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A647 donkey anti rabbit igg

Manufactured by Thermo Fisher Scientific

The A647 Donkey anti-Rabbit IgG is a secondary antibody that binds to rabbit primary antibodies. It is conjugated with the Alexa Fluor 647 fluorescent dye, which can be detected using appropriate instrumentation.

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2 protocols using a647 donkey anti rabbit igg

1

Immunophenotyping of Blood Cells

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Pipette blood samples into 1.5 mL EP tubes. Spin at 4°C for 10 minutes at 300g, then discard the supernatant. Add 200 μL of PBS/0.5% BSA and vortex. Next, incubate for 10 minutes with primary antibodies at 4°C. Spin at 4°C for 10 minutes at 300g, discard the supernatant, and add 200 μL of PBS/0.5% BSA. Incubate for 10 minutes with fluorescent-labeled secondary antibodies and DAPI at 4°C. Spin at 4°C for 10 minutes at 300g, discard the supernatant, and smear. Seal the slices with an anti-fluorescence quencher. Immunofluorescent images were captured using the fluorescence microscope (Leica DMI300B). The fluorescent intensity was acquired using the software ImageJ. The primary antibodies used in this study include: Rat-anti-human CD19 (Invitrogen, #11-0193-82), Mouse-anti-human CD27 (Sigma-Aldrich, #SAB4700131), Rabbit-anti-human MIF (Affinity, #DF6404), Mouse-anti-human CD68 (Invitrogen, #14-0688-82), Rat-anti-human CD44 (Invitrogen, #14-0441-82), and Goat-anti-human CD74 (Invitrogen, #PA5-143198). The secondary antibodies used in this study include: A594 Goat Anti-Rabbit IgG (Affinity, #S0006), A647 Goat Anti-Mouse IgG (Bi Yuntian, #A0473), A488 Donkey-anti-Mouse IgG (Invitrogen, #A21202), A647 Donkey anti-Rabbit IgG (Invitrogen, #A32795), and DAPI (Invitrogen, #D1306).
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2

Immunofluorescent Profiling of Cervical Cancer

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Biopsies were taken from six cervical patients with cervical cancer. After embedding with a frozen section compound (Leica, #3801480), biopsies were sectioned into 4-μm on a microtome (Leica CM1950). For immunofluorescent staining, the sections were fixed in pre-cooled methanol (-20°C) for 5 minutes, after washing twice with PBS. The sections were then blocked with PBS/5%BSA/Fcγ blocker at 4°C for 1 hour. Primary antibodies were incubated with sections at 4°C overnight. After washing twice with PBS, the sections were incubated with fluorescent-coupled secondary antibodies for 1 hour at room temperature. After two further washes, the sections were mounted and imaged on an immunofluorescence microscope (Leica DMI3000B).
The antibodies/materials used for immunofluorescent imaging included: A488 mouse-anti-human CD206 (Invitrogen, #MA5-23656), PE mouse-anti-human CD163 (Invitrogen, #12-1639-42), A488 mouse-anti-human EpCam (Abcam, #ab237395), mouse-anti-human KRT16/Cytokeratin Pan Antibody Cocktail (Invitrogen, #MA5-13203), rabbit-anti-human CRCT1 (Invitrogen, #PA5-23539), A594 goat-anti-mouse IgG (Invitrogen, #A11032), A594, goat-anti-rabbit IgG (Affinity, #S0006), rabbit-anti-human DR5 (Invitrogen, # PA1-957), A647 donkey-anti-rabbit IgG (Invitrogen, #A32795) and DAPI (Invitrogen, #D21490).
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