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Ifkine green donkey anti mouse igg

Manufactured by Abbkine
Sourced in China, United States

IFKine™ Green donkey anti-mouse IgG is a secondary antibody conjugated with a green fluorescent dye. It is designed for the detection of mouse primary antibodies in immunofluorescence applications.

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2 protocols using ifkine green donkey anti mouse igg

1

Spinal Cord Immunofluorescence at 3 dpi

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For immunofluorescence of the spinal cord tissues at 3 dpi, tissue slides and round coverslips were blocked with 5% bovine serum albumin for 1 hour, and then incubated with primary antibody overnight at 4°C. The primary antibodies included mouse anti-platelet-derived growth factor receptor (Pdgfr; 1:250; Cat# ab69506; Abcam), mouse anti-caspase 1 (1:250, Cat# sc-398715, Santa Cruz Biotechnology, Santa Cruz, CA, USA), rabbit anti-Nod1 (1:200; Cat# PA5-79747; Invitrogen, Carlsbad, CA, USA), and rabbit anti-CD31 (1:200; Cat# ab24590; Abcam). After washing with PBS three times, the tissues were incubated with the corresponding secondary antibody (IFKine™ Green donkey anti-mouse IgG, 1:300, Cat# A24211, Abbkine, Wuhan, China; Dylight 594, rabbit anti-goat IgG, 1:300, Cat# A23430, Abbkine) for 1 hour at room temperature in the dark. Subsequently, the tissues were stained with 4′,6-diamidino-2-phenylindole (DAPI) for 15 minutes, and images were acquired using fluorescence microscopy (Olympus).
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2

Immunofluorescence Analysis of Autophagy Markers

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Tissue sections were fixed with 4% paraformaldehyde (PFA), permeabilized with 0.3% Triton X-100 for 30 min. Sections were washed three times with PBS, blocked with 10% normal goat serum and incubation with the following primary antibodies at 4°C overnight: anti-LC3II (Cell Signaling Technology, United States) and anti-LAMP1 (Santa Cruz Biotechnology, United States). The next day, they were incubated with Goat anti-Rabbit IgG (H + L) Cross-Adsorbed Secondary Antibody, Alexa Fluor 594 (Thermo Fisher, United States) and IFKine Green Donkey Anti-Mouse IgG (Abbkine, China) for 1 h at 37°C, and treated with DAPI for 10 min. The sections were viewed by an inverted microscope.
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