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Alexa fluor 488 conjugated goat anti chicken igg antibody

Manufactured by Thermo Fisher Scientific

The Alexa Fluor 488-conjugated goat anti-chicken IgG antibody is a fluorescently labeled secondary antibody. It is designed to detect and bind to chicken immunoglobulin G (IgG) antibodies in various immunoassay applications.

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

1

Whole-Mount Immunofluorescence Staining of Zebrafish Embryos

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Embryos and larvae were fixed in 4% PFA (pH 7.3) over night at 4 °C and stored in PBS containing 0.1% Tween 20 at 4 °C until use. WIF experiments were performed essentially as described33 (link) using the following antibodies: rabbit anti-T4 polyclonal antibody (1:2000; MP Biochemicals), chicken anti-GFP polyclonal antibody (1:1000; Abcam), rabbit anti-pax2a polyclonal antibody (1:250; GeneTex), cy3-conjugated donkey anti-rabbit IgG antibody (1:250; Jackson ImmunoResearch), and Alexa Fluor 488-conjugated goat anti-chicken IgG antibody (1:250; Invitrogen). Stained specimens were postfixed in 4% PFA, gradually transferred to 100% glycerol and phenotypically analysed using a M165 FC fluorescence stereomicroscope. Whole mount imaging of stained specimens was performed with a DMI600B epifluorescence microscope equipped with a DFC365FX camera.
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2

Immunohistochemistry for GFP and reporter proteins

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Tissue was isolated, fixed, sectioned, and permeabilized as described above. Tissue was blocked in 10% normal goat serum in PBS for 1 h, followed by an overnight incubation at 4°C with chicken polyclonal anti-GFP (1:2500 dilution; catalog 13970; Abcam). Following washes, sections were incubated with Alexa Fluor-488-conjugated goat anti-chicken IgG antibody (1:2000 dilution; Invitrogen) for 2 h. No antibody amplification was necessary for the tTA::miR-212 dsRED signal. Sections were also incubated for 10 min with the nuclear stain DRAQ5 (1:10,000 dilution; BioStatus Limited, UK and Hoechst 33258 (1:1000 dilution: Sigma), followed by an additional three 10-min washes. Sections were mounted on slides with Fluoromount-G (SouthernBiotech) and images captured using a 16-bit digital camera (Micromax YHS 1300; Princeton Instruments) mounted on an inverted Leica microscope (DM IRB).
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