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Anti ly 6g rb6 8c5

Manufactured by Thermo Fisher Scientific
Sourced in United States

Anti-Ly-6G (RB6-8C5) is a monoclonal antibody that recognizes the Ly-6G antigen, which is specifically expressed on the surface of mouse neutrophils. This antibody is commonly used in flow cytometry and other immunological applications to identify and study neutrophil populations.

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2 protocols using anti ly 6g rb6 8c5

1

Multiparameter Flow Cytometry of Immune Cell Subsets

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Eight-color flow cytometry was conducted using total mononuclear cell preparations and was run on the MACSQuant Analyzer (Miltenyi, Auburn, CA). Antibodies purchased from eBioscience are as follows: anti-CD11b (M1/70); anti-CD18 (M18/2); anti-Ly-6G (RB6-8C5); anti-CD22 (2D6); anti-CD69 (H1.2F3); anti-MHC II (M5/114.15.2); anti-TCRβ (H57-597); anti-CD44 (IM7); anti-CD14 (Sa2-8); anti-CD45 (30-F11); anti-CD62L (MEL-14); anti-CD209 (5H10); anti-CD20 (2H7); anti-IFNγ (XMG1.2); anti-TNF-α (MP6-XT22); anti-FoxP3 (FJK-16s); and anti-IL-6 (MP5-20F3). Anti-CD8a-VioBlue was purchased from Miltenyi Biotech. Antibodies made in-house include: anti-CD4 (GK1.5); anti-CD40 (1C10); anti-CD25 (PC61.5.3); anti-CD5 (53-7.313); and anti-CD3 (145-2C11). Single cell suspensions were incubated on ice with appropriate antibodies for 30 min. Cells were washed with running buffer 3 times fixed in 1% paraformaldehyde/PBS, and then suspended in running buffer for flow cytometry. Results were analyzed with FlowJo software.
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2

Immunohistochemical Staining of Mouse Uterine Tissue

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Frozen section (8 μm) of mouse uterine tissue was fixed in pre-cold cooled methanol for 10 min., Then, after the tissue was incubated with 0.3% H2O2 for 10 min at room temperature, and the slides were blocked in 5% bovine serum albumin (BSA) (Invitrogen, CA) for 1 h at 37 °C. Next, the sections were incubated with anti-Ly-6G (RB6-8C5; eBiosciences, San Diego, CA, USA) diluted in PBS (1:500) overnight at 4 °C. Then, the sections were incubated with a secondary antibody conjugated to HRP at 37 °C for 1 h. Finally, the slides were stained with diaminobenzidine and counterstained with haematoxylin, and then observed and photographed using a Nikon H600L (Japan) microscope.
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