Tani iin laboratuvar kriterleri; (1) Destekleyici: Serum orneklerinden
Rose Bengal testi ile antikor pozitifligi; (2) Dogrulayici: Klinik orneklerden Brucella spp.'nin izolasyonu ve/veya daha once tedavi almamis bir olguda tek serum orneginde STA ile antikor titresinin >1:160 olmasi ve/veya en az iki hafta ara ile alinan cift serum orneginde Brucella STA titresinin >4 kat artis olmasidir (8).
The seropositivity of 9.6% using
Rose Bengal Plate Test (RBPT) is higher than that obtained by Ogugua et al., 2014, whose findings revealed an overall seroprevalence of 2.83% of brucellosis among goats screened across four states in Nigeria.
Rose Bengal Plate test (RBPT) and indirect Enzyme-Linked Immunosorbent Assay (i-ELISA) test were performed on a total of 1031 head of cattle from 82 herds (18 villages communities) owned by 52 farmers.
Serum samples were screened initially by
Rose Bengal Plate Test (RBPT) and then confirmed by Serum Agglutination Test (SAT) as described by Alton et al.
RSA antigen was prepared using
Rose Bengal dye and compared with a commercially prepared RSA antigen.
On the other hand, the photochemical properties of various xanthenic dyes, mainly
rose bengal (RB) and eosin (Eo), have been extensively studied due to their diverse applications that derive mainly from their large molar absorption coefficients in the visible region and their high quantum yields of singlet oxygen generation.
That is the case of cyclic anionic xanthene dyes with three aromatic rings in linear arrangement and an atom of oxygen in the central ring as, for example,
Rose Bengal (RB), erythrosin B (EB), eosin Y (EY), and fluorescein (FL) (Figure 1).
PV-10 is an injectable formulation of
Rose Bengal that is under investigation as an ablative immunotherapy for solid tumor cancers.
[6] There are numerous commercial kits and serological methods commonly used and recommended, including the
Rose Bengal test, serum tube agglutination and enzyme-linked immunosorbent assay (ELISA).
Rose Bengal is a fluorescein derivative, which stains dead and damaged cells and mucus with no effect over epithelial defects or intercellular spaces.
Sera from 110 volunteers were collected and analyzed by employing serology (
Rose Bengal Test, competitive ELISA, FPA) and serum PCR assay.