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2 system for the detection of M. tuberculosis alpha-antigen (85B protein) mRNA and to demonstrate the
3 els of 16S rRNA, fbpB mRNA (encoding the 85B alpha antigen), and aroB mRNA (encoding dehydroquinate s
5 cells were negative for CD34, CD14, and CD8 alpha antigens but expressed low levels of the myeloid m
8 sly cloned, sequenced, and characterized the alpha antigen gene, bca, and showed that the alpha C pro
10 r allowed a simple and fast detection of TNF alpha antigen in human serum and satisfied recoveries (9
11 monstrated cytoplasmic staining for the CD79 alpha antigen, including one M1, nine M3, and one M5 AML
12 first 24 h, suggesting that the role of the alpha antigen is important in the initial stages of the
14 Levels of mRNA encoding the 85B protein (alpha-antigen), IS6110 DNA, and 16S rRNA were compared i
15 , we measured levels of M. tuberculosis 85B (alpha antigen) messenger RNA (mRNA), 16S ribosomal RNA (
16 or to the start of therapy were positive for alpha-antigen mRNA, compared with 1 of 8 (13%), 2 of 8 (
18 oxidation of catechol, determination of TNF-alpha antigen was based on its obstruction to the electr
20 tion between anti-TNF alpha antibody and TNF alpha antigen were monitored by cyclic voltammetry (CV)
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