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Novus Biologicals agalactiae monoclonal antibody
Fig. 1. Antibodies raised in mice immunized with rBibA bind to the native protein exposed on the surface of GBS cells of different serotypes. (A) Whole-cell ELISA performed with GBS cells belonging to different serotypes and serum samples collected 2 weeks after the third immunization with rBibA admixed with alum. Values represent the mean ± SD. Significant differences between groups were determined using two-way ANOVA with Tukey’s post hoc test. ****p < 0.0001, ***p < 0.001, and *p < 0.05; ns: nonsignificant. (B) Immunofluorescence detection of GBS-V using antibodies raised in BALB/c mice immunized with rBibA. Tested antibodies: i) anti-S. <t>agalactiae</t> <t>monoclonal</t> antibody (mAb 224/46) (Novus Biologicals), ii) polyclonal serum raised against whole inactivated GBS-V (anti-GBS-V), iii) serum samples from mice immunized with rBibA- alum (anti-BibA), and iv) serum samples collected from saline-treated mice (non-immune serum). Cells were evaluated on an AMG EVOS flLED fluorescence microscope at a magnification of 40. Scale bar: 100 mm. The columns show transmitted light (left), GFP fluorescence (center) and merged images (right). Red arrows point GBS-V cells detected by the indicated antibody. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
Agalactiae Monoclonal Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Fig. 1. Antibodies raised in mice immunized with rBibA bind to the native protein exposed on the surface of GBS cells of different serotypes. (A) Whole-cell ELISA performed with GBS cells belonging to different serotypes and serum samples collected 2 weeks after the third immunization with rBibA admixed with alum. Values represent the mean ± SD. Significant differences between groups were determined using two-way ANOVA with Tukey’s post hoc test. ****p < 0.0001, ***p < 0.001, and *p < 0.05; ns: nonsignificant. (B) Immunofluorescence detection of GBS-V using antibodies raised in BALB/c mice immunized with rBibA. Tested antibodies: i) anti-S. agalactiae monoclonal antibody (mAb 224/46) (Novus Biologicals), ii) polyclonal serum raised against whole inactivated GBS-V (anti-GBS-V), iii) serum samples from mice immunized with rBibA- alum (anti-BibA), and iv) serum samples collected from saline-treated mice (non-immune serum). Cells were evaluated on an AMG EVOS flLED fluorescence microscope at a magnification of 40. Scale bar: 100 mm. The columns show transmitted light (left), GFP fluorescence (center) and merged images (right). Red arrows point GBS-V cells detected by the indicated antibody. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

Journal: Vaccine

Article Title: Immunization with a recombinant BibA surface protein confers immunity and protects mice against group B Streptococcus (GBS) vaginal colonization.

doi: 10.1016/j.vaccine.2020.05.076

Figure Lengend Snippet: Fig. 1. Antibodies raised in mice immunized with rBibA bind to the native protein exposed on the surface of GBS cells of different serotypes. (A) Whole-cell ELISA performed with GBS cells belonging to different serotypes and serum samples collected 2 weeks after the third immunization with rBibA admixed with alum. Values represent the mean ± SD. Significant differences between groups were determined using two-way ANOVA with Tukey’s post hoc test. ****p < 0.0001, ***p < 0.001, and *p < 0.05; ns: nonsignificant. (B) Immunofluorescence detection of GBS-V using antibodies raised in BALB/c mice immunized with rBibA. Tested antibodies: i) anti-S. agalactiae monoclonal antibody (mAb 224/46) (Novus Biologicals), ii) polyclonal serum raised against whole inactivated GBS-V (anti-GBS-V), iii) serum samples from mice immunized with rBibA- alum (anti-BibA), and iv) serum samples collected from saline-treated mice (non-immune serum). Cells were evaluated on an AMG EVOS flLED fluorescence microscope at a magnification of 40. Scale bar: 100 mm. The columns show transmitted light (left), GFP fluorescence (center) and merged images (right). Red arrows point GBS-V cells detected by the indicated antibody. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

Article Snippet: The wells were incubated with the following primary antibodies: i) anti-S. agalactiae monoclonal antibody (224/46) (1:100) (Novus Biologicals), ii) polyclonal serum raised against GBS-V (1:50), iii) polyclonal serum raised against BibA-alum (1:50), and iv) control serum raised against saline (1:50).

Techniques: Enzyme-linked Immunosorbent Assay, Saline, Microscopy