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influenza virus nucleoprotein  (Novus Biologicals)
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Novus Biologicals influenza virus nucleoprotein
Viral genomes were sequenced and the translated amino acid sequence of the polymerase basic (A), hemagglutinin (B), <t>nucleoprotein</t> (C) and neuraminidase (D) are illustrated. 10 clones from each virus and each gene segment were submitted for sequencing. Heterogeneity in the sequence was observed and designated as CA/07.1 and CA/07.2 or NL/602.1 or NL/602.2 with the dominant sequence designated as CA/07.1 or NL/602.1. The consensus amino acid sequences are shown. Identical residues are depicted as dots and differences in amino acid sequence are shown.
Influenza Virus Nucleoprotein, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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influenza virus nucleoprotein - by Bioz Stars, 2026-04
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Viral genomes were sequenced and the translated amino acid sequence of the polymerase basic (A), hemagglutinin (B), nucleoprotein (C) and neuraminidase (D) are illustrated. 10 clones from each virus and each gene segment were submitted for sequencing. Heterogeneity in the sequence was observed and designated as CA/07.1 and CA/07.2 or NL/602.1 or NL/602.2 with the dominant sequence designated as CA/07.1 or NL/602.1. The consensus amino acid sequences are shown. Identical residues are depicted as dots and differences in amino acid sequence are shown.

Journal: PLoS ONE

Article Title: Closely Related Influenza Viruses Induce Contrasting Respiratory Tract Immunopathology

doi: 10.1371/journal.pone.0076708

Figure Lengend Snippet: Viral genomes were sequenced and the translated amino acid sequence of the polymerase basic (A), hemagglutinin (B), nucleoprotein (C) and neuraminidase (D) are illustrated. 10 clones from each virus and each gene segment were submitted for sequencing. Heterogeneity in the sequence was observed and designated as CA/07.1 and CA/07.2 or NL/602.1 or NL/602.2 with the dominant sequence designated as CA/07.1 or NL/602.1. The consensus amino acid sequences are shown. Identical residues are depicted as dots and differences in amino acid sequence are shown.

Article Snippet: Tissues were incubated with rabbit polyclonal antibodies specific to influenza virus nucleoprotein (Novus Biologicals, Littleton, CO) anti-CD11b-PE (Becton Dickinson Biosciences, San Jose, CA) and anti-F4/80- biotin (eBiosciences, San Diego, CA) followed by incubation with goat anti-rabbit-horseradish peroxidase (Southern Biotechnologies, Birmingham, AL), streptavidin-Alexa fluor 647 and tyramide signal amplification (Life Technologies).

Techniques: Sequencing, Clone Assay, Virus

Frozen lung sections collected two (B) and four (C) days post infection were stained with anti-influenza nucleoprotein (blue), anti-F4/80 antigen (green) or anti-CD11b (red). Both CA/07 and NL/602 induced expression of viral nucleoprotein prominently on bronchiole epithelial cells and modest expression on alveolar epithelial cells. F4/80 + and CD11b + cells were detected in greater abundance upon infection with NL/602 compared to naïve lung. In contrast, CA/07 infection yielded substantially greater recruitment of CD11b + cells while F4/80 + cells were minimally detected. Insets from CA/07 and NL/602 shown in 40X objective (D). Scale bars represent 100µm.

Journal: PLoS ONE

Article Title: Closely Related Influenza Viruses Induce Contrasting Respiratory Tract Immunopathology

doi: 10.1371/journal.pone.0076708

Figure Lengend Snippet: Frozen lung sections collected two (B) and four (C) days post infection were stained with anti-influenza nucleoprotein (blue), anti-F4/80 antigen (green) or anti-CD11b (red). Both CA/07 and NL/602 induced expression of viral nucleoprotein prominently on bronchiole epithelial cells and modest expression on alveolar epithelial cells. F4/80 + and CD11b + cells were detected in greater abundance upon infection with NL/602 compared to naïve lung. In contrast, CA/07 infection yielded substantially greater recruitment of CD11b + cells while F4/80 + cells were minimally detected. Insets from CA/07 and NL/602 shown in 40X objective (D). Scale bars represent 100µm.

Article Snippet: Tissues were incubated with rabbit polyclonal antibodies specific to influenza virus nucleoprotein (Novus Biologicals, Littleton, CO) anti-CD11b-PE (Becton Dickinson Biosciences, San Jose, CA) and anti-F4/80- biotin (eBiosciences, San Diego, CA) followed by incubation with goat anti-rabbit-horseradish peroxidase (Southern Biotechnologies, Birmingham, AL), streptavidin-Alexa fluor 647 and tyramide signal amplification (Life Technologies).

Techniques: Infection, Staining, Expressing