adhesin is a new candidate antigen with greater sensitivity and specificity for IgG and IgM serodiagnosis of M. pneumoniae-infected patients. The results confirmed that rP1-513 could be a useful new antigen for the immunodiagnosis of M. pneumoniae infection. |Adhesins, Bacterial/genetics/*immunology[MESH] |Adolescent[MESH] |Animals[MESH] |Antibodies, Bacterial/immunology[MESH] |Child[MESH] |Child, Preschool[MESH] |Cross Reactions[MESH] |Epitopes/genetics/immunology[MESH] |Female[MESH] |Humans[MESH] |Male[MESH] |Mice[MESH] |Mice, Inbred BALB C[MESH] |Mycoplasma pneumoniae/genetics/immunology/*physiology[MESH] |Pneumonia, Mycoplasma/*diagnosis/immunology/microbiology[MESH]Evaluation of P1 adhesin epitopes for the serodiagnosis of Mycoplasma (epmc).pdf DeepDyve Pubget Overpricing