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fluorescein fitc conjugated avidin  (Vector Laboratories)


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    Structured Review

    Vector Laboratories fluorescein fitc conjugated avidin
    Fluorescein Fitc Conjugated Avidin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 412 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fluorescein fitc conjugated avidin/product/Vector Laboratories
    Average 95 stars, based on 412 article reviews
    fluorescein fitc conjugated avidin - by Bioz Stars, 2026-06
    95/100 stars

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    95
    Vector Laboratories fitc conjugated avidin
    U/R cells were infected with the 1xMycR virus and analyzed by immunofluorescence, as described in . p12 (A–C), MA(A, B) and CA (C) were detected with the anti-Myc monoclonal antibody, goat anti-MA and goat anti-CA polyclonal antibodies, respectively, and the matched <t>secondary</t> <t>FITC-conjugated</t> donkey anti-mouse IgG and Red-X- conjugated donkey anti-goat IgG. For consistency, the images were pseudocolored to present p12 in red and MA or CA in green. Dashed lines mark the boundaries of cell-free regions where virions were detected attached to the cover glass. Bars represent 10 µm.
    Fitc Conjugated Avidin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    U/R cells were infected with the 1xMycR virus and analyzed by immunofluorescence, as described in . p12 (A–C), MA(A, B) and CA (C) were detected with the anti-Myc monoclonal antibody, goat anti-MA and goat anti-CA polyclonal antibodies, respectively, and the matched secondary FITC-conjugated donkey anti-mouse IgG and Red-X- conjugated donkey anti-goat IgG. For consistency, the images were pseudocolored to present p12 in red and MA or CA in green. Dashed lines mark the boundaries of cell-free regions where virions were detected attached to the cover glass. Bars represent 10 µm.

    Journal: PLoS Pathogens

    Article Title: The Gag Cleavage Product, p12, is a Functional Constituent of the Murine Leukemia Virus Pre-Integration Complex

    doi: 10.1371/journal.ppat.1001183

    Figure Lengend Snippet: U/R cells were infected with the 1xMycR virus and analyzed by immunofluorescence, as described in . p12 (A–C), MA(A, B) and CA (C) were detected with the anti-Myc monoclonal antibody, goat anti-MA and goat anti-CA polyclonal antibodies, respectively, and the matched secondary FITC-conjugated donkey anti-mouse IgG and Red-X- conjugated donkey anti-goat IgG. For consistency, the images were pseudocolored to present p12 in red and MA or CA in green. Dashed lines mark the boundaries of cell-free regions where virions were detected attached to the cover glass. Bars represent 10 µm.

    Article Snippet: The hybridized biotin-labeled probe was detected with FITC-conjugated avidin (A-2011, Vector Laboratories,1∶400 dilution), which was incubated with the slides for 30 min at 37°C in 1% BSA/4xSSC and 0.1% Tween 20.

    Techniques: Infection, Immunofluorescence

    U/R cells (A–H) or U20S (I) were infected with 1xMycR (A–G, I) or wt (H) viruses, and 12 h (A–E, G–I) or 2 h (F) postinfection the cells were processed for immunofluorescence and FISH analysis. Myc-labeled p12 proteins were detected with a primary anti-Myc monoclonal antibody (A–F, H–I) and a secondary Cy-3-conjugated anti-mouse antibody (A–I). The immunodetection in G was performed with only the secondary, but not the primary, antibodies. The genomic DNA was detected with MLV-derived biotin-labeled probes and a FITC-conjugated avidin (A–I). D and E are magnifications of the insets in A and B, respectively. Arrows indicate overlaps between the viral p12 proteins and the genomic DNA signals. Ellipses and triangles show non-overlapping signals of the p12 and the genomic DNA, respectively. Images A, B, D, E and G–I were taken with a BX50 microscope (Olympus) or with a LSM 510 META confocal microscope (Zeiss) (C and F). Bars represent 10 µm.

    Journal: PLoS Pathogens

    Article Title: The Gag Cleavage Product, p12, is a Functional Constituent of the Murine Leukemia Virus Pre-Integration Complex

    doi: 10.1371/journal.ppat.1001183

    Figure Lengend Snippet: U/R cells (A–H) or U20S (I) were infected with 1xMycR (A–G, I) or wt (H) viruses, and 12 h (A–E, G–I) or 2 h (F) postinfection the cells were processed for immunofluorescence and FISH analysis. Myc-labeled p12 proteins were detected with a primary anti-Myc monoclonal antibody (A–F, H–I) and a secondary Cy-3-conjugated anti-mouse antibody (A–I). The immunodetection in G was performed with only the secondary, but not the primary, antibodies. The genomic DNA was detected with MLV-derived biotin-labeled probes and a FITC-conjugated avidin (A–I). D and E are magnifications of the insets in A and B, respectively. Arrows indicate overlaps between the viral p12 proteins and the genomic DNA signals. Ellipses and triangles show non-overlapping signals of the p12 and the genomic DNA, respectively. Images A, B, D, E and G–I were taken with a BX50 microscope (Olympus) or with a LSM 510 META confocal microscope (Zeiss) (C and F). Bars represent 10 µm.

    Article Snippet: The hybridized biotin-labeled probe was detected with FITC-conjugated avidin (A-2011, Vector Laboratories,1∶400 dilution), which was incubated with the slides for 30 min at 37°C in 1% BSA/4xSSC and 0.1% Tween 20.

    Techniques: Infection, Immunofluorescence, Labeling, Immunodetection, Derivative Assay, Avidin-Biotin Assay, Microscopy