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Alexa fluor 488 conjugated goat anti human igg antibody

Manufactured by Thermo Fisher Scientific
Sourced in United States

Alexa Fluor 488-conjugated goat anti-human IgG antibody is a secondary antibody that binds to human immunoglobulin G (IgG) antibodies. The antibody is labeled with the Alexa Fluor 488 fluorescent dye, which can be excited at 488 nm and emits green fluorescence. This product is commonly used in immunofluorescence and flow cytometry applications.

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2 protocols using alexa fluor 488 conjugated goat anti human igg antibody

1

Immunofluorescence Assay for Influenza Virus

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MDCK cells (96 well plate format, 5 × 104 cells/well, triplicates) were inoculated with Brisbane/H1N1, pH1N1, NC/H1N1, PR8/H1N1, WI/H1N1, GA/H1N1, and Brisbane/H3N2 at multiplicity of infection (MOI) of 10, or mock infected. At 8 h post-infection (p.i.), cells were fixed with 10% neutral buffered formalin (NBF; Thermo Fisher Scientific, CA, USA) for 1 h and then stained with 1 μg/mL of KPF1-HEK or KPF1-Antx hMAbs, followed by secondary Alexa Fluor 488-conjugated goat anti-human IgG antibody (Life Technologies, Carlsbad, CA, USA). DAPI (4’,6-diamidino-2-phenylindole, Thermo Fisher Scientific, CA, USA) was used to stain cell nuclei. Fluorescent signal images were acquired under an inverted fluorescent microscope (Olympus, Japan) and analyzed by ImageJ software to measure intensity of the staining (NIH, Bethesda, MD, USA) [53 (link)].
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2

MDCK Cell Influenza Viral Infection Assay

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MDCK cells (96 well plate format, 5 x 10 4 cells/well, triplicates) were inoculated with Brisbane/H1N1, pH1N1, NC/H1N1, PR8/H1N1, WI/H1N1, GA/H1N1, and Brisbane/H3N2 at multiplicity of infection (MOI) of 10, or mock infected. At 8 h postinfection (p.i.), cells were fixed with 10% neutral buffered formalin (NBF; Thermo Fisher Scientific, CA, USA) for 1 h and then stained with 1 μg/ml of KPF1-HEK or KPF1-Antx hMAbs, followed by secondary Alexa Fluor 488-conjugated goat anti-human IgG antibody (Life Technologies, Carlsbad, CA, USA). DAPI (4',6-diamidino-2-phenylindole, Thermo Fisher Scientific, CA, USA) was used to stain cell nuclei. Fluorescent signal images were acquired under an inverted fluorescent microscope (Olympus, Japan) and analyzed by ImageJ software to measure intensity of the staining (NIH, Bethesda, MD, USA) [54] .
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