polyclonal rabbit anti vacv le antibody  (OriGene)

Journal: PLoS ONE

Article Title: Development of a Genus-Specific Antigen Capture ELISA for Orthopoxviruses – Target Selection and Optimized Screening

doi: 10.1371/journal.pone.0150110

Figure Lengend Snippet: A . Conservation of immunogenic epitopes of recombinant proteins was verified through the recognition of immobilized surface proteins by vaccinia immunoglobulin (VIG) employing an indirect ELISA. Lysates from vaccinia virus infected (VACV NYCBOH ) or non-infected HEp-2 cells were used as the positive or negative control. B . The reactivity of anti-A27, -L1, -D8 and -H3 antibodies (1:1000) against VACV-infected (strain NYCBOH) or non-infected (n-) HEp-2 cells (40 μg lysate per lane) by western immunoblotting. HRP-labelled goat anti-rabbit or rabbit anti-goat IgG antibodies (1:5000) were used for detection. C . Percentage of plaque reduction (PRNT; ranging from 0% to 100%) for two-fold serial dilutions of anti-A27, -L1, -D8 and -H3 antibodies. VIG was included as the positive control. D . IFA of VACV LE infected Hep-2 cells with different combinations of polyclonal antibodies targeting surface proteins (A27, L1, D8 and H3) or vaccinia virus (VACV). Compared to the other antibodies, for the analysis of anti-H3 stained infected cells, the detector gain had to be increased due to the lower signal intensity. Antibodies were either stained with species-specific FITC-labelled secondary antibodies (green) or labeled directly with DyLight 649 (red). Cell nuclei were counterstained with DAPI (blue). Scale bar = 100 μm.

Article Snippet: A polyclonal rabbit anti-VACV LE antibody was obtained from Acris Antibodies (Herford, Germany).

Techniques: Recombinant, Indirect ELISA, Virus, Infection, Negative Control, Western Blot, Positive Control, Staining, Labeling

Journal: PLoS ONE

Article Title: Development of a Genus-Specific Antigen Capture ELISA for Orthopoxviruses – Target Selection and Optimized Screening

doi: 10.1371/journal.pone.0150110

Figure Lengend Snippet: A . Immobilized recombinant proteins or purified UV-inactivated VACV NYCBOH particles were incubated with a dilution series of purified biotinylated anti-A27, -D8, -H3 and -L1 antibodies in an indirect ELISA. Detection was done with SA-pHRP (1:5000). B . Representative electron microscopic pictures of anti-A27, -D8, or -H3 antibodies binding to purified VACV NYCBOH . Biotinylated antibodies were detected using 5 nm immunogold labelled streptavidin. Scale bars = 100 nm. C . Box-and-whisker plot for quantification of the number of gold particles per viral particle (whiskers: min to max; A27 n = 111; D8 n = 109 viral particles analyzed).

Article Snippet: A polyclonal rabbit anti-VACV LE antibody was obtained from Acris Antibodies (Herford, Germany).

Techniques: Recombinant, Purification, Incubation, Indirect ELISA, Binding Assay, Whisker Assay

Journal: PLoS ONE

Article Title: Development of a Genus-Specific Antigen Capture ELISA for Orthopoxviruses – Target Selection and Optimized Screening

doi: 10.1371/journal.pone.0150110

Figure Lengend Snippet: A . Binding epitopes and multiple sequence alignment (NCBI BLink) of different OPV strains. Identical sequences with the prominent strain are denoted in brackets, followed by the number of identical sequences deposited in GenBank. The binding epitopes for mAb A3/710 from amino acid 13 to 27 (A) and all other anti-A27 mAbs from amino acid 24 to 38 (B) border the heparin binding site (HBS) on A27. Both the VACV NYCBOH strain and E . coli derived A27 based on CPXV calpox DNA show 100% sequence identity with the reference strain VACV WR in this region. B . Compatibility of all eight anti-A27 mAbs for antigen capture ELISA. All possible combinations of coating antibodies (x-axis) and biotinylated detection were paired and tested for the detection of 5×10 6 PFU/ml UV-inactivated VACV NYCBOH . Shown are representative results for the highest virus concentration tested. The results from the titration series are shown in . C . SPR sensorgrams to determine the binding kinetics of anti-A27 mAbs. Measured responses (double referenced resonance units RU; difference between flow cell 2 minus flow cell 1) are shown as red lines whereas black lines represent results from fitting a 1:1 Langmuir interaction.

Article Snippet: A polyclonal rabbit anti-VACV LE antibody was obtained from Acris Antibodies (Herford, Germany).

Techniques: Binding Assay, Sequencing, Derivative Assay, Enzyme-linked Immunosorbent Assay, Virus, Concentration Assay, Titration

Journal: PLoS ONE

Article Title: Development of a Genus-Specific Antigen Capture ELISA for Orthopoxviruses – Target Selection and Optimized Screening

doi: 10.1371/journal.pone.0150110

Figure Lengend Snippet: A . Titration curve of rA27 with the antigen capture ELISA. B . To check for cross-reactivity, PPXV, HSV-1 and tanapox virus were tested. C . Detection of different VACV strains by the newly developed assay. D . Detection of different OPV.

Article Snippet: A polyclonal rabbit anti-VACV LE antibody was obtained from Acris Antibodies (Herford, Germany).

Techniques: Titration, Enzyme-linked Immunosorbent Assay, Virus

Journal: PLoS ONE

Article Title: Development of a Genus-Specific Antigen Capture ELISA for Orthopoxviruses – Target Selection and Optimized Screening

doi: 10.1371/journal.pone.0150110

Figure Lengend Snippet: Limits of detection (LOD) of the newly developed A27-specific antigen sandwich ELISA for different OPV strains.

Article Snippet: A polyclonal rabbit anti-VACV LE antibody was obtained from Acris Antibodies (Herford, Germany).

Techniques: Sandwich ELISA