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Development of a Highly Specific IgM Enzyme Linked Immunosorbent Assay for Bartonella henselae Using Refined N Lauroyl Sarcosine Insoluble Proteins for Serodiagnosis of Cat Scratch Disease

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Academic year: 2020

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Figure

FIG 1 The flow diagram for preparation of antigen I to V.vested from the agar medium was sonicated and treated with sarcosine
FIG 2 The reactivity of fractions from DEAE-Sepharose to anti-B. henselae IgM antibody
FIG 3 SDS-PAGE and Western blot analyses of 5 proteins associated withproteins; R-ins, sarcosine-insoluble proteins refined by DEAE-Sepharose chromatography; R-sol, sarcosine-soluble proteins refined by DEAE-Sepharose chro-matography
TABLE 2 The detailed test results of the 24 cases of cat scratch diseasewhich were proven by IgG-IFA, IgM-IFA, or PCRa

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